Dr. Viktor V. Zhdankin

Professor
Department of Chemistry, University of Minnesota, Duluth, USA

Highest Degree
Ph.D. in Chemical Sciences from Moscow State University, Russia

My URL
https://livedna.org/712.23822

Share this Profile

Area of Interest:

Chemistry
Sustainable Chemistry
Organic Chemistry
Catalysis Chemistry
Heterocycles

Selected Publications

  1. Zhdankin, V., 2022. Introduction to hypervalent iodine chemistry. Arkivoc, 2022: 1-6.
    CrossRef  |  Direct Link  |  

  2. Umakoshi, Y., Y. Takemoto, A. Tsubouchi, V.V. Zhdankin, A. Yoshimura and A. Saito, 2022. Dehydrogenative cycloisomerization/arylation sequence of N-propargyl carboxamides with arenes by iodine(III)-catalysis. Adv. Synth. Catal., 364: 2053-2059.
    CrossRef  |  Direct Link  |  

  3. Soni, S., Rimi, V. Kumar, K. Kikushima, T. Dohi, V.V. Zhdankin and R. Kumar, 2022. Hypervalent iodine (V) catalyzed reactions. Arkivoc, 2022: 27-56.
    CrossRef  |  Direct Link  |  

  4. Soldatova, N.S., P.S. Postnikov, D.M. Ivanov, O.V. Semyonov and O.S. Kukurina et al., 2022. Zwitterionic iodonium species afford halogen bond-based porous organic frameworks. Chem. Sci., 13: 5650-5658.
    CrossRef  |  Direct Link  |  

  5. Rimi, S. Soni, B. Uttam, H. China, T. Dohi , V.V. Zhdankin and R. Kumar, 2022. Recyclable hypervalent iodine reagents in modern organic synthesis. Synthesis, 54: 2731-2748.
    CrossRef  |  Direct Link  |  

  6. Ozerskaya, A.V., M.S. Larkina, E.V. Podrezova, D.Y. Svitich, R.Y. Yusubova, V.V. Zhdankin and M.S. Yusubov, 2022. Synthesis of 2-fluorobenzoic acids by nucleophilic fluorination of 1-arylbenziodoxolones. ARKIVOC, 2022: 108-125.
    CrossRef  |  Direct Link  |  

  7. Mironova, I.A., S.F. Kirsch, V.V. Zhdankin, A. Yoshimura and M.S. Yusubov, 2022. Hypervalent iodine-mediated azidation reactions. Eur. J. Org. Chem., Vol. 2022. 10.1002/ejoc.202200754.
    CrossRef  |  Direct Link  |  

  8. Yusubov, M.S. and V.V. Zhdankin, 2021. Zefirov's reagent and related hypervalent iodine triflates. Mendeleev Commun., 31: 282-287.
    CrossRef  |  Direct Link  |  

  9. Yoshimura, A., C.D. Huss, M. Liebl, G.T. Rohde and S.M. Larson et al., 2021. Preparation, structure, and reactivity of pseudocyclic β‐trifluorosulfonyloxy vinylbenziodoxolone derivatives. Adv. Synth. Catal., 363: 3365-3371.
    CrossRef  |  Direct Link  |  

  10. Yoshimura, A., C.D. Huss, A. Saito, T. Kitamura and V.V. Zhdankin, 2021. 2-Iodosylbenzoic acid activated by trifluoromethanesulfonic anhydride: Efficient oxidant and electrophilic reagent for preparation of iodonium salts. New J. Chem., 45: 16434-16437.
    CrossRef  |  Direct Link  |  

  11. Sviridova, E., M. Li, A. Barras, A. Addad and M.S. Yusubov et al., 2021. Aryne cycloaddition reaction as a facile and mild modification method for design of electrode materials for high-performance symmetric supercapacitor. Electrochim. Acta, Vol. 369. 10.1016/j.electacta.2020.137667.
    CrossRef  |  Direct Link  |  

  12. Shea, M.T., G.T. Rohde, Y.A. Vlasenko, P.S. Postnikov and M.S. Yusubov et al., 2021. Convenient synthesis of benziodazolone: New reagents for direct esterification of alcohols and amidation of amines. Molecules, Vol. 26. 10.3390/molecules26237355.
    CrossRef  |  Direct Link  |  

  13. Antonkin, N.S., Y.A. Vlasenko, A. Yoshimura, V.I. Smirnov and T.N. Borodina et al., 2021. Preparation and synthetic applicability of imidazole-containing cyclic iodonium salts. J. Org. Chem., 86: 7163-7178.
    CrossRef  |  Direct Link  |  

  14. Zhdankin, V.V., M.S. Yusubov, P. Postnikov and A. Yoshimura, 2020. Benziodoxole-derived organosulfonates: The strongest hypervalent iodine electrophiles and oxidants. Synlett 31: 315-326.
    CrossRef  |  Direct Link  |  

  15. Zhdankin, V.V., 2020. Hypervalent iodine compounds: Reagents of the future. Arkivoc, 2020: 1-11.
    CrossRef  |  Direct Link  |  

  16. Yoshimura, A., A. Saito, V.V. Zhdankin and M.S. Yusubov, 2020. Synthesis of oxazoline and oxazole derivatives by hypervalent-iodine-mediated oxidative cycloaddition reactions. Synthesis, 52: 2299-2310.
    CrossRef  |  Direct Link  |  

  17. Takahashi, S., Y. Umakoshi, K. Nakayama, Y. Okada, V.V. Zhdankin, A. Yoshimura and A. Saito, 2020. Fluorocyclization of N-propargyl carboxamides by λ3-iodane catalysts with coordinating substituents. Adv. Synth. Catal., 362: 2997-3003.
    CrossRef  |  Direct Link  |  

  18. Makitalo, C.L., A. Yoshimura, G.T. Rohde, I.A. Mironova and R.Y. Yusubova et al., 2020. Imino-λ3-iodane and catalytic amount of I2-mediated synthesis of N-allylsulfenamides via [2,3]-sigmatropic rearrangement. Eur. J. Org. Chem., 2020: 6433-6439.
    CrossRef  |  Direct Link  |  

  19. Yusubov, M.S., N.S. Soldatova, P.S. Postnikov, R.R. Valiev and D.Y. Svitich et al., 2018. Reactions of 1‐arylbenziodoxolones with Azide anion: Experimental and computational study of substituent effects. Eur. J. Organic Chem., 2018: 640-647.
    CrossRef  |  Direct Link  |  

  20. Shimizu, H., A. Yoshimura, K. Noguchi, V.N. Nemykin, V.V. Zhdankin and A. Saito, 2018. Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine (III) reagents. Beilstein J. Organic Chem., 14: 531-536.
    CrossRef  |  

  21. Zhdankin, V.V. and K. Muniz, 2017. Editorial for the special issue on hypervalent iodine reagents. J. Org. Chem., 82: 11667-11668.
    Direct Link  |  

  22. Zhdankin, V.V. and A.N. Pestryakov, 2017. Special issue on organic synthesis and hydrocarbon feedstock refining. Curr. Organic Synthesis, 14: 322-322.
    Direct Link  |  

  23. Yusubov, M., P. Postnikov, R. Yusubova, A. Yoshimura, G. Jurjens, A. Kirschning and V. Zhdankin, 2017. 2‐iodoxybenzoic acid tosylates: The alternative to dess‐martin Periodinane Oxidizing reagents. Adv. Synthesis Catalysis, 359: 3207-3216.
    CrossRef  |  Direct Link  |  

  24. Yoshimura, A., S.C. Klasen, M.T. Shea, K.C. Nguyen and G.T. Rohde et al., 2017. Preparation, structure and reactivity of pseudocyclic benziodoxole tosylates: New hypervalent iodine oxidants and electrophiles. Chem. Eur. J., 23: 691-695.
    CrossRef  |  Direct Link  |  

  25. Yoshimura, A., K.C. Nguyen, G.T. Rohde, P.S. Postnikov, M.S. Yusubov and V.V. Zhdankin, 2017. Hypervalent iodine reagent mediated oxidative heterocyclization of aldoximes with heterocyclic alkenes. J. Organic Chem., 82: 11742-11751.
    CrossRef  |  Direct Link  |  

  26. Yoshimura, A., J.M. Fuchs, K.R. Middleton, A.V. Maskaev and G.T. Rohde et al., 2017. Pseudocyclic arylbenziodoxaboroles: Efficient benzyne precursors triggered by water at room temperature. Chem. Eur. J., 23: 16738-16742.
    CrossRef  |  Direct Link  |  

  27. Yagyu, T., Y. Takemoto, A. Yoshimura, V.V. Zhdankin and A. Saito, 2017. Iodine (III)-catalyzed formal [2+ 2+ 1] cycloaddition reaction for metal-free construction of Oxazoles. Organic Lett., 19: 2506-2509.
    CrossRef  |  Direct Link  |  

  28. Soldatova, N., P. Postnikov, O. Kukurina, V.V. Zhdankin, A. Yoshimura, T. Wirth and M.S. Yusubov, 2017. Facile one‐pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone. ChemistryOpen, 6: 18-20.
    CrossRef  |  Direct Link  |  

  29. Okamura, Y., D. Sato, A. Yoshimura, V. Zhdankin and A. Saito, 2017. Iodine (III)‐mediated/catalyzed cycloisomerization-amination sequence of N‐propargyl carboxamides. Adv. Synthesis Catalysis, 359: 3243-3247.
    CrossRef  |  Direct Link  |  

  30. Morozova, M.A., M.S. Yusubov, B. Kratochvil, V. Eigner and A.A. Bondarev et al., 2017. Regioselective Zn (OAc) 2-catalyzed azide-alkyne cycloaddition in water: The green click-chemistry. Organic Chem. Frontiers, 4: 978-985.
    Direct Link  |  

  31. Baba, T., S. Takahashi, Y. Kambara, A. Yoshimura, V.N. Nemykin, V.V. Zhdankin and A. Saito, 2017. Development of imino‐λ3‐iodanes with improved reactivity for metal‐free [2+ 2+ 1] cycloaddition‐type reactions. Adv. Synthesis Catalysis, 359: 3860-3864.
    CrossRef  |  Direct Link  |  

  32. Zhdankin, V.V., 2016. Hypervalent heterocycles. Adv. Heterocyclic Chem., 119: 57-79.

  33. Yoshimura, A., M.S. Yusubov and V.V. Zhdankin, 2016. Synthetic applications of pseudocyclic hypervalent iodine compounds. Organic Biomolecular Chem., 14: 4771-4781.
    CrossRef  |  Direct Link  |  

  34. Yoshimura, A., K.C. Nguyen, S.C. Klasen, P.S. Postnikov and M.S. Yusubov et al., 2016. Hypervalent iodine‐catalyzed synthesis of 1, 2, 4‐oxadiazoles from aldoximes and nitriles. Asian J. Organic Chem., 5: 1128-1133.
    CrossRef  |  Direct Link  |  

  35. Yoshimura, A., K.C. Nguyen, G.T. Rohde, A. Saito, M.S. Yusubov and V.V. Zhdankin, 2016. Oxidative cycloaddition of aldoximes with maleimides using catalytic hydroxy (aryl) iodonium species. Adv. Synthesis Catalysis, 358: 2340-2344.
    CrossRef  |  Direct Link  |  

  36. Yoshimura, A. and V.V. Zhdankin, 2016. Advances in synthetic applications of hypervalent iodine compounds. Chem. Rev., 116: 3328-3435.
    CrossRef  |  Direct Link  |  

  37. Soldatova, N., P. Postnikov, A.A. Troyan, A. Yoshimura, M.S. Yusubov and V.V. Zhdankin, 2016. Mild and efficient synthesis of iodylarenes using Oxone as oxidant. Tetrahedron Lett., 57: 4254-4256.
    CrossRef  |  Direct Link  |  

  38. Petunin, P.V., R.R. Valiev, R.G. Kalinin, M.E. Trusova, V.V. Zhdankin and P.S. Postnikov, 2016. General and simple method for the synthesis of 3-nitroformazan using arenediazonium tosylates. Curr. Organic Synthesis, 13: 623-628.
    Direct Link  |  

  39. Mironova, I.A., R.Y. Yusubova, O.S. Kukurina, M.S. Yusubov and V.V. Zhdankin, 2016. Potassium 4-iodylbenzenesulfonate (PIBS): An efficient recyclable hypervalent iodine reagent for iodo-functionalization of alkenes, alkynes and ketones. Curr. Organic Synthesis, 13: 629-637.
    Direct Link  |  

  40. Asari, N., Y. Takemoto, Y. Shinomoto, T. Yagyu, A. Yoshimura, V.V. Zhdankin and A. Saito, 2016. Catalytic cycloisomerization–fluorination sequence of N‐propargyl amides by iodoarene/HF⋅ Pyridine/selectfluor systems. Asian J. Organic Chem., 5: 1314-1317.
    CrossRef  |  Direct Link  |  

  41. Zhdankin, V.V., 2015. Iodine heterocycles. Adv. Heterocyclic Chem., 115: 1-91.

  42. Yusubov, M.S., D.Y. Svitich, A. Yoshimura, B.J. Kastern, V.N. Nemykin and V.V. Zhdankin, 2015. Preparation, X‐ray structure and reactivity of triisopropylsilyl‐substituted aryliodonium salts. Eur. J. Organic Chem., 2015: 4831-4834.
    CrossRef  |  Direct Link  |  

  43. Yusubov, M.S. and V.V. Zhdankin, 2015. Iodine catalysis: A green alternative to transition metals in organic chemistry and technology. Resour. Efficient Technol., 1: 49-67.
    CrossRef  |  Direct Link  |  

  44. Yoshimura, A., S.R. Koski, J.M. Fuchs, A. Saito, V.N. Nemykin and V.V. Zhdankin, 2015. Saccharin‐based μ‐Oxo imidoiodane: A readily available and highly reactive reagent for electrophilic amination. Chem. Eur. J., 21: 5328-5331.
    CrossRef  |  Direct Link  |  

  45. Yoshimura, A., K.C. Nguyen, S.C. Klasen, A. Saito, V.N. Nemykin and V.V. Zhdankin, 2015. Preparation, structure and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent. Chem. Commun., 51: 7835-7838.
    CrossRef  |  Direct Link  |  

  46. Shinomoto, Y., A. Yoshimura, H. Shimizu, M. Yamazaki, V.V. Zhdankin and A. Saito, 2015. Tetra-n-butylammonium iodide catalyzed C-H azidation of aldehydes with thermally stable azidobenziodoxolone. Organic Lett., 17: 5212-5215.
    CrossRef  |  Direct Link  |  

  47. Saito, A., Y. Kambara, T. Yagyu, K. Noguchi, A. Yoshimura and V.V. Zhdankin, 2015. Metal‐free [2+ 2+ 1] annulation of alkynes, nitriles and nitrogen atoms from iminoiodanes for synthesis of highly substituted imidazoles. Adv. Synthesis Catalysis, 357: 667-671.
    CrossRef  |  Direct Link  |  

  48. Postnikov, P.S., O.A. Guselnikova, M.S. Yusubov, A. Yoshimura, V.N. Nemykin and V.V. Zhdankin, 2015. Preparation and X-ray structural study of dibenziodolium derivatives. J. Organic Chem., 80: 5783-5788.
    CrossRef  |  Direct Link  |  

  49. Zhdankin, V.V. and J.D. Protasiewicz, 2014. Development of new hypervalent iodine reagents with improved properties and reactivity by redirecting secondary bonds at iodine center. Coordination Chem. Rev., 275: 54-62.
    CrossRef  |  Direct Link  |  

  50. Yusubov, M.S., C. Celik, M.R. Geraskina, A. Yoshimura, V.V. Zhdankin and V.N. Nemykin, 2014. Binuclear iron (III) octakis (perfluorophenyl) tetraazaporphyrin μ-oxodimer: A highly efficient catalyst for biomimetic oxygenation reactions. Tetrahedron Lett., 55: 5687-5690.
    CrossRef  |  Direct Link  |  

  51. Yoshimura, A., T.N. Jones, M.S. Yusubov and V.V. Zhdankin, 2014. Hypoiodite‐mediated catalytic cyclopropanation of alkenes with malononitrile. Adv. Synthesis Catalysis, 356: 3336-3340.
    CrossRef  |  Direct Link  |  

  52. Yoshimura, A., S.R. Koski, B.J. Kastern, J.M. Fuchs and T.N. Jones et al., 2014. Hypoiodite‐mediated cyclopropanation of alkenes. Chem. Eur. J., 20: 5895-5898.
    CrossRef  |  Direct Link  |  

  53. Yoshimura, A., A.D. Todora, B.J. Kastern, S.R. Koski and V.V. Zhdankin, 2014. Synthesis of 1, 2, 4‐thiadiazoles by oxidative dimerization of carbothioamides by using Oxone. Eur. J. Organic Chem., 2014: 5149-5152.
    CrossRef  |  Direct Link  |  

  54. Ivanov, A.S., I.A. Popov, A.I. Boldyrev and V.V. Zhdankin, 2014. The I= X (X= O, N, C) double bond in hypervalent iodine compounds: Is it real? Angewandte Chem., 126: 9771-9775.
    CrossRef  |  Direct Link  |  

  55. Zhdankin, V.V., 2013. Hypervalent Iodine Chemistry: Preparation, Structure and Synthetic Applications of Polyvalent Iodine Compounds. John Wiley and Sons, Chichester, ISBN: 9781118341308, Pages: 480.

  56. Yusubov, M.S., Svitich, D. Yu, M.S. Larkina and V.V. Zhdankin, 2013. Applications of iodonium salts and iodonium ylides as precursors for nucleophilic fluorination in positron emission tomography. ARKIVOC, 1: 364-395.

  57. Yusubov, M.S., R.Y. Yusubova, V.N. Nemykin and V.V. Zhdankin, 2013. Preparation and X-ray structural study of 1-arylbenziodoxolones. J. Organic Chem., 78: 3767-3773.
    CrossRef  |  Direct Link  |  

  58. Yusubov, M.S., D.Y. Svitich, A. Yoshimura, V.N. Nemykin and V.V. Zhdankin, 2013. 2-Iodoxybenzoic acid organosulfonates: Preparation, X-ray structure and reactivity of new, powerful hypervalent iodine (v) oxidants. Chem. Commun., 49: 11269-11271.
    CrossRef  |  Direct Link  |  

  59. Yoshimura, A., K.R. Middleton, A.D. Todora, B.J. Kastern, S.R. Koski, A.V. Maskaev and V.V. Zhdankin, 2013. Hypervalent iodine catalyzed generation of nitrile oxides from oximes and their cycloaddition with alkenes or alkynes. Organic Lett., 15: 4010-4013.
    CrossRef  |  Direct Link  |  

  60. Yoshimura, A., C. Zhu, K.R. Middleton, A.D. Todora, B.J. Kastern, A.V. Maskaev and V.V. Zhdankin, 2013. Hypoiodite mediated synthesis of isoxazolines from aldoximes and alkenes using catalytic KI and Oxone as the terminal oxidant. Chem. Commun., 49: 4800-4802.
    CrossRef  |  Direct Link  |  

  61. Zhu, C., A. Yoshimura, Y. Wei, V.N. Nemykin and V.V. Zhdankin, 2012. Facile preparation and reactivity of bifunctional ionic liquid-supported hypervalent iodine reagent: A convenient recyclable reagent for catalytic oxidation. Tetrahedron Lett., 53: 1438-1444.
    CrossRef  |  Direct Link  |  

  62. Zhu, C., A. Yoshimura, P. Solntsev, L. Ji, Y. Wei, V.N. Nemykin and V.V. Zhdankin, 2012. New highly soluble dimedone-derived iodonium ylides: Preparation, X-ray structure and reaction with carbodiimide leading to oxazole derivatives. Chem. Commun., 48: 10108-10110.
    CrossRef  |  Direct Link  |  

  63. Zhu, C., A. Yoshimura, L. Ji, Y. Wei, V.N. Nemykin and V.V. Zhdankin, 2012. Design, preparation, X-ray crystal structure and reactivity of o-Alkoxyphenyliodonium Bis (methoxycarbonyl) methanide, a highly soluble Carbene precursor. Organic Lett., 14: 3170-3173.
    CrossRef  |  Direct Link  |  

  64. Yusubov, M.S., R.Y. Yusubova, V.N. Nemykin, A.V. Maskaev, M.R. Geraskina, A. Kirschning and V.V. Zhdankin, 2012. Potassium 4‐iodylbenzenesulfonate: Preparation, structure and application as a reagent for oxidative iodination of Arenes. Eur. J. Organic Chem., 2012: 5935-5942.
    CrossRef  |  Direct Link  |  

  65. Yusubov, M.S. and V.V. Zhdankin, 2012. Hypervalent iodine reagents and green chemistry. Curr. Organic Synthesis, 9: 247-272.
    CrossRef  |  Direct Link  |  

  66. Yoshimura, A., M.W. Luedtke and V.V. Zhdankin, 2012. (Tosylimino) phenyl-λ3-iodane as a reagent for the synthesis of methyl carbamates via hofmann rearrangement of aromatic and aliphatic carboxamides. J. Organic Chem., 77: 2087-2091.
    CrossRef  |  Direct Link  |  

  67. Yoshimura, A., K.R. Middleton, M.W. Luedtke, C. Zhu and V.V. Zhdankin, 2012. Hypervalent iodine catalyzed Hofmann rearrangement of carboxamides using oxone as terminal oxidant. J. Organic Chem., 77: 11399-11404.
    CrossRef  |  Direct Link  |  

  68. Yoshimura, A., K.R. Middleton, C. Zhu, V.N. Nemykin and V.V. Zhdankin, 2012. Hypoiodite‐mediated metal‐free catalytic aziridination of alkenes. Angewandte Chem. Int. Edn., 51: 8059-8062.
    CrossRef  |  Direct Link  |  

  69. Zhdankin, V.V., 2011. Organoiodine (V) reagents in organic synthesis. J. Organic Chem., 76:: 1185-1197.
    CrossRef  |  Direct Link  |  

  70. Zeng, X.M., J.M. Chen, A. Yoshimura, K. Middleton and V.V. Zhdankin, 2011. SiO2-supported RuCl3/3-(dichloroiodo) benzoic acid: Green catalytic system for the oxidation of alcohols and sulfides in water. RSC Adv., 1: 973-977.
    Direct Link  |  

  71. Yoshimura, A., V.N. Nemykin and V.V. Zhdankin, 2011. o‐Alkoxyphenyliminoiodanes: Highly efficient reagents for the catalytic aziridination of alkenes and the metal‐free amination of organic substrates. Chem. Eur. J., 17: 10538-10541.
    CrossRef  |  Direct Link  |  

  72. Yoshimura, A., C.T. Banek, M.S. Yusubov, V.N. Nemykin and V.V. Zhdankin, 2011. Preparation, X-ray structure and reactivity of 2-iodylpyridines: Recyclable hypervalent iodine (V) reagents. J. Organic Chem., 76: 3812-3819.
    CrossRef  |  Direct Link  |  

  73. Nemykin, V.N., A.V. Maskaev, M.R. Geraskina, M.S. Yusubov and V.V. Zhdankin, 2011. Preparation and X-ray crystal study of benziodoxaborole derivatives: New hypervalent iodine heterocycles. Inorganic Chem., 50: 11263-11272.
    CrossRef  |  Direct Link  |  

  74. Chen, J.M., X.M. Zeng, K. Middleton, M.S. Yusubov and V.V. Zhdankin, 2011. Preparation and reactivity of polystyrene-supported iodosylbenzene: Convenient recyclable oxidizing reagent and catalyst. Synlett, 11: 1613-1617.
    CrossRef  |  Direct Link  |  

  75. Chen, J.M., X.M. Zeng, K. Middleton and V.V. Zhdankin, 2011. Facile preparation and reactivity of polystyrene-supported (dichloroiodo) benzene: A convenient recyclable reagent for chlorination and oxidation. Tetrahedron Lett., 52: 1952-1955.
    CrossRef  |  Direct Link  |  

  76. Zagulyaeva, A.A., M.S. Yusubov and V.V. Zhdankin, 2010. A general and convenient preparation of [Bis (trifluoroacetoxy) iodo] perfluoroalkanes and [Bis (trifluoroacetoxy) iodo] arenes by oxidation of organic iodides using oxone and trifluoroacetic acid. J. Organic Chem., 75: 2119-2122.
    CrossRef  |  Direct Link  |  

  77. Zagulyaeva, A.A., C.T. Banek, M.S. Yusubov and V.V. Zhdankin, 2010. Hofmann rearrangement of carboxamides mediated by hypervalent iodine species generated in situ from iodobenzene and oxone: Reaction scope and limitations. Organic Lett., 12: 4644-4647.
    CrossRef  |  Direct Link  |  

  78. Yusubov, M.S., V.N. Nemykin and V.V. Zhdankin, 2010. Transition metal-mediated oxidations utilizing monomeric iodosyl-and iodylarene species. Tetrahedron, 66: 5745-5752.
    CrossRef  |  Direct Link  |  

  79. Yusubov, M.S., R.Y. Yusubova, T.V. Funk, K.W. Chi, A. Kirschning and V.V. Zhdankin, 2010. m-Iodosylbenzoic acid as a convenient recyclable hypervalent iodine oxidant for the synthesis of α-iodo ketones by oxidative iodination of ketones. Synthesis, 21: 3681-3685.
    CrossRef  |  Direct Link  |  

  80. Yusubov, M.S. and V.V. Zhdankin, 2010. Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds. Mendeleev Commun., 20: 185-191.
    Direct Link  |  

  81. Yoshimura, A., H.M. Neu, V.N. Nemykin and V.V. Zhdankin, 2010. Metalloporphyrin/Iodine (III)‐cocatalyzed oxygenation of aromatic hydrocarbons. Adv. Synthesis Catalysis, 352: 1455-1460.
    CrossRef  |  Direct Link  |  

  82. Neu, H.M., V.V. Zhdankin and V.N. Nemykin, 2010. Binuclear iron (III) phthalocyanine (μ-oxodimer)/tetrabutylammonium oxone: A powerful catalytic system for oxidation of hydrocarbons in organic solution. Tetrahedron Lett., 51: 6545-6548.
    CrossRef  |  Direct Link  |  

  83. Katritzky, A.R., C.A. Ramsden, J.A. Joule and V.V. Zhdankin, 2010. Handbook of Heterocyclic Chemistry. 3rd Edn., Elsevier, Oxford, ISBN: 9780080958446, Pages: 1010.

  84. Chen, J.M., X.M. Zeng and V.V. Zhdankin, 2010. Preparation and reactivity of polystyrene-supported iodosylbenzene sulfate: An efficient recyclable oxidizing system. Synlett, 18: 2771-2774.
    CrossRef  |  Direct Link  |  

  85. Zhdankin, V.V., 2009. Hypervalent iodine (III) reagents in organic synthesis. ARKIVOC, 1: 1-62.

  86. Yusubov, M.S., R.Y. Yusubova, T.V. Funk, K.W. Chi and V.V. Zhdankin, 2009. Oligomeric Iodosylbenzene Sulfate: A Convenient hypervalent iodine reagent for oxidation of organic sulfides and alkenes. Synthesis, 15: 2505-2508.

  87. Yusubov, M.S., A.A. Zagulyaeva and V.V. Zhdankin, 2009. Iodine (V)/ruthenium (III)‐cocatalyzed oxidations: A highly efficient tandem catalytic system for the oxidation of alcohols and hydrocarbons with Oxone. Chem. A Eur. J., 15: 11091-11094.
    CrossRef  |  Direct Link  |  

  88. Neu, H.M., M.S. Yusubov, V.V. Zhdankin and V.N. Nemykin, 2009. Binuclear Iron (III) phthalocyanine (μ‐Oxodimer)‐catalyzed oxygenation of aromatic hydrocarbons with iodosylbenzene sulfate and iodosylbenzene as the Oxidants. Adv. Synthesis Catalysis, 351: 3168-3174.
    CrossRef  |  Direct Link  |  

  89. Nemykin, V.N., A.Y. Koposov, B.C. Netzel, M.S. Yusubov and V.V. Zhdankin, 2009. Self-assembly of hydroxy (phenyl) iodonium ions in acidic aqueous solution: Preparation and X-ray crystal structures of oligomeric phenyliodine (III) sulfates. Inorganic Chem., 48: 4908-4917.
    CrossRef  |  Direct Link  |  

  90. Mailyan, A.K., I.M. Geraskin, V.N. Nemykin and V.V. Zhdankin, 2009. Preparation, X-ray structure and oxidative reactivity of N-(2-iodylphenyl) tosylamides and 2-iodylphenyl tosylate: Iodylarenes stabilized by ortho-substitution with a sulfonyl group. J. Organic Chem., 74: 8444-8447.
    CrossRef  |  Direct Link  |  

  91. Geraskin, I.M., O. Pavlova, H.M. Neu, M.S. Yusubov, V.N. Nemykin and V.V. Zhdankin, 2009. Comparative reactivity of hypervalent iodine oxidants in metalloporphyrin‐catalyzed oxygenation of hydrocarbons: Iodosylbenzene sulfate and 2‐iodylbenzoic acid ester as safe and convenient alternatives to Iodosylbenzene. Adv. Synthesis Catalysis, 351: 733-737.
    CrossRef  |  Direct Link  |  

  92. Zhdankin, V.V., V.N. Nemykin, R.R. Karimov and Z.G. Kazhkenov, 2008. Preparation and X-ray crystal structure of 2-iodyl-N, N-dialkylaniline oxides: First entry into the heterocyclic system of benziodoxazole. Chem. Commun., 46: 6131-6133.
    CrossRef  |  Direct Link  |  

  93. Zhdankin, V.V., 2008. Heterocycles with Three or Four Heteroatoms Including at Least One Phosphorus. In: Comprehensive Heterocyclic Chemistry III, Katritzky, A.R., C.A. Ramsden, E.F.V. Scriven and R.J.K. Taylor (Eds.). Vol. 6, Elsevier, Oxford, pp: 583-602.

  94. Zhdankin, V.V. and P.J. Stang, 2008. Chemistry of polyvalent iodine. Chem. Rev., 108: 5299-5358.
    CrossRef  |  Direct Link  |  

  95. Yusubov, M.S., T.V. Funk, K.W. Chi, E.H. Cha, G.H. Kim, A. Kirschning and V.V. Zhdankin, 2008. Preparation and X-ray structures of 3-[Bis (trifluoroacetoxy) iodo] benzoic acid and 3-[hydroxy (tosyloxy) iodo] benzoic acid: New recyclable hypervalent iodine reagents. J. Organic Chem., 73: 295-297.
    CrossRef  |  Direct Link  |  

  96. Geraskin, I.M., M.W. Luedtke, H.M. Neu, V.N. Nemykin and V.V. Zhdankin, 2008. Organic iodine (V) compounds as terminal oxidants in iron (III) phthalocyanine catalyzed oxidation of alcohols. Tetrahedron Lett., 49: 7410-7412.
    CrossRef  |  Direct Link  |  

  97. Claeys, D.D., K. Moonen, B.I. Roman, V.N. Nemykin and V.V. Zhdankin et al., 2008. Synthesis of tricyclic phosphonopyrrolidines via IMDAF: Experimental and theoretical investigation of the observed stereoselectivity. J. Organic Chem., 73: 7921-7927.
    CrossRef  |  Direct Link  |  

  98. Zhdankin, V.V., 2007. 31.4.1 product subclass 1: Hypervalent iodoarenes and aryliodonium salts. Sci. Synthesis, Vol. 31. 10.1055/sos-SD-031-00109.
    CrossRef  |  

  99. Yusubov, M.S., M.P. Gilmkhanova, V.V. Zhdankin and A. Kirschning, 2007. m-Iodosylbenzoic acid as a convenient recyclable reagent for highly efficient RuCl3-catalyzed oxidation of alcohols to carbonyl compounds. Synlett, 2007: 563-566.
    CrossRef  |  Direct Link  |  

  100. Yusubov, M.S., E.N. Tveryakova, E.A. Krasnokutskaya, I.A. Perederyna and V.V. Zhdankin, 2007. Solvent‐free iodination of arenes using iodine-silver nitrate combination. Synthetic Commun., 37: 1259-1265.
    CrossRef  |  Direct Link  |  

  101. Stevens, C.V., E. van Meenen, K.G. Masschelein, Y. Eeckhout and W. Hooghe et al., 2007. A copper-catalyzed domino radical cyclization route to benzospiro-indolizidinepyrrolidinones. Tetrahedron Lett., 48: 7108-7111.
    CrossRef  |  Direct Link  |  

  102. Ladziata, U. and V.V. Zhdankin, 2007. N-(2-Iodylphenyl) acylamides-new pentavalent iodine oxidizing reagents. Synlett, 2007: 527-537.
    CrossRef  |  Direct Link  |  

  103. Koposov, A.Y., V.N. Nemykin and V.V. Zhdankin, 2007. (S)-Methyl 2-(2-iodobenzamido) propionate. Acta Crystallographica Sect. E: Struct. Rep. Online, Vol. 63. 10.1107/S160053680705266X.
    CrossRef  |  

  104. Koposov, A.Y., B.C. Netzel, M.S. Yusubov, V.N. Nemykin, A.Y. Nazarenko and V.V. Zhdankin, 2007. Preparation and structure of oligomeric iodosylbenzene sulfate (PhIO)3• SO3: Stable and water‐soluble analog of Iodosylbenzene. Eur. J. Organic Chem., 2007: 4475-4478.
    CrossRef  |  Direct Link  |  

  105. Karimov, R.R., Z.G.M. Kazhkenov, M.J. Modjewski, E.M. Peterson and V.V. Zhdankin, 2007. Preparation and reactivity of polymer-supported 2-iodylphenol ethers, an efficient recyclable oxidizing system. J. Organic Chem., 72: 8149-8151.
    CrossRef  |  Direct Link  |  

  106. Gunasekera, D.S., D.J. Gerold, N.S. Aalderks, J.S. Chandra and C.A. Maanu et al., 2007. Practical synthesis and applications of benzoboroxoles. Tetrahedron, 63: 9401-9405.
    CrossRef  |  Direct Link  |  

  107. Zhdankin, V.V., 2006. 1-Hydroxy-1,2-Benziodoxol-3(1H)-One. In: Encyclopedia of Reagents for Organic Synthesis, Paquette, L.A. (Ed.). John Wiley and Sons Ltd., Chichester, England.

  108. Yusubov, M.S., K.W. Chi, J.Y. Park, R. Karimov and V.V. Zhdankin, 2006. Highly efficient RuCl3-catalyzed disproportionation of (diacetoxyiodo) benzene to iodylbenzene and iodobenzene; leading to the efficient oxidation of alcohols to carbonyl compounds. Tetrahedron Lett., 47: 6305-6308.
    CrossRef  |  Direct Link  |  

  109. Ochiai, M., T. Sueda, K. Miyamoto, P. Kiprof and V.V. Zhdankin, 2006. trans Influences on hypervalent bonding of aryl λ3‐iodanes: Their stabilities and isodesmic reactions of benziodoxolones and benziodazolones. Angewandte Chemie, 118: 8383-8386.
    CrossRef  |  Direct Link  |  

  110. Ladziata, U., J. Willging and V.V. Zhdankin, 2006. Facile preparation and reactivity of polymer-supported N-(2-Iodyl-phenyl)-acylamide, an efficient oxidizing system. Org. Lett., 8: 167-170.
    CrossRef  |  Direct Link  |  

  111. Ladziata, U., J. Carlson and V.V. Zhdankin, 2006. Synthesis and oxidative reactivity of new chiral hypervalent iodine(V) reagents based on (S)-proline. Tetrahedron Lett., 47: 6301-6304.
    CrossRef  |  Direct Link  |  

  112. Ladziata, U. and V.V. Zhdankin, 2006. Hypervalent iodine(V) reagents in organic synthesis. ARKIVOC, 9: 26-58.

  113. Koposov, A.Y., R.R. Karimov, A.A. Pronin, T. Skrupskaya, M.S. Yusubov and V.V. Zhdankin, 2006. RuCl3-catalyzed oxidation of iodoarenes with peracetic acid: New facile preparation of iodylarenes. J. Org. Chem., 71: 9912-9914.
    CrossRef  |  Direct Link  |  

  114. Koposov, A.Y., D.N. Litvinov, V.V. Zhdankin, M.J. Ferguson, R. McDonald and R.R. Tykwinski, 2006. Preparation and reductive decomposition of 2‐iodoxybenzenesulfonic acid. X‐ray crystal structure of 1‐hydroxy‐1H‐1,2,3‐benziodoxathiole 3,3‐dioxide. Eur. J. Org. Chem., 2006: 4791-4795.
    CrossRef  |  Direct Link  |  

  115. Koposov, A Y., R.R. Karimov, I.M. Geraskin, V.N. Nemykin and V.V. Zhdankin, 2006. 2-Iodylphenol ethers: Preparation, X-ray crystal structure, and reactivity of new hypervalent iodine(V) oxidizing reagents. J. Org. Chem., 71: 8452-8458.
    CrossRef  |  Direct Link  |  

  116. Dieltiens, N., D.D. Claeys, V.V. Zhdankin, V.N. Nemykin, B. Allaert, F. Verpoort and C.V. Stevens, 2006. The pyroglutamate hydantoin rearrangement. Eur. J. Org. Chem., 2006: 2649-2660.
    CrossRef  |  Direct Link  |  

  117. Zhdankin, V.V., R.N. Goncharenko, D.N. Litvinov and A.Y. Koposov, 2005. Derivatives of 2-iodoxybenzenesulfonic acid: New pseudocyclic hypervalent iodine reagents. Arkivoc, 4: 8-18.

  118. Zhdankin, V.V., A.Y. Koposov, D.N. Litvinov, M.J. Ferguson, R. McDonald, T. Luu and R.R. Tykwinski, 2005. Esters of 2-iodoxybenzoic acid: Hypervalent iodine oxidizing reagents with a pseudobenziodoxole structure. J. Org. Chem., 70: 6484-6491.
    CrossRef  |  Direct Link  |  

  119. Zhdankin, V.V., 2005. Benziodoxole-based hypervalent iodine reagents in organic synthesis. Curr. Org. Synthesis, 2: 121-145.
    CrossRef  |  Direct Link  |  

  120. Zhdankin, V.V., 2005. 1,2-Benziodoxol-3(1H)-One Derivatives. In: Encyclopedia of Reagents for Organic Synthesis, Paquette, L.A. (Ed.). John Wiley and Sons Ltd., Chichester, England.

  121. Yusubov, M.S., L.A. Drygunova, A.V. Tkachev and V.V. Zhdankind, 2005. Halomethoxylation of monoterpenes using (dichloroiodo)benzene. ARKIVOC, 4: 179-188.
    Direct Link  |  

  122. Ladziata, U., A.Y. Koposov, K.Y. Lo, J. Willging, V.N. Nemykin and V.V. Zhdankin, 2005. Synthesis, structure and chemoselective reactivity of N‐(2‐Iodylphenyl) acylamides: Hypervalent iodine reagents bearing a pseudo‐six‐membered ring scaffold. Angewandte Chemie Int. Edn., 44: 7127-7131.
    CrossRef  |  Direct Link  |  

  123. Koposov, A.Y. and V.V. Zhdankin, 2005. Selective oxidation of sulfides to sulfoxides using IBX-esters. Synthesis, 2005: 22-24.
    CrossRef  |  Direct Link  |  

  124. Koposov, A.Y., V.N. Nemykin and V.V. Zhdankin, 2005. Intra-and intermolecular interactions in the solid state structure of 2-iodylbenzenesulfonamides: A heptacoordinated organic iodine(V) compound. New J. Chem., 29: 998-1000.
    CrossRef  |  Direct Link  |  

  125. Zhdankin, V.V., D.N. Litvinov, A.Y. Koposov, T. Luu, M.J. Ferguson, R. McDonald and R.R. Tykwinski, 2004. Preparation and structure of 2-iodoxybenzoate esters: Soluble and stable periodinane oxidizing reagents. Chem. Commun., 2004: 106-107.
    CrossRef  |  Direct Link  |  

  126. Zhdankin, V.V., 2004. Iodosylbenzene. In: Encyclopedia of Reagents for Organic Synthesis, Paquette, L.A. (Ed.). John Wiley and Sons Ltd., Chichester, England.

  127. Zhdankin, V.V., 2004. Alkynyl Halides and Chalcogenides. In: Comprehensive Organic Functional Group Transformations II, Katritzky, A.R. and R.J.K. Taylor (Eds.). Elsevier, Oxford, pp: 1073-1114.

  128. Yusubov, M.S., L.A. Drygunova and V.V. Zhdankin, 2004. 4,4′-Bis(dichloroiodo)biphenyl and 3-(dichloroiodo)benzoic acid: New recyclable hypervalent iodine reagents for vicinal halomethoxylation of unsaturated compounds. Synthesis, 2004: 2289-2292.
    CrossRef  |  Direct Link  |  

  129. Koposov, A.Y., V.V. Boyarskikh and V.V. Zhdankin, 2004. Amino acid-derived iodobenzene dicarboxylates: Reagents for oxidative conversion of alkenes to amino acid esters. Org. Lett., 6: 3613-3615.
    CrossRef  |  Direct Link  |  

  130. Koposov, A.Y., D.N. Litvinov and V.V. Zhdankin, 2004. 2-Iodoxybenzenesulfamides: New pseudobenziodoxole-based hypervalent iodine reagents. Tetrahedron Lett., 45: 2719-2721.
    CrossRef  |  Direct Link  |  

  131. Zhdankin, V.V., O. Maydanovych, J. Herschbach, J. Bruno, E.D. Matveeva and N.S. Zefirov, 2003. Preparation and chemistry of phosphoranyl-derived iodanes. J. Org. Chem., 68: 1018-1023.
    CrossRef  |  Direct Link  |  

  132. Zhdankin, V.V., A.Y. Koposov, L. Su, V.V. Boyarskikh, B.C. Netzel and V.G. Young, 2003. Synthesis and structure of amino acid-derived benziodazoles: New hypervalent iodine heterocycles. Org. Lett., 5: 1583-1586.
    CrossRef  |  Direct Link  |  

  133. Zhdankin, V.V., A.Y. Koposov, B.C. Netzel, N.V. Yashin, B.P. Rempel, M.J. Ferguson and R.R. Tykwinski, 2003. IBX amides: A new family of hypervalent iodine reagents. Angewandte Chemie Int. Edn., 42: 2194-2196.
    CrossRef  |  Direct Link  |  

  134. Zhdankin, V.V., 2003. Professor Anastasios Varvoglis: A tribute. ARKIVOC, 6: 1-10.

  135. Zhdankin, V.V., 2003. C-C Bond Forming Reactions. In: Topics in Current Chemistry, Wirth, T. (Ed.). Springer-Verlag, Berlin, Heidelberg, pp: 99-136.

  136. Matveeva, E.D., T.A. Podrugina, Y.K. Grishin, V.V. Tkachev, V.V. Zhdankin, S.M. Aldoshin and N.S. Zefirov, 2003. Synthesis and structure of mixed phosphonium-iodonium ylide. Russian J. Org. Chem., 39: 536-541.
    CrossRef  |  Direct Link  |  

  137. Kiprof, P. and V.V. Zhdankin, 2003. Self-assembly of hypervalent iodine through primary and secondary bonding. ARKIVOC, 6: 170-178.

  138. Zhdankin, V.V., O. Maydanovych, J. Herschbach, R. McDonald and R.R. Tykwinski, 2002. Preparation, structure and unexpected chemistry of phosphoranyl-derived benziodoxoles. J. Am. Chem. Soc., 124: 11614-11615.
    CrossRef  |  Direct Link  |  

  139. Zhdankin, V.V., O. Maydanovych, J. Herschbach, J. Bruno, E.D. Matveeva and N.S. Zefirov, 2002. Preparation, structure and chemistry of phosphorane-derived phenyliodonium sulfonates. Tetrahedron Lett., 43: 2359-2361.
    CrossRef  |  Direct Link  |  

  140. Zhdankin, V.V., A.Y. Koposov and N.V. Yashin, 2002. Complexes of hypervalent iodine compounds with nitrogen ligands. Tetrahedron Lett., 43: 5735-5737.
    CrossRef  |  Direct Link  |  

  141. Zhdankin, V.V., 2002. Hypervalent iodine reagents in organic synthesis. Speciality Chem. Magaz., 22: 38-39.

  142. Zhdankin, V.V. and P.J. Stang, 2002. Recent developments in the chemistry of polyvalent iodine compounds. Chem. Rev., 102: 2523-2584.

  143. Pirkuliyev, N.S., V.K. Brel', V.V. Zhdankin and N.S. Zefirov, 2002. Reaction of Fluoro[trifluoromethanesulfonyloxy-λ3-iodanil]benzene with Nitrogen-containing heterocycles. Russian J. Org. Chem., 38: 1224-1225.
    CrossRef  |  Direct Link  |  

  144. Zhdankin, V.V., K.J. Hanson, A.E. Koposov, E. Blomquist and R.R. Tykwinski, 2001. Functionalization of buckminsterfullerene by hypervalent iodine reagents. Mendeleev Commun., 11: 51-52.
    Direct Link  |  

  145. Zhdankin, V.V., A.E. Koposov, J.T. Smart, R.R. Tykwinski, R. McDonald and A. Morales-Izquierdo, 2001. Secondary bonding-directed self-assembly of amino acid derived benziodazoles: Synthesis and structure of novel hypervalent iodine macrocycles. J. Am. Chem. Soc., 123: 4095-4096.
    CrossRef  |  Direct Link  |  

  146. Zhdankin, V.V., P.J. Persichini, R. Cui and Y. Jin, 2000. A convenient synthesis of alkynyliodonium salts from alkynylboronates and hypervalent iodine reagents. Synlett, 2000: 719-721.
    CrossRef  |  Direct Link  |  

  147. Zhdankin, V.V., J.T. Smart, P. Zhao and P. Kiprof, 2000. Synthesis and reactions of amino acid-derived benziodazole oxides: New chiral oxidizing reagents. Tetrahedron Lett., 41: 5299-5302.
    CrossRef  |  Direct Link  |  

  148. Zhdankin, V.V., P.J. Persichini, L. Zhang, S. Fix and P. Kiprof, 1999. Synthesis and structure of benzoboroxoles: Novel organoboron heterocycles. Tetrahedron Lett., 40: 6705-6708.
    CrossRef  |  Direct Link  |  

  149. Zhdankin, V.V., J.A. Callies, K.J. Hanson and J. Bruno, 1999. New alkyliodonium derivatives stabilized by ammonium or phosphonium groups. Tetrahedron Lett., 40: 1839-1842.
    CrossRef  |  Direct Link  |  

  150. Zhdankin, V.V., 1999. Chemistry of hypervalent compounds (Book review). J. Am. Chem. Soc., 121: 6971-6971.

  151. Zhdankin, V.V. and P.J. Stang, 1999. Polycoordinate Iodine Compounds. In: Chemistry of Hypervalent Molecules, Akiba, K. (Ed.). Chapter 11, VCH Publishers, New York, pp: 327-358.

  152. Magerramov, A.M., A.M. Allakhverdiev, Z.I. Akhmedova, R. Caple and V.V. Zhdankin, 1999. New synthesis of tetrahydro-L,4-Thiazine-3-Ones from 1,2-aminopropanethiols and α-chlorocarboxylic acids. Synthetic Commun., 29: 721-728.
    CrossRef  |  Direct Link  |  

  153. Franz, A.H., V.V. Zhdankin, V.V. Samoshin, M.J. Minch, V.G. Young and P.H. Gross, 1999. Structure and conformation of tri-O-acetyl-D-glucal dimer in solid state and in solution. Mendeleev Commun., 9: 45-47.
    Direct Link  |  

  154. Zhdankin, V.V., R.M. Arbit, B.J. Lynch, P. Kiprof and V.G. Young, 1998. Structure and chemistry of hypervalent iodine heterocycles: Acid-catalyzed rearrangement of benziodazol-3-ones to 3-iminiumbenziodoxoles. J. Org. Chem., 63: 6590-6596.
    CrossRef  |  Direct Link  |  

  155. Zhdankin, V.V. and P.J. Stang, 1998. Alkynyliodonium salts in organic synthesis. Tetrahedron, 54: 10927-10966.

  156. Lynch, B.J., V.V. Zhdankin and P. Kiprof, 1998. Theoretical studies of hypervalent iodine compounds. Internet J. Chem., 1: U1-U10.

  157. Zhdankin, V.V., S.A. Erickson and K.J. Hanson, 1997. Preparation, X-ray crystal structure and chemistry of ((Arylsulfonyl)methyl)(phenyl)iodonium triflates. Stable alkyliodonium salts. J. Am. Chem. Soc., 119: 4775-4776.
    CrossRef  |  Direct Link  |  

  158. Zhdankin, V.V., R.M. Arbit, M. McSherry, B. Mismash and V.G. Young, 1997. Structure and chemistry of acetoxybenziodazole. Acid-catalyzed rearrangement of benziodazoles to 3-iminobenziodoxoles. J. Am. Chem. Soc., 119: 7408-7409.
    CrossRef  |  Direct Link  |  

  159. Zhdankin, V.V., M. McSherry, B. Mismash, J.T. Bolz, J.K. Woodward, R.M. Arbit and S. Erickson, 1997. 1-Amido-3-(1H)-1,2-benziodoxoles: Stable amidoiodanes and reagents for direct amidation of organic substrates. Tetrahedron Lett., 38: 21-24.
    CrossRef  |  Direct Link  |  

  160. Zhdankin, V.V., 1997. Chemistry of benziodoxoles. Rev. Heteroatom Chem., 17: 133-151.

  161. Papoutsis, I., S. Spyroudis, A. Varvoglis, J.A. Callies and V.V. Zhdankin, 1997. Novel trifluoroethyliodonium salts from cyclic enaminones and their thermal decomposition. Tetrahedron Lett., 38: 8401-8404.
    CrossRef  |  Direct Link  |  

  162. Zhdankin, V.V., C.J. Kuehl, A.P. Krasutsky, J.T. Bolz and A.J. Simonsen, 1996. 1-(Organosulfonyloxy)-3(1H)-1,2-benziodoxoles: Preparation and reactions with alkynyltrimethylsilanes. J. Org. Chem., 61: 6547-6551.
    CrossRef  |  Direct Link  |  

  163. Zhdankin, V.V., C.J. Kuehl, A.M. Arif and P.J. Stang, 1996. Synthesis and X-ray crystal structure of l-cyano-3,3-bis(trifluoromethyl)-l,3-dihydro-lλ3, 2-benzoiodoxole, a stable cyanoiodolane. Mendeleev Commun., 2: 50-51.
    CrossRef  |  Direct Link  |  

  164. Zhdankin, V.V., C.J. Kuehl and A.J. Simonsen, 1996. Iodosylperfluoroalkanes as reagents for the preparation of perfluoroalkyliodonium salts under aprotic conditions. Main Group Chem., 1: 349-352.
    CrossRef  |  Direct Link  |  

  165. Zhdankin, V.V., C.J. Kuehl and A.J. Simonsen, 1996. 1-[Hydroxy(sulfonyloxy)iodo]-1H,1H-perfluoroalkanes: Stable, fluoroalkyl analogs of Koser's reagent. J. Org. Chem., 61: 8272-8276.
    CrossRef  |  Direct Link  |  

  166. Zhdankin, V.V., A.P. Krasutsky, C.J. Kuehl, A.J. Simonsen, J.K. Woodward, B. Mismash and J.T. Bolz, 1996. Preparation, X-ray crystal structure and chemistry of stable azidoiodinanes derivatives of benziodoxole. J. Am. Chem. Soc., 118: 5192-5197.
    CrossRef  |  Direct Link  |  

  167. Stang, P.J. and V.V. Zhdankin, 1996. Organic polyvalent iodine compounds. Chem. Rev., 96: 1123-1178.

  168. Zhdankin, V.V., C.J. Kuehl, A.P. Krasutsky, J.T. Bolz, B. Mismash, J.K. Woodward and A.J. Simonsen, 1995. 1-Cyano-3-(1H)-1,2-benziodoxols: Stable cyanoiodinanes and efficient reagents for direct N-alkyl cyanation of N,N-dialkylarylamines. Tetrahedron Lett., 36: 7975-7978.
    CrossRef  |  Direct Link  |  

  169. Zhdankin, V.V., C.J. Kuehl and A.J. Simonsen, 1995. 1-[Hydroxy(sulfonyloxy)iodo]-2,2,2-trifluoroethanes, CF3CH2I(OH)OSO2R: Stable, fluoroalkyl analogs of Koser's reagent. Tetrahedron Lett., 36: 2203-2206.
    CrossRef  |  Direct Link  |  

  170. Zhdankin, V.V., 1995. Lithium Phenylethynolate. In: Encyclopedia of Reagents for Organic Synthesis, Paquette, L.A. (Ed.). John Wiley and Sons Ltd., Chichester, England, ISBN: 0471936235, pp: 3156-3157.

  171. Stang, P.J. and V.V. Zhdankin, 1995. Fluorinated Compounds as Reagents. In: Chemistry of Organic Fluorine Compounds II: A Critical Review, Hudlicky, M. and A.E. Pavlath (Eds.). ACS Press, Washington, DC., ISBN: 084122515X, pp: 939-978.

  172. Stang, P.J. and V.V. Zhdankin, 1995. Alkynyl Halides and Chalcogenides. In: Comprehensive Organic Functional Group Transformations, Katritzky, A.R., O. Meth-Cohn and C.W. Rees (Eds.). Pergamon Press, Oxford, ISBN: 008042323X, pp: 1011-1038.

  173. Kuehl, C.J., J.T. Bolz and V.V. Zhdankin, 1995. [Hydroxy(sulfonyloxy)iodo]perfluoroalkanes: New and convenient reagents for the preparation of Fluoroalkyl(aryl)iodonium salts. Synthesis, 1995: 312-316.
    CrossRef  |  Direct Link  |  

  174. Krasutsky, A.P., C.J. Kuehl and V.V. Zhdankin, 1995. Direct azidation of adamantane and norbornane by stable azidoiodinanes. Synlett, 1995: 1081-1082.
    CrossRef  |  Direct Link  |  

  175. Zhdankin, V.V., C.J. Kuehl, J.T. Bolz, M.S. Formaneck and A.J. Simonsen, 1994. Preparation and chemistry of 1-organosulfonyloxy-1,2-benziodoxol-3-(1H)-ones: First example of a stable adduct of 2-iodosobenzoic acid with strong acid. Tetrahedron Lett., 35: 7323-7326.
    CrossRef  |  Direct Link  |  

  176. Zhdankin, V.V., C.J. Kuehl, J.T. Bolz and N.S. Zefirov, 1994. A general synthetic approach to aryl(perfluoroalkyl)iodonium sulfonates by the reaction of [hydroxy(sulfonyloxy)iodo]perfluoroalkanes with arylsilanes. Mendeleev Commun., 4: 165-166.
    CrossRef  |  Direct Link  |  

  177. Zhdankin, V.V., C.J. Kuehl, A.P. Krasutsky, M.S. Formaneck and J.T. Bolz, 1994. Preparation and chemistry of stable azidoiodinanes: 1-Azido-3,3-bis(trifluoromethyl)-3-(1H)-1, 2-enziodoxol and 1-Azido-1,2-benziodoxol-3-(1H)-one. Tetrahedron Lett., 35: 9677-9680.
    CrossRef  |  Direct Link  |  

  178. Zhdankin, V.V. and C. Kuehl, 1994. [Hydroxy(sulfonyloxy)iodo]perfluoroalkanes-new hypervalent iodine species and promising reagents for organic synthesis. Tetrahedron Lett., 35: 1809-1812.
    CrossRef  |  Direct Link  |  

  179. Stang, P.J. and V.V. Zhdankin, 1994. Ynol Ethers and Esters. In: The Chemistry of Triple-Bonded Functional Groups, Supplement C2, Patai, S. (Ed.). John Wiley and Sons Ltd., Chichester, England, ISBN: 047193559X, pp: 1135-1164.

  180. Zhdankin, V.V., M.C. Scheuller and P.J. Stang, 1993. A general approach to aryl(cyano) iodonium triflates-versatile iodonium transfer reagents. Tetrahedron Lett., 34: 6853-6856.
    CrossRef  |  Direct Link  |  

  181. Zhdankin, V.V., 1993. Organic chemistry of noble gases. Russian Chem. Bull., 42: 1763-1771.
    CrossRef  |  Direct Link  |  

  182. Zefirov, N.S., T.M. Kasumov, A.S. Koz'min, V.D. Sorokin, P.J. Stang and V.V. Zhdankin, 1993. Iodosyl fluorosulfate-A new efficient reagent for the direct synthesis of diaryliodonium salts. Synthesis, 1993: 1209-1210.
    CrossRef  |  Direct Link  |  

  183. Stang, P.J. and V.V. Zhdankin, 1993. Preparation and characterization of a macrocyclic tetraaryltetraiodonium compound, cyclo (Ar4I4)4+.cntdot.4X-.A unique, charged, cationic molecular box. J. Am. Chem. Soc., 115: 9808-9809.
    CrossRef  |  Direct Link  |  

  184. Gallop, P.M., M.A. Paz, R. Fluckiger, P.J. Stang, V.V. Zhdankin and R.R. Tykwinski, 1993. Highly effective PQQ inhibition by alkynyl and aryl mono-and diiodonium salts. J. Am. Chem. Soc., 115: 11702-11704.
    CrossRef  |  Direct Link  |  

  185. Fine, R., 1986. Historical Introduction. In: Narcissism, the Self, and Society, Fine, R. (Ed.), Columbia University Press, Columbia, ISBN: 9780231886901, pp: 1-36.
    CrossRef  |  Direct Link  |  
Member since April, 2018