Dr. Miguel  A. Yus Astiz
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Dr. Miguel A. Yus Astiz

Professor
University of Alicante, Spain


Highest Degree
Ph.D. in Organic Chemistry from University of Zaragoza, Spain

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Biography

Dr. Miguel A. Yus Astiz holds a position of Professor in Organic Chemistry at University of Alicante, Spain. He earned his Ph.D. in Organic Chemistry from University of Zaragoza, Spain, and Postdoctoral Fellow at the Max Planck Institut fur Kohlenforschung in Mulheim ad Ruhr. His area of expertise includes Organic Chemistry, Active Metals in Synthesis, Organic Synthesis, Organolithium Compounds, Asymmetric Catalysis, Organomagnesium Compounds, Nanoparticles in Synthesis, and Organozinc Compounds. In 1988 he moved to a chair in Organic Chemistry at the University of Alicante, Visiting Professor at ETH-Zentrum, Oxford, Harvard, Uppsala, Tucson, Okayama, Paris, Strasbourg and Kyoto. He is a co-author of more than 400 papers mainly in the field of the development of new Methodologies Involving Organometallic Intermediates, and three patents. He is member of advisory board in Tetrahedron, Tetrahedron Letters, Chemistry Letters, and European Journal of Organic Chemistry, Trends in Organic Chemistry, Current Organic Chemistry and Current Chemical Biology, being Past Regional Editor of Letters in Organic Chemistry. He has supervised 45 PhD students. Dr. Miguel received honors include Japan Society for the Promotion of Science Prize, the French-Spanish Prize of the Societe Francaise de Chimie, the CA Stiefvater Memorial Lecture Award, the Nagase Science and Technology Foundation fellowship, the Cellchem Lectureship, the Singenta Lectureship and the Fundeun-Iberdrola Prize. His current research interest is focused on the preparation of very reactive Functionalized Organometallic Compounds and their use in Synthetic Organic Chemistry, Arene-Catalyzed Activation of different metals, preparation of new Metal-Based Catalysts, Treats including Metallic Nanoparticles, for Homogeneous and Heterogeneous reactions and selective Asymmetric Catalysis.

Area of Interest:

Molecular Sciences
100%
Organic Chemistry
62%
Organic Synthesis
90%
Organolithium Compounds
75%
Organozinc Compounds
55%

Research Publications in Numbers

Books
0
Chapters
0
Articles
197
Abstracts
0

Selected Publications

  1. Sirvent, A., M.J. GarcØa-MuÜoz, M. Yus and F. Foubelo, 2020. Stereoselective synthesis of tetrahydroisoquinolines from chiral 4-azaocta-1,7-diynes and 4-azaocta-1,7-enynes. Eur. J. Org. Chem., 2020: 113-126.
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  2. HernÌndez-IbÌÜez, S., O.S. do Rego Barros, A. Lahosa, M.J. GarcØa-MuÜoz, M. Benlahrech, C. Behloul, F. Foubelo and M. Yus, 2020. Stereoselective synthesis of 5-(1-aminoalkyl)-2-pyrrolidones and 1,7-diazaspiro[4.5]decane-2,8-diones from chiral N-tert-butanesulfinyl imines and ethyl 4-nitrobutanoate. Tetrahedron, Vol. 76. 10.1016/j.tet.2019.130842.
    CrossRef  |  Direct Link  |  
  3. Yus, M., F. Foubelo and E. MaciÌ, 2019. Indium mediated allylation of N-tert-butanesulfinyl imines with 1,3-dibromopropene: stereoselective synthesis of aziridines. Heterocycles, 99: 248-266.
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  4. NÌjera, C., L.K. Sydnes and M. Yus, 2019. Conjugated ynones in organic synthesis. Chem. Rev., 119: 11110-11244.
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  5. NÌjera, C., I.P. Beletskaya and M. Yus, 2019. Metal-catalyzed regiodivergent organic reactions. Chem. Soc. Rev., 48: 4515-4618.
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  6. Mendes, J.A., P. Merino, T. Soler, E.J. Salustiano and P.R.R. Costa et al., 2019. Enantioselective synthesis, DFT calculations, and preliminary antineoplastic activity of dibenzo 1-azaspiro[4.5]decanes on drug-resistant leukemias. J. Org. Chem., 84: 2219-2233.
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  7. Lahosa, A., M. Yus and F. Foubelo, 2019. Enantiodivergent approach to the synthesis of Cis-2,6-Disubstituted piperidin-4-ones. J. Org. Chem., 84: 7331-7341.
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  8. Yus, M., C. Behloul, F. Foubelo, M. Benlahrech and A. Lahosa, 2018. Highly convergent straightforward stereoselective synthesis of (+)-C(9a)-epiepiquinamide. Heterocycles, 97: 1191-1202.
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  9. Ikhlef, S., C. Behloul, A. Lahosa, F. Foubelo and M. Yus, 2018. Direct access to N-tert-butanesulfinyl imines from aryl iodides, alkenyl alcohols, and N-tert-Butanesulfinamide. Eur. J. Org. Chem., 2018: 2609-2614.
    CrossRef  |  Direct Link  |  
  10. Najera, C. and M. Yus, 2015. Chiral benzimidazoles as hydrogen bonding organocatalysts. Tetrahedron Lett., 56: 2623-2633.
    CrossRef  |  
  11. Garcia-Munoz, M.J., F. Foubelo and M. Yus, 2015. Stereoselective aza-henry reaction of chiral tert-butanesulfinyl imines with methyl or ethyl 4-nitrobutanoate: easy access to enantioenriched 6-substituted piperidine-2, 5-diones (dedicated to professor isao kuwajima on the occasion of his 77th birthday). Heterocycles, 90: 1419-1432.
    Direct Link  |  
  12. Behloul, C., A. Chouti, D. Guijarro, C. Najera and M. Yus, 2015. Reductive removal of the pivaloyl protecting group from tetrazoles by a naphthalene-catalyzed lithiation process. Synth., 47: 507-510.
    Direct Link  |  
  13. do Rego Barros, O.S., J.A. Sirvent, F. Foubelo and M. Yus, 2014. Diastereoselective allylation and crotylation of N-tert-butanesulfinyl imines with allylic alcohols. Chem. Commun., 50: 6898-6901.
    Direct Link  |  
  14. Sirvent, J.A., F. Foubelo and M. Yus, 2014. Enantioselective synthesis of tetrahydroquinoline alkaloids (-)-angustureine and (-)-cuspareine from chiral tert-butanesulfinyl imines (dedicated to professor victor snieckus on the occasion of his 77th birthday). Heterocycles, 88: 1163-1174.
    Direct Link  |  
  15. Planellas, M., Y. Moglie, F. Alonso, M. Yus, R. Pleixats and A. Shafir, 2014. Heck, sonogashira, and hiyama reactions catalyzed by palladium nanoparticles stabilized by tris-imidazolium salt. Eur. J. Org. Chem., 2014: 3001-3008.
    CrossRef  |  
  16. Planellas, M., W. Guo, F. Alonso, M. Yus, A. Shafir, R. Pleixats and T. Parella, 2014. Hydrosilylation of internal alkynes catalyzed by tris-imidazolium salt-stabilized palladium nanoparticles. Adv. Synth. Catal., 356: 179-188.
    CrossRef  |  
  17. Pablo, O., D. Guijarro and M. Yus, 2014. Microwave-enhanced asymmetric transfer hydrogenation of n-(tert-butylsulfinyl) imines. Eur. J. Org. Chem., 2014: 7034-7038.
    CrossRef  |  
  18. Martinez, R., I.M. Pastor and M. Yus, 2014. Enantioselective catalytic lithiation using a chiral binaphthyl derivative as electron carrier. Arkivoc, 2: 71-84.
  19. Martinez, R., I.M. Pastor and M. Yus, 2014. 1, 2-Functionalized imidazoles as palladium ligands: an efficient and robust catalytic system for the fluorine-free hiyama reaction. Eur. J. Org. Chem., 2014: 872-877.
    CrossRef  |  
  20. Martinez Flores, R., I.M. Pastor Bevia and M. Yus Astiz, 2014. Biscarboxy-functionalized imidazole and palladium as highly active catalytic system in protic solvents: methanol and water. Synth., 46: 2965-2975.
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  21. Garcia-Munoz, M.J., H.K. Dema, F. Foubelo and M. Yus, 2014. Base-promoted diastereoselective addition of nitromethane and nitroethane to N-tert-butylsulfinyl imines: synthesis of N-protected α-amino acids and amino ketones. Tetrahedron: Asymmetry, 25: 362-372.
    CrossRef  |  
  22. Foubelo, F. and M. Yus, 2014. Diastereoselective indium-promoted allylation of chiral n-sulfinyl imines. Eur. J. Org. Chem., 2014: 485-491.
    CrossRef  |  
  23. Fernandez-Mateos, E., B. Macia and M. Yus, 2014. Catalytic enantioselective addition of aryl grignard reagents to ketones. Eur. J. Org. Chem., 2014: 6519-6526.
    CrossRef  |  
  24. Behloul, C., K. Bouchelouche, D. Guijarro, C. Najera and M. Yus, 2014. Detritylation of protected tetrazoles by naphthalene-catalyzed lithiation. Synth., 46: 2065-2070.
    Direct Link  |  
  25. Yus, M., J.C. Gonzalez-Gomez and F. Foubelo, 2013. Diastereoselective allylation of carbonyl compounds and imines: application to the synthesis of natural products. Chem. Rev., 113: 5595-5698.
    Direct Link  |  
  26. Yus, M. and I.M. Pastor, 2013. Heterocyclic carbene�metal-catalyzed Csp 2�Csp 2 and Csp�Csp 2 couplings using nonmetallic substrates. Chem. Lett., 42: 94-108.
  27. Yus, M. F. Foubelo and J.V. Ferrandez, 2013. Dibenzothiepins, phtalans and pthalides from 4-heterosubstituted dibezothiins. Tetrahedron, 59: 2083-2092.
  28. Sirvent, J.A., F. Foubelo and M. Yus, 2013. Chiral aminated α-methylenebenzocycloalkenes from o-bromoaryl aldehydes and ketones. Eur. J. Org. Chem., 2013: 2461-2471.
    CrossRef  |  
  29. Penafiel, I., I.M. Pastor and M. Yus, 2013. NHC-Ligand effectiveness in the fluorine-free hiyama reaction of aryl halides. Eur. J. Org. Chem., 2013: 1479-1484.
    CrossRef  |  
  30. Pablo, O., D. Guijarro and M. Yus, 2013. Synthesis of nitrogenated heterocycles by asymmetric transfer hydrogenation of n-(tert-butylsulfinyl) haloimines. J. org. chem., 78: 9181-9189.
    Direct Link  |  
  31. Guijarro, D., O. Pablo and M. Yus, 2013. Synthesis of highly enantiomerically enriched amines by asymmetric transfer hydrogenation of n-(tert-butylsulfinyl) imines. Org. Synth., 90: 338-349.
    CrossRef  |  
  32. Guijarro, D., O. Pablo and M. Yus, 2013. Synthesis of γ-, δ-, and ε-lactams by asymmetric transfer hydrogenation of N-(tert-Butylsulfinyl) iminoesters. J. org. chem., 78: 3647-3654.
    Direct Link  |  
  33. Garcia-Munoz, M.J., F. Zacconi, F. Foubelo and M. Yus, 2013. Indium-promoted diastereo-and regioselective propargylation of chiral sulfinylimines. Eur. J. Org. Chem., 2013: 1287-1295.
    CrossRef  |  
  34. Fernandez-Mateos, E., B. Macia and M. Yus, 2013. Catalytic enantioselective addition of alkyl grignard reagents to aliphatic aldehydes. Adv. Synth. Catal., 355: 1249-1254.
    CrossRef  |  
  35. Cano, R., M. Yus and D.J. Ramon, 2013. Environmentally friendly and regioselective C 3-alkylation of indoles with alcohols through a hydrogen autotransfer strategy. Tetrahedron Lett., 54: 3394-3397.
  36. Cano, R., M. Yus and D.J. Ramon, 2013. Catalyzed addition of acid chlorides to alkynes by unmodified nano-powder magnetite: synthesis of chlorovinyl ketones, furans, and related cyclopentenone derivatives. Tetrahedron, 69: 7056-7065.
    CrossRef  |  
  37. Buil, M.L., M.A. Esteruelas, J. Herrero, S. Izquierdo, I.M. Pastor and M. Yus, 2013. Osmium catalyst for the borrowing hydrogen methodology: α-alkylation of arylacetonitriles and methyl ketones. ACS Catal., 3: 2072-2075.
  38. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2013. Alkenes as azido precursors for the one-pot synthesis of 1, 2, 3-triazoles catalyzed by copper nanoparticles on activated carbon. J. org. chem., 78: 5031-5037.
    Direct Link  |  
  39. Almansa, R., J.F. Collados, D. Guijarro and M. Yus, 2013. Polymer-supported l-prolinol-based catalysts for the enantioselective addition of dialkylzinc reagents to N-(diphenylphosphinyl)imines. Tetrahedron Asymmetry, 24: 116-120.
    CrossRef  |  
  40. Albaladejo, M.J., F. Alonso and M. Yus, 2013. Synthesis of indolizines and heterocyclic chalcones catalyzed by supported copper nanoparticles. Chem. A Eur. J., 19: 5242-5245.
  41. Abdulkin, P., Y. Moglie, B.R. Knappett, D.A. Jefferson, M. Yus, F. Alonso and A.E. Wheatley, 2013. New routes to Cu (I)/Cu nanocatalysts for the multicomponent click synthesis of 1, 2, 3-triazoles. Nanoscale, 5: 243-350.
    Direct Link  |  
  42. Sirvent, J.A., F. Foubelo and M. Yus, 2012. Diastereoselective indium-mediated allylation of N-tert-butanesulfinyl ketimines: easy access to asymmetric quaternary stereocenters bearing nitrogen atoms. Chem. Commun., 48: 2543-2545.
    Direct Link  |  
  43. Perez, J.M., R. Cano, M. Yus and D.J. Ramon, 2012. Straightforward synthesis of aromatic imines from alcohols and amines or nitroarenes using an impregnated copper catalyst. Eur. J. Org. Chem., 2012: 4548-4554.
    CrossRef  |  
  44. Penafiel, I., I.M. Pastor, M. Yus, M.A. Esteruelas and M. Olivan, 2012. Preparation, hydrogen bonds, and catalytic activity in metal-promoted addition of arylboronic acids to enones of a rhodium complex containing an nhc ligand with an alcohol function. Organomet., 31: 6154-6161.
    Direct Link  |  
  45. Penafiel, I., I.M. Pastor and M. Yus, 2012. Heck�matsuda reactions catalyzed by a hydroxyalkyl-functionalized NHC and palladium acetate. Eur. J. Org. Chem., 2012: 3151-3156.
    CrossRef  |  
  46. Pastor, I.M., and M. Yus, 2012. Focused update on the prins reaction and the prins cyclization. Curr. Org. Chem., 16: 1277-1312.
    Direct Link  |  
  47. Pablo, O., D. Guijarro, G. Kovacs, A. Lledos, G. Ujaque and M. Yus, 2012. A versatile Ru catalyst for the asymmetric transfer hydrogenation of both aromatic and aliphatic sulfinylimines. Chem. A Eur. J., 18: 1969-1983.
    CrossRef  |  
  48. Pablo, O., D. Guijarro and M. Yus, 2012. Chiral β-amino alcohols as ligands for the ruthenium-catalyzed asymmetric transfer hydrogenation of n-phosphinyl ketimines. Appl. Sci., 2: 1-12.
    Direct Link  |  
  49. Nador, F., Y. Moglie, A. Ciolino, A. Pierini, V. Dorn, M. Yus and G. Radivoy, 2012. Direct reductive amination of aldehydes using lithium-arene (cat.) as reducing system. A simple one-pot procedure for the synthesis of secondary amines. Tetrahedron Lett., 53: 3156-3160.
    CrossRef  |  
  50. Medjahdi, M., J.C. Gonzalez-Gomez and F. Foubelo, 2012. Enantioselective synthesis of CIS-AND Trans-2-Methyl-6-Nonylpiperidines: alkaloids solenopsin and isosolenopsin (Dedicated to Professor Dr. Ei-ichi Negishi on the occasion of his 77th birthday). Heterocycles, 86: 727-734.
  51. Martinez-Asencio, A., M. Yus and D.J. Ramon, 2012. Copper (II) acetate-catalyzed one-pot conversion of aldehydes into primary amides through a Beckmann-type rearrangement. Tetrahedron, 68: 3948-3951.
    CrossRef  |  
  52. Martinez, R., R. Torregrosa, I.M. Pastor and M. Yus, 2012. Isoprene as lithiation mediator: synthesis of 2-substituted 1-alkylimidazole derivatives. Synth., 2012: 2630-2638.
    Direct Link  |  
  53. Gonzalez-Lopez, S., M. Yus and D.J. Ramon, 2012. Enantioselective synthesis of (+)-gossonorol and related systems using organozinc reagents. Tetrahedron: Asymmetry, 23: 611-615.
    CrossRef  |  
  54. Gonzalez-Gomez, J., F. Foubelo and M. Yus, 2012. Preparation of enantioenriched homoallylic primary amines. Org. Synth., 89: 88-97.
    CrossRef  |  
  55. Fernandez-Mateos, E., B. Macia and M. Yus, 2012. Catalytic enantioselective addition of organoaluminum reagents to aldehydes. Tetrahedron: Asymmetry, 23: 789-794.
    CrossRef  |  
  56. Fernandez-Mateos, E., B. Macia and M. Yus, 2012. Catalytic asymmetric addition of alkyllithium reagents to aromatic aldehydes. Eur. J. Org. Chem., 2012: 3732-3736.
    Direct Link  |  
  57. Dema, H.K., F. Foubelo and M. Yus, 2012. Diastereoselective coupling of n-(tert-butyl) sulfinyl imines and dimethyl malonate. Synthesis of enantiomerically enriched β-amino esters and β-lactams. Helv. Chim. Acta, 95: 1790-1798.
    Direct Link  |  
  58. Collados, J.F., E. Toledano, D. Guijarro and M. Yus, 2012. Microwave-assisted solvent-free synthesis of enantiomerically pure N-(tert-Butylsulfinyl) imines. J. org. chem., 77: 5744-5750.
    Direct Link  |  
  59. Cano, R., M. Yus and D.J. Ramon, 2012. Impregnated platinum on magnetite as an efficient, fast, and recyclable catalyst for the hydrosilylation of alkynes. ACS Catal., 2: 1070-1078.
    CrossRef  |  
  60. Cano, R., M. Yus and D.J. Ramon, 2012. Impregnated copper or palladium�copper on magnetite as catalysts for the domino and stepwise Sonogashira-cyclization processes: a straightforward synthesis of benzo [b] furans and indoles. Tetrahedron, 68: 1393-1400.
    CrossRef  |  
  61. Cano, R., M. Yus and D.J. Ramon, 2012. First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chem. Commun., 48: 7628-7630.
    CrossRef  |  
  62. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2012. Solvent-and catalyst-free regioselective hydrophosphanation of alkenes. Green Chem., 14: 2699-2702.
    Direct Link  |  
  63. Alonso, F., R. Buitrago, Y. Moglie, A. Sepulveda-Escribano and M. Yus, 2012. Selective hydrosilylation of 1, 3-diynes catalyzed by titania-supported platinum. Organomet., 31: 2336-2342.
    Direct Link  |  
  64. Alonso, F. and M. Yus, 2012. Heterogeneous catalytic homocoupling of terminal alkynes. ACS Catal., 2: 1441-1451.
    Direct Link  |  
  65. Alonso Valdes, F., Y. Moglie, G. Radivoy and M. Yus Astiz, 2012. Copper-catalysed multicomponent click synthesis of 5-alkynyl 1, 2, 3-triazoles under ambient conditions. Synlett., 23: 2179-2182.
    Direct Link  |  
  66. Albaladejo, M.J., F. Alonso, Y. Moglie and M. Yus, 2012. Three-component coupling of aldehydes, amines, and alkynes catalyzed by oxidized copper nanoparticles on titania. Eur. J. Org. Chem., 2012: 3093-3104.
    Direct Link  |  
  67. de la Viuda, M., M. Yus and A. Guijarro, 2011. On the nature of lithium biphenyl in ethereal solvents. a critical analysis unifying dft calculations, physicochemical data in solution, and a x-ray structure. J. Phys. Chem. B, 115: 14610-14616.
  68. Yus, M., J.C. Gonzalez-Gomez and F. Foubelo, 2011. Catalytic enantioselective allylation of carbonyl compounds and imines. Chem. Rev., 111: 7774-7854.
    Direct Link  |  
  69. Yus, M., 2011. Discovering new arene-catalyzed lithiations. Contrib. Sci., 6: 155-160.
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  70. Tari, S., R. Chinchilla, C. Najera, M. Yus and O.S. Giordano, 2011. Enantioselective alkylation of β-keto esters promoted by dimeric cinchona-derived ammonium salts as recoverable organocatalysts. Arkivoc, 7: 116-127.
  71. Penafiel, I., I.M. Pastor, M. Yus, M.A. Esteruelas, M. Olivan and E. Onate, 2011. (NHC) Palladium complexes from hydroxy-functionalized imidazolium salts as catalyst for the microwave-accelerated fluorine-free hiyama reaction. Eur. J. Org. Chem., 2011: 7174-7181.
  72. Medjahdi, M., J.C. Gonzalez-Gomez, F. Foubelo and M. Yus, 2011. Concise route to (�)-and (+)-aphanorphine. Eur. J. Org. Chem., 2011: 2230-2234.
    CrossRef  |  
  73. Martinez-Asencio, A., M. Yus and D.J. Ramon, 2011. Palladium (II) acetate as catalyst for the n-alkylation of aromatic amines, sulfonamides, and related nitrogenated compounds with alcohols by a hydrogen autotransfer process. Synth., 2011: 3730-3740.
    Direct Link  |  
  74. Martinez-Asencio, A., D.J. Ramon and M. Yus, 2011. N-Alkylation of poor nucleophilic amines and derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper (II) acetate: scope and mechanistic considerations. Tetrahedron, 67: 3140-3149.
    CrossRef  |  
  75. Guijarro, D., O. Pablo and M. Yus, 2011. Achiral β-amino alcohols as efficient ligands for the ruthenium-catalysed asymmetric transfer hydrogenation of sulfinylimines. Tetrahedron Lett., 52: 789-791.
    CrossRef  |  
  76. Guijarro, D., I.M. Pastor and M. Yus, 2011. Non-deprotonating methodologies for organolithium reagents starting from non-halogenated materials. part 2: transmetallation and addition to multiple bonds. Curr. Org. Chem., 15: 2362-2389.
  77. Guijarro, D., I.M. Pastor and M. Yus, 2011. Non-deprotonating methodologies for organolithium reagents starting from non-halogenated materials. part 1: carbon-heteroatom bond cleavage. Curr. Org. Chem., 15: 375-400.
  78. Guijarro, A., M.de la Viuda, R. Torregrosa, I. Penafiel, I.M. Pastor, M. Yus and C. Najera, 2011. Isoprene-mediated lithiation of imidazole derivatives: mechanistic considerations. Arkivoc, 5: 12-22.
  79. Fernandez-Mateos, E., B. Macia, D.J. Ramon and M. Yus, 2011. Catalytic enantioselective addition of MeMgBr and other Grignard reagents to aldehydes. Eur. J. Org. Chem., 2011: 6851-6855.
    Direct Link  |  
  80. Eguillor, B., M.A. Esteruelas, J. Garcia-Raboso, M. Olivan, E. Onate, I.M. Pastor and M. Yus, 2011. Osmium NHC complexes from alcohol-functionalized imidazoles and imidazolium salts. Organomet., 30: 1658-1667.
    Direct Link  |  
  81. Dema, H.K., F. Foubelo and M. Yus, 2011. Indium�mediated Allylation of N�tert�Butylsulfinylaldimines with Dimethyl 2�[2�(Chloromethyl) allyl] malonate. Jordan J. Chem., 6: 247-255.
  82. Dema, H.K., F. Foubelo and M. Yus, 2011. Enantioselective synthesis of α-methylene-γ-butyrolactams using N-tert-butanesulfinamides. Heterocycles, 82: 1411-1421.
    Direct Link  |  
  83. Cano, R., M. Yus and D.J. Ramon, 2011. Impregnated palladium on magnetite as catalyst for multicomponent reductive amination reactions and other related reducing processes. Tetrahedron, 67: 8079-8085.
    CrossRef  |  
  84. Cano, R., D.J. Ramon and M. Yus, 2011. Unmodified nano-powder magnetite or iron (iii) oxide catalyze the easy and fast synthesis of 4-substituted-4h-pyrans. Synlett., 2011: 2017-2020.
    Direct Link  |  
  85. Cano, R., D.J. Ramon and M. Yus, 2011. Impregnated ruthenium on magnetite as a recyclable catalyst for the N-alkylation of amines, sulfonamides, sulfinamides, and nitroarenes using alcohols as electrophiles by a hydrogen autotransfer process. J. org. chem., 76: 5547-5557.
    Direct Link  |  
  86. Cano, R., D.J. Ramon and M. Yus, 2011. Impregnated palladium on magnetite, a new catalyst for the ligand-free cross-coupling Suzuki�Miyaura reaction. Tetrahedron, 67: 5432-5436.
    CrossRef  |  
  87. Bosque, I., J.C. Gonzalez-Gomez, F. Foubelo and M. Yus, 2011. Straightforward access to enantioenriched 2-allylpiperidine: application to the synthesis of alkaloids. J. org. chem., 77: 780-784.
    Direct Link  |  
  88. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2011. Multicomponent click synthesis of potentially biologically active triazoles catalysed by copper nanoparticles on activated carbon in water. Heterocycles, 84: 1033-1044.
    Direct Link  |  
  89. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2011. Multicomponent click synthesis of 1, 2, 3-triazoles from epoxides in water catalyzed by copper nanoparticles on activated carbon. J. org. chem., 76: 8394-8405.
    Direct Link  |  
  90. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2011. Click chemistry from organic halides, diazonium salts and anilines in water catalysed by copper nanoparticles on activated carbon. Org. biomol. Chem., 9: 6385-6395.
    Direct Link  |  
  91. Alonso, F., T. Melkonian, Y. Moglie and M. Yus, 2011. Homocoupling of terminal alkynes catalysed by ultrafine copper nanoparticles on titania. Eur. J. Org. Chem., 2011: 2524-2530.
    CrossRef  |  
  92. Alonso, F., R. Buitrago, Y. Moglie, J. Ruiz-Martinez, A. Sepulveda-Escribano and M. Yus, 2011. Hydrosilylation of alkynes catalysed by platinum on titania. J. Organomet. Chem., 696: 368-372.
    CrossRef  |  
  93. Alonso, F., P. Riente and M. Yus, 2011. Nickel nanoparticles in hydrogen transfer reactions. Acc. Chem. Res., 44: 379-391.
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  94. Alonso, F., M. Rodriguez-Fernandez, D. Sanchez, and M. Yus, 2011. Synthesis of perhydrofuro [2, 3-b] furans from isopentenyl alcohol through carbonyl-ene and wacker-type reactions. Eur. J. Org. Chem., 2011: 6459-6469.
    CrossRef  |  
  95. Penafiel, I., I.M. Pastor and M. Yus, 2010. Cyclopropylmethyl-and cyclobutylmethyllithium by an arene-catalyzed lithiation. Stability and reactivity. Tetrahedron, 66: 2928-2935.
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  96. Pastor, M.I., R. Torregrosa and M. Yus, 2010. Isoprene-mediated lithiation of 1-alkylimidazoles: chiral induction of the alkyl substituent. Lett. Org. Chem., 7: 373-376.
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  97. Najera, C., J.M. Sansano and M. Yus, 2010. Metal complexes versus organocatalysts in asymmetric 1, 3-dipolar cycloadditions. J. Bra. Chem. Soc., 21: 377-412.
  98. Nador, F., Y. Moglie, C. Vitale, M. Yus, F. Alonso and G. Radivoy, 2010. Reduction of polycyclic aromatic hydrocarbons promoted by cobalt or manganese nanoparticles. Tetrahedron, 66: 4318-4325.
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  99. Martinez-Asencio, A., D.J. Ramon and M. Yus, 2010. N-Alkylation of poor nucleophilic amine and sulfonamide derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper (II) acetate. Tetrahedron Lett., 51: 325-327.
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  100. Lillo, V.J., C. Gomez and M. Yus, 2010. A 1, 3-sp2, sp3-hybridized dilithio intermediate by direct lithiation of cyclopropylidene diphenylmethane. Arkivoc, 3: 29-44.
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  102. Gonzalez-Gomez, J.C., M. Medjahdi, F. Foubelo and M. Yus, 2010. Stereoselective α-aminoallylation of aldehydes with chiral tert-butanesulfinamides and allyl bromides. J. org. chem., 75: 6308-6311.
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  103. Garcia, D., F. Foubelo and M. Yus, 2010. Reductive ring-opening of phthalan and isochroman: Application to the stereoselective synthesis of tetrahydroisoquinolines and tetrahydrobenzazepines. Eur. J. Org. Chem., 2010: 2893-2903.
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  104. Dema, H.K., F. Foubelo and M. Yus, 2010. Stereoselective synthesis of α-methylene-y-butyrolactams from ethyl 2-(bromomethyl) acrylate and chiral sulfinyl aldimines mediated by indium. Heterocycles, 80: 125-131.
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  105. Cano, R., D.J. Ramon and M. Yus, 2010. Transition-metal-free O-, S-, and N-arylation of alcohols, thiols, amides, amines, and related heterocycles. J. org. chem., 76: 654-660.
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  106. Cano, R., D.J. Ramon and M. Yus, 2010. Impregnated copper on magnetite as recyclable catalyst for the addition of alkoxy diboron reagents to c− c double bonds. J. org. chem., 75: 3458-3460.
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  107. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2010. Unsupported copper nanoparticles in the 1, 3-dipolar cycloaddition of terminal alkynes and azides. Eur. J. org. chem., 2010: 1875-1884.
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  108. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2010. Multicomponent synthesis of 1, 2, 3-triazoles in water catalyzed by copper nanoparticles on activated carbon. Adv. Synth. Catal., 352: 3208-3214.
  109. Alonso, F., P. Riente, J.A. Sirvent and M. Yus, 2010. Nickel nanoparticles in hydrogen-transfer reductions: Characterisation and nature of the catalyst. Applied Catal. A: Gen., 378: 42-51.
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  110. Alonso, F., F. Foubelo, J.C. Gonzalez-Gomez, R. Martinez, D.J. Ramon, P. Riente and M. Yus, 2010. Efficiency in chemistry: from hydrogen autotransfer to multicomponent catalysis. Mol. diversity, 14: 411-424.
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  111. Alonso, D.A., C. Najera, I.M. Pastor and M. Yus, 2010. Transition-metal-catalyzed synthesis of hydroxylated arenes. Chem. A Eur. J., 16: 5274-5284.
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  112. Almansa, R., J.F. Collados, D. Guijarro and M. Yus, 2010. Asymmetric synthesis of α-and β-amino acids by diastereoselective addition of triorganozincates to N-(tert-butanesulfinyl) imines. Tetrahedron: Asymmetry, 21: 1421-1431.
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  113. Aliaga, M.J., D.J. Ramon and M. Yus, 2010. Impregnated copper on magnetite: an efficient and green catalyst for the multicomponent preparation of propargylamines under solvent free conditions. Org. biomol. Chem., 8: 43-46.
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  114. Perez, H., C. Melero, A. Guijarro and M. Yus, 2009. The reaction of biphenyl radical anion and dianion with alkyl fluorides. From ET to S N 2 reaction pathways and synthetic applications. Tetrahedron, 65: 10769-10783.
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  115. Melero, C., A. Guijarro and M. Yus, 2009. Structural characterization and bonding properties of lithium naphthalene radical anion,[Li+(TMEDA) 2][C 10 H 8˙−], and lithium naphthalene dianion [(Li+ TMEDA) 2 C 10 H 8− 2]. Dalton Trans., 2009: 1286-1289.
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  116. Medjahdi, M., J.C. Gonzalez-Gomez, F. Foubelo and M. Yus, 2009. Stereoselective synthesis of azetidines and pyrrolidines from n-tert-butylsulfonyl (2-aminoalkyl) oxiranes. J. org. chem., 74: 7859-7865.
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  117. Martinez, R., D.J. Ramon and M. Yus, 2009. Selective N-monoalkylation of aromatic amines with benzylic alcohols by a hydrogen autotransfer process catalyzed by unmodified magnetite. Org. biomol. Chem., 7: 2176-2181.
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  118. Lillo, V.J., C. Gomez and M. Yus, 2009. 2, 2′-Dilithiobiphenyl by direct lithiation of biphenylene. Tetrahedron Lett., 50: 2266-2269.
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  119. Guillena, G., J. D. Ramon and M. Yus, 2009. Hydrogen autotransfer in the N-alkylation of amines and related compounds using alcohols and amines as electrophiles. Chem. Rev., 110: 1611-1641.
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  120. Guijarro, D., O. Pablo and M. Yus, 2009. Ruthenium-catalysed asymmetric transfer hydrogenation of N-(tert-butanesulfinyl) imines. Tetrahedron Lett., 50: 5386-5388.
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  121. Gonzalez-Gomez, J.C., F. Foubelo and M. Yus, 2009. Stereocontrolled synthesisof 1, 3-amino alcohols by reduction of substituted 2-{1-[(tert-Butylsulfinyl) amino] alkyl} cyclohexanones. Synth., 2009: 2083-2088.
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  122. Gonzalez, J.C., F. Foubelo and M. Yus, 2009. Modular stereocontrolled assembly of r2zn, cyclic enones and N-tert-Butanesulfinyl Imines. J. org. chem., 74: 2547-2553.
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  123. Garcia, D., F. Foubelo and M. Yus, 2009. Selective lithiation of 4-and 5-halophthalans. Heterocycles, 77: 991-1005.
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  124. Garcia, D., B. Moreno, T. Soler, F. Foubelo and M. Yus, 2009. Stereoselective synthesis of 3-substituted tetrahydroisoquinolines from phthalan and chiral N-sulfinylimines. Tetrahedron Lett., 50: 4710-4713.
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  125. Forrat, V.J., D.J. Ramon and M. Yus, 2009. Enantioselective addition of organozinc reagents to ketones catalyzed by grafted isoborneolsulfonamide polymers and titanium isopropoxide. Tetrahedron: Asymmetry, 20: 65-67.
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  126. Alonso, F., Y. Moglie, G. Radivoy and M. Yus, 2009. Copper nanoparticles in click chemistry: an alternative catalytic system for the cycloaddition of terminal alkynes and azides. Tetrahedron Lett., 50: 2358-2362.
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  127. Alonso, F., P. Riente, F. Rodriguez-Reinoso, J. Ruiz-Martinez, A. Sepulveda-Escribano and M. Yus, 2009. A highly reusable carbon-supported platinum catalyst for the hydrogen-transfer reduction of ketones. Chem. Catal. Chem., 1: 75-77.
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  128. Alonso, F., P. Riente and M. Yus, 2009. Wittig-type olefination of alcohols promoted by nickel nanoparticles: synthesis of polymethoxylated and polyhydroxylated stilbenes. Eur. J. Org. Chem., 2009: 6034-6042.
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  129. Alonso, F., P. Riente and M. Yus, 2009. Transfer hydrogenation of olefins catalysed by nickel nanoparticles. Tetrahedron, 65: 10637-10643.
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  130. Alonso, F., P. Riente and M. Yus, 2009. Synthesis of resveratrol, DMU-212 and analogues through a novel wittig-type olefination promoted by nickel nanoparticles. Tetrahedron Lett., 50: 3070-3073.
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  131. Alonso, F., P. Riente and M. Yus, 2009. One-pot synthesis of stilbenesfrom alcohols through a wittig-type olefination reactionpromoted by nickel nanoparticles. Synlett., 2009: 1579-1582.
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  132. Almansa, R., D. Guijarro and M.Yus, 2009. An improved procedure for the diastereoselective addition of triorganozincates to N-(tert-butanesulfinyl) imines: use of catalytic dialkylzinc. Tetrahedron Lett., 50: 3198-3201.
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  133. Torregrosa, R., I.M. Pastor and M. Yus, 2008. Isoprene-promoted lithiation of 1-phenylimidazole. Arkivoc, 7: 8-15.
  134. Pastor, I.M., I. Penafiel and M. Yus, 2008. Easy selective generation of (lithiomethyl) cyclopropane or homoallyllithium by a chlorine�lithium exchange. Tetrahedron Lett., 49: 6870-6872.
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  135. Muller, T.E., K.C. Hultzsch, M. Yus, F. Foubelo and M. Tada, 2008. Hydroamination: direct addition of amines to alkenes and alkynes. Chem. Rev., 108: 3795-3892.
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  136. Medjahdi, M., J.C. Gonzalez-Gomez, F. Foubelo and M. Yus, 2008. Stereoselective synthesis of pyrrolidin-3-ols from homoallylamines. Heterocycles, 76: 569-581.
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  137. Martinez, R., L. Zoli, P.G. Cozzi, D.J. Ramon and M. Yus, 2008. Synthesis of camphorsulfonamide-based quinoline ligands and their N-oxides: first use in the enantioselective addition of organozinc reagents to aldehydes. Tetrahedron: Asymmetry, 19: 2600-2607.
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  138. Martinez, R., D.J. Ramon and M. Yus, 2008. Unmodified nano-powder magnetite catalyzes a four-component aza-sakurai reaction. Adv. Synth. Catal., 350: 1235-1240.
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  139. Martinez, R., D.J. Ramon and M. Yus, 2008. Transition-metal-free indirect friedlander synthesis of quinolines from alcohols. J. org. chem., 73: 9778-9780.
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  140. Lillo, V.J., C. Gomez and M. Yus, 2008. DTBB-Catalysed lithiation of acenaphthylene and reaction with carbonyl compounds. Synth., 2008: 1241-1248.
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  141. Lillo, V.J., C. Gomez and M. Yus, 2008. 1, 3-Dilithio-2-(diphenylmethylene) propane. Tetrahedron Lett., 49: 5182-5185.
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  142. Gonzalez-Gomez, J.C., F. Foubelo and M. Yus, 2008. Tandem enantioselective conjugate addition�Mannich reactions: efficient multicomponent assembly of dialkylzincs, cyclic enones and chiral N-sulfinimines. Tetrahedron Lett., 49: 2343-2347.
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  143. Gonzalez-Gomez, J.C., F. Foubelo and M. Yus, 2008. Cross-Metathesis of Chiral N-tert-ButylsulfinylHomoallylamines: Application to the Enantioselective Synthesis ofNaturally Occurring 2, 6-cis-Disubstituted Piperidines. Synlett., 2008: 2777-2780.
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  144. Garcia, D., F. Foubelo and M. Yus, 2008. Regioselective reductive opening of substituted phthalans: synthetic applications. Tetrahedron, 64: 4275-4286.
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  145. Foubelo, F. and M. Yus, 2008. Functionalised organolithium compounds by sulfur�lithium exchange. Chem. Soc. Rev., 37: 2620-2633.
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  146. Forrat, V.J., D.J. Ramon and M. Yus, 2008. Toward the continuous-flow synthesis of chiral tertiary alcohols by enantioselective addition of organozinc reagents to ketones using nanosize isoborneol ligands. Tetrahedron: Asymmetry, 19: 537-541.
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  147. Alonso, F., P. Riente, F. Rodriguez-Reinoso, J. Ruiz-Martinez, A. Sepulveda-Escribano and M. Yus, 2008. Platinum nanoparticles supported on titania as an efficient hydrogen-transfer catalyst. J. Catal., 260: 113-118.
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  148. Alonso, F., P. Riente and M. Yus, 2008. Hydrogen-transfer reduction of carbonyl compounds promoted by nickel nanoparticles. Tetrahedron, 64: 1847-1852.
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  149. Alonso, F., P. Riente and M. Yus, 2008. Hydrogen-transfer reduction of carbonyl compounds catalysed by nickel nanoparticles. Tetrahedron Lett., 49: 1939-1942.
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  150. Alonso, F., P. Riente and M. Yus, 2008. Homocoupling of aryl iodides promoted by nickel (0) nanoparticles. Arkivoc, 4: 8-15.
  151. Alonso, F., P. Riente and M. Yus, 2008. Alcohols for the α-alkylation of methyl ketones and indirect aza-wittig reaction promoted by nickel nanoparticles. Eur. J. Org. Chem., 2008: 4908-4914.
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  152. Alonso, F., J. Melendez and M. Yus, 2008. A novel route towards the synthesis of spirocyclic bislactones. Synlett, 2008: 1627-1630.
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  153. Alonso, F., I.P. Beletskaya and M. Yus, 2008. Non-conventional methodologies for transition-metal catalysed carbon�carbon coupling: A critical overview. Part 2: The Suzuki reaction. Tetrahedron, 64: 3047-3101.
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  154. Alonso, F., D. Sanchez, T. Soler and M. Yus, 2008. Straightforward synthesis of perhydrofuro [2, 3-b] furans through a wacker-type reaction. Adv. Synth. Catal., 350: 2118-2126.
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  155. Alonso, F. and M. Yus, 2008. New synthetic methodologies based on active transition metals. Pure Appl. Chem., 80: 1005-1012.
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  156. Almansa, R., D. Guijarro and M. Yus, 2008. Triorganozincates as efficient nucleophiles for the diastereoselective addition to N-(tert-butanesulfinyl) imines. Tetrahedron: Asymmetry, 19: 603-606.
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  157. Almansa, R., D. Guijarro and M. Yus, 2008. Synthesis of highly enantiomerically enriched amines by the diastereoselective addition of triorganozincates to N-(tert-butanesulfinyl) imines. Tetrahedron: Asymmetry, 19: 2484-2491.
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  158. Almansa, R., D. Guijarro and M. Yus, 2008. Microwave-accelerated enantioselective addition of dialkylzinc reagents to N-(diphenylphosphinoyl) imines catalysed by β-aminoalcohols with the prolinol skeleton. Tetrahedron: Asymmetry, 19: 1376-1380.
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  159. Torregrosa, R., I.M. Pastor and M. Yus, 2007. Solvent-free direct regioselective ring opening of epoxides with imidazoles. Tetrahedron, 63: 469-473.
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  160. Torregrosa, R., I.M. Pastor and M. Yus, 2007. Isoprene-catalysed lithiation: deprotection and functionalisation of imidazole derivatives. Tetrahedron, 63: 947-952.
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  161. Ramon, D.J. and M. Yus, 2007. Chiral Ligands with an isoborneol-10-sulfonamide structure: A ten-year odyssey. Synlett, 2007: 2309-2320.
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  162. Pastor, I.M. and M. Yus, 2007. The Prins reaction: advances and applications. Curr. Org. Chem., 11: 925-957.
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  163. Melero, C., R.P. Herrera, A. Guijarro and M. Yus, 2007. New modes of reactivity in the threshold of the reduction potential in solution. Alkylation of lithium PAH (polycyclic aromatic hydrocarbon) dianions by primary fluoroalkanes: a reaction pathway complementing the classical Birch reductive alkylation. Chem. A Eur. J., 13: 10096-10107.
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  164. Melero, C., H. Perez, A. Guijarro and M. Yus, 2007. Reductive dearomatization of biphenyl: sequential one-pot regioselective introduction of two different electrophiles. Tetrahedron lett., 48: 4105-4109.
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  165. Melero, C., A. Guijarro, V. Baumann, A.J. Perez-Jimenez and M. Yus, 2007. Carbolithiation of simple terminal and strained internal alkenes by the naphthalene and the biphenyl dianion: new modes of reactivity of highly reduced organic species in solution. Eur. J. Org. Chem., 2007: 5514-5526.
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  166. Martinez, R., D.J. Ramon and M. Yus, 2007. RuCl2 (dmso) 4 catalyzes the solvent-free indirect friedl?nder synthesis of polysubstituted quinolines from alcohols. Eur. J. org. chem., 2007: 1599-1605.
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  167. Guillena, G., D.J. Ramon and M. Yus, 2007. Organocatalytic enantioselective multicomponent reactions (OEMCRs). Tetrahedron: Asymmetry, 18: 693-700.
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  168. Guillena, G., D.J. Ramon and M. Yus, 2007. Alcohols as electrophiles in C- C bond-forming reactions: the hydrogen autotransfer process. Angew. Chem. Int. Ed., 46: 2358-2364.
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  169. Gomez, C., V.J. Lillo and M. Yus, 2007. Arene-catalysed lithiation of phenyl-and 1, 1-diphenylcyclopropane: synthetic applications. Tetrahedron, 63: 4655-4662.
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  170. Garcia, D., F. Foubelo and M. Yus, 2007. Cyclic acetals as precursors of substituted isochromans and naphthoxepines. Heterocycles, 74: 507-519.
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  171. Foubelo, F., D. Garcia, B. Moreno and M. Yus, 2007. Regiochemistry in the reductive opening of phthalan derivatives. Tetrahedron lett., 48: 3379-3383.
  172. Forrat, V.J., D.J. Ramon and M. Yus, 2007. First catalytic enantioselective synthesis of the cocaine abuse therapeutic agent (S)-(+)-1-(4-{2-[bis (4-fluorophenyl) methoxy] ethyl} piperazin-1-yl)-2-phenyl-2-propanol. Tetrahedron: Asymmetry, 18: 400-405.
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  173. Chinchilla, R., C. Najera and M. Yus, 2007. Metalated heterocycles in organic synthesis: recent applications. Arkivoc, 10: 152-231.
  174. Alonso, F., P. Riente and M. Yus, 2007. The α-alkylation of methyl ketones with primary alcohols promoted by nickel nanoparticles under mild and ligandless conditions. Synlett, 2007: 1877-1880.
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  175. Alonso, F., I. Osante and M. Yus, 2007. Highly selective hydrogenation of multiple carbon�carbon bonds promoted by nickel (0) nanoparticles. Tetrahedron, 63: 93-102.
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  176. Alonso, F., F. Foubelo and M. Yus, 2007. 1, 5-Dioxaspiro [2.4] heptanes. Curr. Chem. Biol., 1: 317-346.
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  177. Almansa, R., D. Guijarro and M. Yus, 2007. Nickel-catalysed addition of dialkylzinc reagents to N-phosphinoyl-and N-sulfonylimines. Tetrahedron, 63: 1167-1174.
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  178. Almansa, R., D. Guijarro and M. Yus, 2007. N-Benzyl-l-prolinol: an efficient catalyst for the enantioselective addition of dialkylzinc reagents to N-(diphenylphosphinoyl) imines. Tetrahedron: Asymmetry, 18: 896-899.
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  179. Almansa, R., D. Guijarro and M. Yus, 2007. Enantioselective addition of dialkylzinc reagents to N-(diphenylphosphinoyl) imines catalyzed by β-aminoalcohols with the prolinol skeleton. Tetrahedron: Asymmetry, 18: 2828-2840.
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  180. Almansa, R., C. Behloul, D. Guijarro and M. Yus, 2007. Reductive removal of the Boc protecting group via a DTBB-catalysed lithiation reaction. Arkivoc, 7: 41-50.
  181. Abou, A., F. Foubelo and M. Yus, 2007. Selective lithiation of 1-chloro-n-phenylsulfanylalkanes. Arkivoc, 5: 191-201.
  182. Abou, A., F. Foubelo and M. Yus, 2007. Chemoselective lithiation of 6�chloro�1�halohex�1�ynes with lithium/naphthalene. Tetrahedron, 63: 6625-6634.
  183. Abou, A., F. Foubelo and M. Yus, 2007. 1, n-Bis (phenylsulfanyl) alkanes as precursors of 1, n-dilithio compounds: synthesis of diols. Arkivoc, 4: 196-205.
  184. Ramon, D.J. and M. Yus, 2006. In the arena of enantioselective synthesis, titanium complexes wear the laurel wreath. Chem. Rev., 106: 2126-2208.
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  185. Moglie, Y., F. Alonso, C. Vitale, M. Yus and G. Radivoy, 2006. New active-iron based reducing system for carbonyl compounds and imines. Stereoselective reduction of cyclic ketones. Tetrahedron, 62: 2812-2819.
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  186. Moglie, Y., F. Alonso, C. Vitale, M. Yus and G. Radivoy, 2006. Active-iron-promoted hydrodehalogenation of organic halides. Appl. Catal. A: Gen., 313: 94-100.
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  187. Melero, C., A. Guijarro and M. Yus, 2006. Reactivity in the upper limits of the reduction potential in solution: arene dianion intermolecular carbolithiation of alkenes. Tetrahedron lett., 47: 6267-6271.
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  188. Melendez, J., F. Alonso and M. Yus, 2006. Straightforward synthesis of 1, 6-dioxaspiro [4.4] nonanes. Tetrahedron lett., 47: 1187-1191.
  189. Martinez, R., D.J. Ramon and M. Yus, 2006. RuCl 2 (DMSO) 4 catalyzes the β-alkylation of secondary alcohols with primary alcohols through a hydrogen autotransfer process. Tetrahedron, 62: 8982-8987.
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  190. Martinez, R., D.J. Ramon and M. Yus, 2006. Easy α-alkylation of ketones with alcohols through a hydrogen autotransfer process catalyzed by RuCl 2 (DMSO) 4. Tetrahedron, 62: 8988-9001.
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  191. Goez, C., B. Macia, V.J. Lillo and M. Yus, 2006. [1, 2]-Wittig rearrangement from chloromethyl ethers. Tetrahedron, 62: 9832-9839.
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  192. Forrat, V.J., O. Prieto, D.J. Ramon and M. Yus, 2006. trans-1-Sulfonylamino-2-isoborneolsulfonylaminocyclohexane Derivatives: Excellent chiral ligands for the catalytic enantioselective addition of organozinc reagents to ketones. Chem. A Eur. J., 12: 4431-4445.
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  193. Forrat, V.J., D.J. Ramon and M. Yus, 2006. Polymer supported trans-1-phenylsulfonylamino-2-isoborneolsulfonylaminocyclohexane ligand for the titanium catalyzed organozinc addition to ketones. Tetrahedron: Asymmetry, 17: 2054-2058.
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  194. Behloul, C., D. Guijarro and M. Yus, 2006. Deacylation of esters, thioesters and amides by a naphthalene-catalysed lithiation. Synth., 2006: 309-314.
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  195. Azzena, U., G. Dettori, G. Sforazzini, M. Yus and F. Foubelo, 2006. Regioselectivity in arene-catalyzed reductive lithiation of acetals of chlorobenzaldehydes. Tetrahedron, 62: 1557-1563.
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  196. Alonso, F., J.J. Calvino, S.I. Osante and M. Yus, 2006. Preparation of nickel (0) nanoparticles by arene-catalysed reduction of different nickel chloride-containing systems. J. Exp. Nanosci., 1: 419-433.
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  197. Alonso, F., J. Melendez, T. Soler and M. Yus, 2006. A direct synthesis of 1, 7-dioxaspiro [4.5] decanes from the new 3-methylidenepentane-1, 5-dianion synthon. Tetrahedron, 62: 2264-2277.
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  198. Alonso, F., I. Osante and M. Yus, 2006. Highly stereoselective semihydrogenation of alkynes promoted by nickel (0) nanoparticles. Adv. Synth. Catal., 348: 305-308.
  199. Alonso, F., I. Osante and M. Yus, 2006. Conjugate reduction of α, β-unsaturated carbonyl compounds promoted by nickel nanoparticles. Synlett, 2006: 3017-3020.
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  200. Almansa, R., D. Guijarro and M. Yus, 2006. Nickel-accelerated addition of dialkylzinc reagents to aldehydes. Application to enantioselective synthesis. Arkivoc, 4: 18-28.
  201. Abou, A., F. Foubelo and M. Yus, 2006. Arene-promoted lithiation of 1, n-dihaloalkanes (n= 2�6): a comparative study. Tetrahedron, 62: 10417-10424.
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  202. Yus, M., B. Macia, C. Gomez, T. Soler, L.R. Falvello and P.E. Fanwick, 2005. Reductive ring opening of cis-and trans-2, 3-diphenyloxirane: a common intermediate. Tetrahedron, 61: 3865-3871.
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  203. Yus, M. and D.J. Ramon, 2005. Recent developments in the enantioselective 1, 2-addition of organometallic reagents to carbonyl compounds. Recent Res. Dev. Org. Chem., 6: 297-378.
  204. Yus, M. and D.J. Ramon, 2005. Enantioselective addition of organozinc reagents to carbonyl compounds. Pure appl. Chem., 77: 2111-2119.
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  205. Torregrosa, R., I.M. Pastor and M. Yus, 2005. Isoprene-catalyzed lithiation of imidazole: synthesis of 2-(hydroxyalkyl)-and 2-(aminoalkyl) imidazoles. Tetrahedron, 61: 11148-11155.
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  206. Ramon, D. J. and M. Yus, 2005. Asymmetric multicomponent reactions (AMCRs): the new frontier. Angew. Chem. Int. Ed., 44: 1602-1634.
    CrossRef  |  
  207. Radivoy, G., F. Alonso, Y. Moglie, C. Vitale and M. Yus, 2005. Reduction of alkyl and vinyl sulfonates using the CuCl 2� 2H 2 O�Li�DTBB (cat.) system. Tetrahedron, 61: 3859-3864.
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  208. Pastor, I. M. and M. Yus, 2005. Asymmetric ring opening of epoxides. Curr. Org. Chem., 9: 1-29.
  209. Ortiz, R. and M. Yus, 2005. Tandem intramolecular carbolithiation�transmetallation: from lithium to copper or boron chemistry. Tetrahedron, 61: 1699-1707.
    CrossRef  |  
  210. Martinez, R., G.J. Brand, D.J. Ramon and M. Yus, 2005. [Ru (DMSO) 4] Cl 2 catalyzes the α-alkylation of ketones by alcohols. Tetrahedron lett., 46: 3683-3686.
    CrossRef  |  
  211. Martinez, R., D.J. Ramon and M. Yus, 2005. Catalyst-free multicomponent Strecker reaction in acetonitrile. Tetrahedron lett., 46: 8471-8474.
    CrossRef  |  
  212. Macia, B., C. Gomez and M. Yus, 2005. [2, 3]-Wittig rearrangement by a chlorine�lithium exchange. Tetrahedron lett., 46: 6101-6104.
    CrossRef  |  
  213. Guijarro, D. and M. Yus, 2005. The favorskii rearrangement: synthetic applications. Curr. Org. Chem., 9: 1713-1735.
    Direct Link  |  
  214. Gomez, C., B. Macia, T. Soler and M. Yus, 2005. Bis (chloromethyl) sulfone and sulfoxide as precursors of the corresponding α, α'-dianionic synthons by a chlorine-lithium exchange. Synth., 2005: 3095-3102.
    Direct Link  |  
  215. Gomez, C., B. Macia and M. Yus, 2005. DTBB-catalysed lithiation of 1, 2-bis (phenylsulfanyl) ethene: does 1-lithio-2-phenylsulfanylethene really exist? Tetrahedron, 61: 9325-9330.
    CrossRef  |  
  216. Gomez, C., B. Macia and M. Yus, 2005. DTBB-Catalyzed lithiation of 2, 6-bis (chloromethyl) pyridine. Arkivoc, 9: 10-20.
  217. Foubelo, F., B. Moreno, T. Soler and M. Yus, 2005. Reductive ring opening of dihydrodibenzothiepine and dihydrodinaphtho-oxepine and-thiepine. Tetrahedron, 61: 9082-9096.
    CrossRef  |  
  218. Foubelo, F., A. Abou, and M. Yus, 2005. Chemoselective lithiation of 1-bromo-n-chloroalkanes. Eur. J. org. chem., 2005: 5089-5093.
    CrossRef  |  
  219. Foubelo, F. and M. Yus, 2005. Organodilithium intermediates as useful dianionic synthons: recent advances. Curr. Org. Chem., 9: 459-490.
    CrossRef  |  
  220. Forrat, V.J., D.J. Ramon and M. Yus, 2005. Chiral tertiary alcohols from a trans-1-arenesulfonyl-amino-2-isoborneolsulfonylaminocyclohexane-catalyzed addition of organozincs to ketones. Tetrahedron: Asymmetry, 16: 3341-3344.
    CrossRef  |  
  221. Chinchilla, R., P. Mazon, C. Najera, F.J. Ortega and M. Yus, 2005. Enantioselective michael reactions promoted by recoverable dimeric anthryl-derived cinchona phase-transfer catalysts. Arkivoc, 6: 222-232.
  222. Chinchilla, R., C. Najera and M. Yus, 2005. Functionalized organolithium compounds in total synthesis. Tetrahedron, 61: 3139-3176.
    CrossRef  |  
  223. Behloul, C., D. Guijarro and M. Yus, 2005. Desilylation procedure via a naphthalene-catalysed lithiation reaction. Tetrahedron, 61: 6908-6915.
    CrossRef  |  
  224. Behloul, C., D. Guijarro and M. Yus, 2005. Deallyloxy-and debenzyloxycarbonylation of protected alcohols, amines and thiols via a naphthalene-catalysed lithiation reaction. Tetrahedron, 61: 9319-9324.
    CrossRef  |  
  225. Alonso, F., Y. Moglie, C. Vitale, G. Radivoy and M. Yus, 2005. A new mild deprotecting method for O-benzylsulfonyl phenols and alcohols based on a DTBB-catalyzed lithiation. Synth., 2005: 1971-1976.
    Direct Link  |  
  226. Alonso, F., J.J. Calvino, I. Osante and M. Yus, 2005. A new straightforward and mild preparation of nickel (0) nanoparticles. Chem. Lett., 34: 1262-1263.
  227. Alonso, F., J. Melendez and M. Yus, 2005. A new 3-methylidenepentane-1, 5-dianion synthon: synthesis of perhydropyrano [2, 3-b] pyrans and 1, 7-dioxaspiro [4.5] decanes. Tetrahedron lett., 46: 6519-6524.
    CrossRef  |  
  228. Alonso, F., I.P. Beletskaya and M. Yus, 2005. Non-conventional methodologies for transition-metal catalysed carbon�carbon coupling: a critical overview. Part 1: The heck reaction. Tetrahedron, 61: 11771-11835.
  229. Alonso, F., B. Dacunha, J. Melendez and M. Yus, 2005. Regioselective synthesis of 1, 7-dioxaspiro [4.4] nonanes from a trimethylenemethane dianion synthon. Tetrahedron, 61: 3437-3450.
    CrossRef  |  
  230. Yus, M., R. Torregrosa and I.M. Pastor, 2004. Masked ω-lithio ester enolates: synthetic applications. Mol., 9: 330-348.
  231. Yus, M., B. Moreno and F. Foubelo, 2004. Reductive ring opening of oxygen-containing benzo-fused heterocycles by an arene-catalysed lithiation. Synth., 7: 1115-1118.
  232. Yus, M., and R. Ortiz, 2004. Tandem intramolecular arbolithiation-lithium/zinc transmetallation and applications to carbon− carbon bond‐forming reactions. Eur. J. Org. Chem., 2004: 3833-3841.
  233. Yus, M. and R. Ortiz, 2004. Tandem intramolecular carbolithiation-lithium/zinc transmetallation: a synthetically versatile combination. Lett. Org. Chem., 1: 365-368.
  234. Ramon, D.J. and M. Yus, 2004. Enantioselective synthesis of oxygen-, nitrogen-and halogen-substituted quaternary carbon centers. Curr. Org. Chem., 8: 149-183.
  235. Ramon, D.J. and M. Yus, 2004. Chiral tertiary alcohols made by catalytic enantioselective addition of unreactive zinc reagents to poorly electrophilic ketones? Angew. Chem. Int. Ed., 43: 284-287.
    CrossRef  |  
  236. Guijarro, D., P.J. Martinez, C. Najera and M. Yus, 2004. Benzyllithium from methylated benzylamine and its ammonium salt via naphthalene-catalyzed carbon-nitrogen bond reductive cleavage. Arkivoc, 4: 5-13.
  237. Foubelo, F., B. Moreno and M. Yus, 2004. Reductive opening of 2, 7-dihydrodinaphthoxepine and thiepine: easy regioselective preparation of 2, 2′-difunctionalised binaphthyls. Tetrahedron lett., 45: 8983-8986.
    CrossRef  |  
  238. Foubelo, F., B. Moreno and M. Yus, 2004. Reductive opening of 1H, 3H-benzo [de] isochromene: synthesis of 1, 8-difunctionalised naphthalenes. Tetrahedron, 60: 4655-4662.
    CrossRef  |  
  239. Foubelo, F. and M. Yus, 2004. Indium-mediated diastereoselective addition of allyl bromides to enantiomerically pure N-tert-butylsulfinyl aldimines. Tetrahedron: Asymmetry, 15: 3823-3825.
    CrossRef  |  
  240. Chinchilla, R., C. Najera and M. Yus, 2004. Metalated heterocycles and their applications in synthetic organic chemistry. Chem. Rev., 104: 2667-2722.
    Direct Link  |  
  241. Behloul, C., D. Guijarro and M. Yus, 2004. Detritylation of N-tritylamines via a naphthalene-catalyzed lithiation process. Synth., 8: 1274-1280.
    Direct Link  |  
  242. Alonso, F., Y. Moglie, G. Radivoy, C. Vitale and M. Yus, 2004. Hydrodehalogenation of organic halides using the CuCl 2� 2H 2 O-Li-arene (cat.) combination. Appl. Catal. A: Gen., 271: 171-176.
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  243. Alonso, F., J. Melendez and M. Yus, 2004. Straightforward synthesis of 1, 7-dioxaspiro [4.4] nonanes. Tetrahedron lett., 45: 1717-1720.
    CrossRef  |  
  244. Alonso, F., I.P. Beletskaya and M. Yus, 2004. Transition-metal-catalyzed addition of heteroatom-hydrogen bonds to alkynes. Chem. Rev., 104: 3079-3160.
    Direct Link  |  
  245. Alonso, F. and M. Yus, 2004. The NiCl 2�Li�arene (cat.) combination: A versatile reducing mixture. Chem. Soc. Rev., 33: 284-293.
    Direct Link  |  
  246. Yus, M., R.P. Herrera and A. Guijarro, 2003. Aliphatic organolithiums by fluorine�lithium exchange: n-octyllithium. Tetrahedron lett., 44: 5025-5027.
    CrossRef  |  
  247. Yus, M., R. Ortiz and F.F. Huerta, 2003. Intramolecular carbolithiation promoted by a DTBB-catalysed chlorine�lithium exchange. Tetrahedron, 59: 8525-8542.
    CrossRef  |  
  248. Yus, M., P. Martinez and D. Guijarro, 2003. Direct transformation of allylic and benzylic thiols, thioethers, and disulfides into organolithium compounds. Synth. Commun., 33: 2365-2376.
    Direct Link  |  
  249. Yus, M., D.J. Ramon and O. Prieto, 2003. Synthesis of new C 2-symmetrical bis (hydroxycamphorsulfonamide) ligands and their application in the enantioselective addition of dialkylzinc reagents to aldehydes and ketones. Tetrahedron: Asymmetry, 14: 1103-1114.
    CrossRef  |  
  250. Yus, M., D.J. Ramon and O. Prieto, 2003. (−)‐Frontalin: Synthesis using the catalytic enantioselective addition of dimethylzinc to a ketone. Eur. J. Org. Chem., 2003: 2745-2748.
    Direct Link  |  
  251. Yus, M., D.J. Ramon and I. Gomez, 2003. Preparation of α, n-dilithiotoluene equivalents. Synthesis of tamoxifen. Tetrahedron, 59: 3219-3225.
    CrossRef  |  
  252. Yus, M., C. Najera and F. Foubelo, 2003. The role of 1, 3-dithianes in natural product synthesis. Tetrahedron, 59: 6147-6212.
    CrossRef  |  
  253. Yus, M., C. Gomez and P. Candela, 2003. Functionalised linear and cross-linked polystyrenes from chloromethylated polymers through their organolithium derivatives. Tetrahedron, 59: 1909-1916.
  254. Yus, M., B. Macia and C. Gomez, 2003. 1, 3-Dichloro-2-butene: a useful precursor for the 2-butene-1, 3-dianion and its corresponding 1, 3-dipolar synthon. Tetrahedron, 59: 5183-5192.
    CrossRef  |  
  255. Yus, M., 2003. Ring opening of heterocycles by an arene-catalyzed lithiation. Pure Appl. Chem., 75: 1453-1475.
  256. Yus, M. and J. Gomis, 2003. ZnBr2/CuCN-Promoted, highly regioselective SN2′ reactions of some functionalised organolithium compounds with allylic and propargylic halides. Eur. J. Org. Chem., 2003: 2043-2048.
    CrossRef  |  
  257. Yus, M. and J. Gomis, 2003. Chemoselective acylation of some oxidofunctionalised organolithium compounds. Tetrahedron, 59: 4967-4971.
    CrossRef  |  
  258. Prieto, O., D.J. Ramon and M. Yus, 2003. Highly enantioselective arylation of ketones. Tetrahedron: Asymmetry, 14: 1955-1957.
    CrossRef  |  
  259. Najera, C., J.M. Sansano and M. Yus, 2003. Recent synthetic uses of functionalised aromatic and heteroaromatic organolithium reagents prepared by non-deprotonating methods. Tetrahedron, 59: 9255-9303.
    CrossRef  |  
  260. Najera, C. and M. Yus, 2003. Functionalized organolithium compounds: New synthetic adventures. Curr. Org. Chem., 7: 867-926.
    Direct Link  |  
  261. Herrera, R.P., A. Guijarro and M. Yus, 2003. Primary alkyl fluorides as regioselective alkylating reagents of lithium arene dianions. Easy prediction of regioselectivity by MO calculations on the dianion. Tetrahedron lett., 44: 1313-1316.
    CrossRef  |  
  262. Guijarro, D., P. Martıinez and M. Yus, 2003. Reductive defluorination of fluoroalkanes. Tetrahedron, 59: 1237-1244.
  263. Chinchilla, R., D.J. Dodsworth, C. Najera, J.M. Soriano and M. Yus, 2003. Uronium salts from polymeric N-hydroxysuccinimide (P-HOSu) as new solid-supported peptide coupling reagents. Arkivoc, 10: 41-47.
  264. Alonso, F., P. Candela, C. Gomez and M. Yus, 2003. The NiCl2-Li-Arene (cat.) combination as reducing system, part 9: catalytic hydrogenation of organic compounds using the NiCl2-Li-(Naphthalene or Polymer-Supported Naphthalene)(cat.) combination. Adv. Synth. Catal., 345: 275-279.
    Direct Link  |  
  265. Alonso, F., J. Melendez and M. Yus, 2003. Dilithiated synthons: synthesis of cyclic ethers. Russ. Chem. Bull., 52: 2628-2635.
    Direct Link  |  
  266. Alonso, F., G. Radivoy and M. Yus, 2003. Active nickel-based reduction of organic compounds. Russ. Chem. Bull., 52: 2563-2576.
    Direct Link  |  
  267. Alonso, F., E. Lorenzo, J. Melendez and M. Yus, 2003. Straight and versatile synthesis of substituted perhydrofuro [2, 3-b] pyrans from 2-chloromethyl-3-(2-methoxyethoxy) propene. Tetrahedron, 59: 5199-5208.
    CrossRef  |  
  268. Yus, M., T. Soler and F. Foubelo, 2002. Reaction of functionalized organolithium compounds with substituted oxiranes: useful methodology for 1, 6-and 1, 7-diols, and tetrahydrobenzoxepines. Tetrahedron, 58: 7009-7016.
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  269. Yus, M., R.P. Herrera and A. Guijarro, 2002. On the mechanism of arene-catalyzed lithiation: The role of arene dianions-naphthalene radical anion versus naphthalene dianion. Chem. A Eur. J., 8: 2574-2584.
    CrossRef  |  
  270. Yus, M., R. Ortiz and F.F. Huerta, 2002. DTBB-catalysed lithiation of 6-chloro-1-hexene and related systems: synthetically useful temperature-dependent behaviour. Tetrahedron Lett., 43: 2957-2960.
    CrossRef  |  
  271. Yus, M., J. Ortiz and C. Najera, 2002. α-Lithioenamines by chlorine-lithium exchange: Versatile acyl anion equivalents. Arkivoc, 5: 38-47.
  272. Yus, M., F. Foubelo, J.V. Ferrandez and A. Bachki, 2002. Reductive lithiation of cyclic benzofused ethers: a source of oxygen-functionalised organolithium compounds. Tetrahedron, 58: 4907-4915.
    CrossRef  |  
  273. Yus, M., F. Foubelo and J.V. Ferrandez, 2002. Thianthrene as a source of the 1, 2-benzene dianion. Tetrahedron lett., 43: 7205-7207.
    CrossRef  |  
  274. Yus, M., F. Foubelo and J.V. Ferrandez, 2002. DTBB-Catalyzed lithiation of 4-hetero-substituted dibenzothiins. Chem. Lett., 7: 726-727.
  275. Yus, M., D.J. Ramon and O. Prieto, 2002. Synthesis of C 2-symmetrical bis (1, 2-hydroxy sulfonamide) ligands and application in the enantioselective addition of dialkylzinc to aldehydes. Tetrahedron: Asymmetry, 13: 1573-1579.
    CrossRef  |  
  276. Yus, M., D.J. Ramon and O. Prieto, 2002. Highly enantioselective addition of dialkylzinc reagents to ketones promoted by titanium tetraisopropoxide. Tetrahedron: Asymmetry, 13: 2291-2293.
    CrossRef  |  
  277. Yus, M., D.J. Ramon and I. Gomez, 2002. Six-and five-membered 3-alkoxy-2-lithiocycloalkenes: new stable non-anionic β-functionalised organolithium compounds. Tetrahedron, 58: 5163-5172.
  278. Yus, M., D.J. Ramon and I. Gomez, 2002. Lithiophenylalkyllithiums: new dilithium reagents having both sp 2-and sp 3-hybridised remote carbanionic centres. J. Organomet. Chem., 663: 21-31.
    CrossRef  |  
  279. Yus, M., C. Gomez and P. Candela, 2002. Polyphenylene as an electron transfer catalyst in lithiation processes. Tetrahedron, 58: 6207-6210.
    CrossRef  |  
  280. Yus, M. and J. Gomis, 2002. Palladium-promoted arylation of functionalised organolithium compounds via their zinc derivatives. Eur. J. Org. Chem., 2002: 1989-1995.
    CrossRef  |  
  281. Yus, M. and F. Foubelo, 2002. Reductive opening of heterocycles with lithium metal as a source of functionalized organolithium compounds: synthetic applications. Targets Heterocycl. Syst., 6: 136-171.
  282. Yus, M. and F. Foubelo, 2002. Enedynes : Recent developments. Recent Res. Dev. Org. Chem., 6: 205-280.
  283. Yus, M. and D.J. Ramon, 2002. From lithium to other metals. Our penultimate immersion into the arene-catalyzed reaction ocean. Latv. J. Chem., .
  284. Alonso, F., J. Melendez and M. Yus, 2002. Synthesis of substituted 1, 5-dioxaspiro [2.4] heptanes from 2, 3-dichloroprop-1-ene. Helv. Chim. Acta, 85: 3262-3271.
    CrossRef  |  
  285. Alonso, F., I.P. Beletskaya and M. Yus, 2002. Metal-mediated reductive hydrodehalogenation of organic halides. Chem. Rev., 102: 4009-4092.
    Direct Link  |  
  286. Yus, M., T. Soler and F. Foubelo, 2001. A new and direct synthesis of 2-substituted pyrrolidines. J. Org. Chem., 66: 6207-6208.
    CrossRef  |  PubMed  |  Direct Link  |  
  287. Yus, M., S. Ma, L. Li, F. Scheufler and M.E. Maier et al., 2001. From arene-catalyzed lithiation to other synthetic adventures. Synlett, 2001: 1197-1205.
  288. Yus, M., R.P. Herrera and A. Guijarro, 2001. On the mechanism of the naphthalene-catalysed lithiation: The role of the naphthalene dianion. Tetrahedron Lett., 42: 3455-3458.
    CrossRef  |  Direct Link  |  
  289. Yus, M., P. Martinez and D. Guijarro, 2001. DTBB-catalysed dilithiation of styrene and its methyl-derivatives: Introduction of two electrophilic reagents. Tetrahedron, 57: 10119-10124.
    CrossRef  |  Direct Link  |  
  290. Yus, M., I.M. Pastor and J. Gomis, 2001. Lewis acid-promoted conjugate addition of functionalised organolithium compounds to electrophilic olefins. Tetrahedron, 57: 5799-5805.
    CrossRef  |  Direct Link  |  
  291. Yus, M., G. Radivoy and F. Alonso, 2001. Lithium/DTBB-induced reduction of N-alkoxyamides and acyl azides. Synthesis, 2001: 914-918.
  292. Yus, M., F. Foubelo and J.V. Ferrandez, 2001. Stereoselective reductive opening of 2, 3-benzofuran- A two-step synthesis of 2H-chromenes including deoxycordiachromene. Eur. J. Org. Chem., 2001: 2809-2813.
    CrossRef  |  Direct Link  |  
  293. Yus, M., C. Gomez and P. Candela, 2001. The first direct formation of an organolithium reagent on a soluble polymer by chlorine-lithium exchange: Functionalised linear polystyrene. Tetrahedron Lett., 42: 3977-3979.
    CrossRef  |  Direct Link  |  
  294. Yus, M., A. Gutierrez and F. Foubelo, 2001. Polylithiation of thioethers: A versatile route for polyanionic synthons. Tetrahedron, 57: 4411-4422.
    CrossRef  |  Direct Link  |  
  295. Yus, M. and J. Gomis, 2001. Negishi cross-coupling with functionalised organozinc compounds prepared by lithium-zinc transmetallation. Tetrahedron Lett., 42: 5721-5724.
    CrossRef  |  Direct Link  |  
  296. Yus, M. and F. Foubelo, 2001. DTBB-catalysed lithiation of 1, 7-dihydrodibenzothiepin. Tetrahedron Lett., 42: 2469-2472.
    CrossRef  |  Direct Link  |  
  297. Radivoy, G., F. Alonso and M. Yus, 2001. Two new methodologies for the deoxygenation and reduction of nitrones based on the use of lithium and DTBB (cat.). Synthesis, 2001: 427-430.
  298. Pastor, I.M. and M. Yus, 2001. New reactivity of functionalised organolithium compounds in the presence of Cu (I) or Cu (II) salts: Conjugate addition, acylation or dimerisation. Tetrahedron, 57: 2371-2378.
    CrossRef  |  Direct Link  |  
  299. Pastor, I.M. and M. Yus, 2001. Masked β-,γ-and δ-lithium ester enolates: Useful reagents in organic synthesis. Tetrahedron Lett., 42: 1029-1032.
  300. Pastor, I.M. and M. Yus, 2001. Functionalised organotitanium compounds: From lithium to titanium intermediates in chemoselective reactions with carbonyl compounds. Tetrahedron, 57: 2365-2370.
    CrossRef  |  Direct Link  |  
  301. Guijarro, D. and M. Yus, 2001. Pinacol-type coupling reactions: Recente developments. Res. Adv. Org. Chem., 2001: 1-22.
  302. Guijarro, D. and M. Yus, 2001. Generation of allylic and benzylic organolithium compounds by fluorine-lithium exchange: Reaction with electrophiles. J. Organomet. Chem., 624: 53-57.
    CrossRef  |  Direct Link  |  
  303. Foubelo, F., T. Soler and M. Yus, 2001. EPC-Synthesis of functionalised steroids from estrone and cholestanone through organolithium intermediates. Tetrahedron: Asymmetry, 12: 801-810.
  304. Alonso, F. and M. Yus, 2001. The hydrogenation of cyclododecene by lithium naphthalenide and nickel chloride dihydrate. J. Chem. Educ., 78: 1517-1518.
    CrossRef  |  Direct Link  |  
  305. Alonso, F. and M. Yus, 2001. The NiCl2-Li-Arene (cat.) combination as reducing system: Part 8: Catalytic hydrogenation of organic compounds using the NiCl2-Li-naphtalene (cat.) combination. Adv. Synth. Catal., 343: 188-191.
  306. Soler, T., A. Bachki, L.R. Falvello, F. Foubelo and M. Yus, 2000. Structural modification of carbohydrates via functionalised organolithium intermediates: EPC preparation of branched-chain functionalised sugars. Tetrahedron: Asymmetry, 11: 493-517.
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  307. Ramon, D.J. and M. Yus, 2000. New methodologies based on arene-catalyzed lithiation reactions and their application to synthetic organic chemistry. Eur. J. Org. Chem., 2000: 225-237.
    CrossRef  |  Direct Link  |  
  308. Prieto, O., D.J. Ramon and M. Yus, 2000. Camphordisulfonamides: Good chiral ligands for the addition of dialkylzinc to aliphatic aldehydes. Tetrahedron: Asymmetry, 11: 1629-1644.
    CrossRef  |  Direct Link  |  
  309. Pastor, I.M. and M. Yus, 2000. Lithium-α-lithioacetate and β-lithiopropionate: Useful intermediates in organic synthesis. Tetrahedron Lett., 41: 5335-5339.
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  310. Pastor, I.M. and M. Yus, 2000. Copper (I) or (II)-mediated conjugate addition or dimerisation of functionalised organolithium compounds. Tetrahedron Lett., 41: 1589-1592.
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  311. Lorenzo, E., F. Alonso and M. Yus, 2000. Substituted perhydrofuropyrans: Easy preparation from 2-chloromethyl-3-(2-methoxyethoxy) propene through 3-methylene-1, 6-diols. Tetrahedron Lett., 41: 1661-1665.
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  312. Lorenzo, E., F. Alonso and M. Yus, 2000. New trimethylenemethane dianion synthons: Application to the preparation of substituted perhydrofuro [2, 3-b] furans. Tetrahedron, 56: 1745-1757.
    CrossRef  |  Direct Link  |  
  313. Guijarro, D. and M. Yus, 2000. Arene-catalysed lithiation of fluoroarenes. Tetrahedron, 56: 1135-1138.
    CrossRef  |  Direct Link  |  
  314. Guijarro, A., C. Gomez and M. Yus, 2000. Active metals in organic synthesis: Recent advances. Trends Org. Chem., 8: 65-91.
  315. Gomez, I., E. Alonso, D.J. Ramon and M. Yus, 2000. Naphthalene-catalysed lithiation of chlorinated nitrogenated aromatic heterocycles and reaction with electrophiles. Tetrahedron, 56: 4043-4052.
    CrossRef  |  Direct Link  |  
  316. Foubelo, F., S.A. Saleh and M. Yus, 2000. 3-Chloropropyl and 4-chlorobutyl phenyl ethers as sources of 1, 3-dilithiopropane and 1, 4-dilithiobutane: sequential reaction with carbonyl compounds. J. Org. Chem., 65: 3478-3483.
    CrossRef  |  PubMed  |  Direct Link  |  
  317. Foubelo, F., C. Gomez, A. Gutierrez and M. Yus, 2000. Synthesis of substituted tetrahydroisoquinolines and benzo[d]azepines from phtalan or isochroman and N-silaldimines. J. Heterocycl. Chem., 37: 1061-1064.
  318. Foubelo, F. and M. Yus, 2000. 1, 3-Bis (phenylmercapto) propane and 1-chloro-3-(phenylmercapto) propane: Useful precursors for 1, 3-dilithiopropane synthons in the preparation of 1, 5-diols. Tetrahedron Lett., 41: 5047-5051.
    CrossRef  |  Direct Link  |  
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