Dr. Viktor V. Zhdankin
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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

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Area of Interest:

Chemistry
100%
Sustainable Chemistry
62%
Organic Chemistry
90%
Catalysis Chemistry
75%
Heterocycles
55%

Research Publications in Numbers

Books
7
Chapters
0
Articles
327
Abstracts
0

Selected Publications

  1. Zhdankin, V., 2022. Introduction to hypervalent iodine chemistry. Arkivoc, 2022: 1-6.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  8. Yusubov, M.S. and V.V. Zhdankin, 2021. Zefirov's reagent and related hypervalent iodine triflates. Mendeleev Commun., 31: 282-287.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  15. Zhdankin, V.V., 2020. Hypervalent iodine compounds: Reagents of the future. Arkivoc, 2020: 1-11.
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  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.
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  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.
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  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.
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  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.
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  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.
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  21. Zhdankin, V.V. and K. Muniz, 2017. Editorial for the special issue on hypervalent iodine reagents. J. Org. Chem., 82: 11667-11668.
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  22. Zhdankin, V.V. and A.N. Pestryakov, 2017. Special issue on organic synthesis and hydrocarbon feedstock refining. Curr. Organic Synthesis, 14: 322-322.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  36. Yoshimura, A. and V.V. Zhdankin, 2016. Advances in synthetic applications of hypervalent iodine compounds. Chem. Rev., 116: 3328-3435.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  65. Yusubov, M.S. and V.V. Zhdankin, 2012. Hypervalent iodine reagents and green chemistry. Curr. Organic Synthesis, 9: 247-272.
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  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.
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  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.
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  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.
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  69. Zhdankin, V.V., 2011. Organoiodine (V) reagents in organic synthesis. J. Organic Chem., 76:: 1185-1197.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  102. Ladziata, U. and V.V. Zhdankin, 2007. N-(2-Iodylphenyl) acylamides-new pentavalent iodine oxidizing reagents. Synlett, 2007: 527-537.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  119. Zhdankin, V.V., 2005. Benziodoxole-based hypervalent iodine reagents in organic synthesis. Curr. Org. Synthesis, 2: 121-145.
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  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.
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  123. Koposov, A.Y. and V.V. Zhdankin, 2005. Selective oxidation of sulfides to sulfoxides using IBX-esters. Synthesis, 2005: 22-24.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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  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.
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