| Year |
Citation |
Score |
| 2024 |
Yoshimura A, Ngo K, Mironova IA, Gardner ZS, Rohde GT, Ogura N, Ueki A, Yusubov MS, Saito A, Zhdankin VV. Pseudocyclic Arylbenziodoxaboroles as Water-Triggered Aryne Precursors in Reactions with Organic Sulfides. Organic Letters. 26: 1891-1895. PMID 38408024 DOI: 10.1021/acs.orglett.4c00197 |
0.353 |
|
| 2023 |
Mironova IA, Noskov DM, Yoshimura A, Yusubov MS, Zhdankin VV. Aryl-, Akynyl-, and Alkenylbenziodoxoles: Synthesis and Synthetic Applications. Molecules (Basel, Switzerland). 28. PMID 36903382 DOI: 10.3390/molecules28052136 |
0.339 |
|
| 2021 |
Shea MT, Rohde GT, Vlasenko YA, Postnikov PS, Yusubov MS, Zhdankin VV, Saito A, Yoshimura A. Convenient Synthesis of Benziodazolone: New Reagents for Direct Esterification of Alcohols and Amidation of Amines. Molecules (Basel, Switzerland). 26. PMID 34885939 DOI: 10.3390/molecules26237355 |
0.365 |
|
| 2021 |
Antonkin NS, Vlasenko YA, Yoshimura A, Smirnov VI, Borodina TN, Zhdankin VV, Yusubov MS, Shafir A, Postnikov PS. Preparation and Synthetic Applicability of Imidazole-Containing Cyclic Iodonium Salts. The Journal of Organic Chemistry. PMID 33944564 DOI: 10.1021/acs.joc.1c00483 |
0.412 |
|
| 2020 |
Zhdankin VV. Hypervalent iodine compounds: reagents of the future Arkivoc. 2020: 1-11. DOI: 10.24820/Ark.5550190.P011.145 |
0.32 |
|
| 2020 |
Yoshimura A, Saito A, Yusubov MS, Zhdankin VV. Synthesis of Oxazoline and Oxazole Derivatives by Hypervalent-Iodine-Mediated Oxidative Cycloaddition Reactions Synthesis. 52: 2299-2310. DOI: 10.1055/S-0040-1707122 |
0.443 |
|
| 2020 |
Yusubov MS, Postnikov P, Yoshimura A, Zhdankin VV. Benziodoxole-Derived Organosulfonates: The Strongest Hypervalent Iodine Electrophiles and Oxidants Synlett. 31: 315-326. DOI: 10.1055/S-0039-1690761 |
0.473 |
|
| 2019 |
Yusubov MS, Soldatova NS, Postnikov PS, Valiev RR, Yoshimura A, Wirth T, Nemykin VN, Zhdankin VV. 2-Iodoxybenzoic acid ditriflate: the most powerful hypervalent iodine(v) oxidant. Chemical Communications (Cambridge, England). PMID 31209449 DOI: 10.1039/C9Cc04203B |
0.432 |
|
| 2019 |
Yoshimura A, Makitalo CL, Jarvi ME, Shea MT, Postnikov PS, Rohde GT, Zhdankin VV, Saito A, Yusubov MS. Sulfonylimino Group Transfer Reaction Using Imino-λ³-iodanes with I₂ as Catalyst Under Metal-free Conditions. Molecules (Basel, Switzerland). 24. PMID 30862025 DOI: 10.3390/Molecules24050979 |
0.402 |
|
| 2019 |
Yoshimura A, Yusubov MS, Zhdankin VV. Iodonium imides in organic synthesis Arkivoc. 2019: 228-255. DOI: 10.24820/Ark.5550190.P010.975 |
0.308 |
|
| 2019 |
Peng HC, Bryan J, Henson W, Zhdankin VV, Gandhi K, David S. New, Milder Hypervalent Iodine Oxidizing Agent: Using μ-Oxodi(phenyliodanyl) Diacetate, a (Diacetoxyiodo)benzene Derivative, in the Synthesis of Quinones Journal of Chemical Education. 96: 2622-2627. DOI: 10.1021/Acs.Jchemed.8B00636 |
0.384 |
|
| 2019 |
Yoshimura A, Jarvi ME, Shea MT, Makitalo CL, Rohde GT, Yusubov MS, Saito A, Zhdankin VV. Hypervalent Iodine(III) Reagent Mediated Regioselective Cycloaddition of Aldoximes with Enaminones European Journal of Organic Chemistry. 2019: 6682-6689. DOI: 10.1002/Ejoc.201901258 |
0.358 |
|
| 2018 |
Vlasenko YA, Postnikov PS, Trusova ME, Shafir A, Zhdankin VV, Yoshimura A, Yusubov MS. Synthesis of five-membered iodine-nitrogen heterocycles from benzimidazole-based iodonium salts. The Journal of Organic Chemistry. PMID 30205009 DOI: 10.1021/Acs.Joc.8B01995 |
0.456 |
|
| 2018 |
Yoshimura A, Shea MT, Guselnikova O, Postnikov PS, Rohde GT, Saito A, Yusubov MS, Nemykin VN, Zhdankin VV. Preparation and structure of phenolic aryliodonium salts. Chemical Communications (Cambridge, England). PMID 30152483 DOI: 10.1039/C8Cc06211K |
0.451 |
|
| 2018 |
Mironova IA, Postnikov PS, Yusubova RY, Yoshimura A, Wirth T, Zhdankin VV, Nemykin VN, Yusubov MS. Preparation and X-ray structure of 2-iodoxybenzenesulfonic acid (IBS) - a powerful hypervalent iodine(V) oxidant. Beilstein Journal of Organic Chemistry. 14: 1854-1858. PMID 30112090 DOI: 10.3762/Bjoc.14.159 |
0.416 |
|
| 2018 |
Yoshimura A, Shea MT, Makitalo CL, Jarvi ME, Rohde GT, Saito A, Yusubov MS, Zhdankin VV. Preparation, structure, and reactivity of bicyclic benziodazole: a new hypervalent iodine heterocycle. Beilstein Journal of Organic Chemistry. 14: 1016-1020. PMID 29977373 DOI: 10.3762/Bjoc.14.87 |
0.496 |
|
| 2018 |
Yoshimura A, Saito A, Zhdankin VV. Iodonium Salts as Benzyne Precursors. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29797627 DOI: 10.1002/Chem.201802111 |
0.413 |
|
| 2018 |
Soldatova N, Postnikov P, Kukurina O, Zhdankin VV, Yoshimura A, Wirth T, Yusubov MS. One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone-sulfuric acid. Beilstein Journal of Organic Chemistry. 14: 849-855. PMID 29719579 DOI: 10.3762/Bjoc.14.70 |
0.451 |
|
| 2018 |
Shimizu H, Yoshimura A, Noguchi K, Nemykin VN, Zhdankin VV, Saito A. Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents. Beilstein Journal of Organic Chemistry. 14: 531-536. PMID 29623114 DOI: 10.3762/Bjoc.14.39 |
0.461 |
|
| 2018 |
Podrezova EV, Larkina MS, Belousov MV, Kirschning A, Zhdankin VV, Yusubov MS. Expedient Synthesis of Long-Chain ω-Substituted Fatty Acids and Esters from Cyclic Ketones Using Iodine and Hydrogen Peroxide Synthesis. 50: 4081-4088. DOI: 10.1055/S-0036-1591598 |
0.415 |
|
| 2018 |
Uraoka S, Shinohara I, Shimizu H, Noguchi K, Yoshimura A, Zhdankin VV, Saito A. Cover Feature: Hetero Diels–Alder Reaction and Ene Reaction of Acylnitroso Species in situ Generated by Hypoiodite Catalysis (Eur. J. Org. Chem. 45/2018) European Journal of Organic Chemistry. 2018: 6192-6192. DOI: 10.1002/Ejoc.201801700 |
0.346 |
|
| 2018 |
Uraoka S, Shinohara I, Shimizu H, Noguchi K, Yoshimura A, Zhdankin VV, Saito A. Hetero Diels–Alder Reaction and Ene Reaction of Acylnitroso Species in situ Generated by Hypoiodite Catalysis European Journal of Organic Chemistry. 2018: 6199-6203. DOI: 10.1002/Ejoc.201801340 |
0.353 |
|
| 2018 |
Dieltiens N, Claeys DD, Zhdankin VV, Nemykin VN, Allaert B, Verpoort F, Stevens CV. The Pyroglutamate Hydantoin Rearrangement European Journal of Organic Chemistry. 2018: 3372-3372. DOI: 10.1002/Ejoc.201800986 |
0.301 |
|
| 2018 |
Yusubov MS, Soldatova NS, Postnikov PS, Valiev RR, Svitich DY, Yusubova RY, Yoshimura A, Wirth T, Zhdankin VV. Reactions of 1‐Arylbenziodoxolones with Azide Anion: Experimental and Computational Study of Substituent Effects European Journal of Organic Chemistry. 2018: 640-647. DOI: 10.1002/Ejoc.201701595 |
0.397 |
|
| 2018 |
Yoshimura A, Saito A, Zhdankin VV. Frontispiece: Iodonium Salts as Benzyne Precursors Chemistry: a European Journal. 24. DOI: 10.1002/Chem.201885763 |
0.325 |
|
| 2017 |
Zhdankin V, Yoshimura A, Fuchs J, Middleton K, Maskaev A, Rohde G, Saito A, Postnikov P, Yusubov M, Nemykin V. Pseudocyclic Arylbenziodoxaboroles: Efficient Benzyne Precursors Triggered by Water at Room Temperature. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28981177 DOI: 10.1002/Chem.201704393 |
0.435 |
|
| 2017 |
Yoshimura A, Nguyen KC, Rohde GT, Postnikov PS, Yusubov MS, Zhdankin VV. Hypervalent Iodine Reagent Mediated Oxidative Heterocyclization of Aldoximes with Heterocyclic Alkenes. The Journal of Organic Chemistry. PMID 28730819 DOI: 10.1021/Acs.Joc.7B01462 |
0.484 |
|
| 2017 |
Yagyu T, Takemoto Y, Yoshimura A, Zhdankin VV, Saito A. Iodine(III)-Catalyzed Formal [2 + 2 + 1] Cycloaddition Reaction for Metal-Free Construction of Oxazoles. Organic Letters. PMID 28471179 DOI: 10.1021/Acs.Orglett.7B00742 |
0.386 |
|
| 2017 |
Soldatova N, Postnikov P, Kukurina O, Zhdankin VV, Yoshimura A, Wirth T, Yusubov MS. Facile One-Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone. Chemistryopen. 6: 18-20. PMID 28168145 DOI: 10.1002/Open.201600129 |
0.471 |
|
| 2017 |
Singh GS, Sudheesh S, Keroletswe N, Zhdankin VV. Recent applications of aziridine ring expansion reactions in heterocyclic synthesis Arkivoc. 2018: 50-113. DOI: 10.24820/Ark.5550190.P010.288 |
0.401 |
|
| 2017 |
Yoshimura A, Nguyen KC, Nemykin VN, Zhdankin VV. Preparation, structure, and oxidative reactivity of (dichloroiodo)pyridines: recyclable hypervalent iodine reagents Arkivoc. 2018: 40-49. DOI: 10.24820/Ark.5550190.P010.279 |
0.435 |
|
| 2017 |
Suwiński JW, Zhdankin VV. cine- and tele-Substitution reactions: review of work from 2002-2016 Arkivoc. 2017: 402-435. DOI: 10.24820/Ark.5550190.P010.215 |
0.339 |
|
| 2017 |
Verbitskiy EV, Rusinov GL, Charushin VN, Zhdankin VV. Diazatriphenylenes and their thiophene analogues: synthesis and applications Arkivoc. 2017: 356-401. DOI: 10.24820/Ark.5550190.P010.190 |
0.327 |
|
| 2017 |
Romanenko VD, Kukhar VP, Zhdankin VV. Phosphonate analogues of nucleoside polyphosphates Arkivoc. 2018: 1-49. DOI: 10.24820/Ark.5550190.P010.183 |
0.32 |
|
| 2017 |
Yoshimura A, Zhdankin VV. Oxidative cyclizations of oximes using hypervalent iodine reagents Arkivoc. 2017: 99-116. DOI: 10.24820/Ark.5550190.P010.013 |
0.427 |
|
| 2017 |
Ibrahim-Ouali M, Dumur F, Zhdankin VV. Copper-catalyzed steroid reactions Arkivoc. 2017: 202-256. DOI: 10.24820/Ark.5550190.P009.986 |
0.367 |
|
| 2017 |
Moradi R, Ziarani GM, Lashgari N, Zhdankin VV. Recent applications of isatin in the synthesis of organic compounds Arkivoc. 2017: 148-201. DOI: 10.24820/Ark.5550190.P009.980 |
0.337 |
|
| 2017 |
Saito A, Zhdankin VV. Metal-free syntheses of oxazoles and their analogues based on λ3-iodane-mediated cycloisomerization/functionalization reactions or [2+2+1] cycloaddition type reactions Arkivoc. 2017: 84-98. DOI: 10.24820/Ark.5550190.P009.965 |
0.369 |
|
| 2017 |
Zhang C, Zhdankin VV. Application of fluoroform in trifluoromethylation and difluoromethylation reactions Arkivoc. 2017: 67-83. DOI: 10.24820/Ark.5550190.P009.884 |
0.344 |
|
| 2017 |
Morozova MA, Yusubov MS, Kratochvil B, Eigner V, Bondarev AA, Yoshimura A, Saito A, Zhdankin VV, Trusova ME, Postnikov PS. Regioselective Zn(OAc)2-catalyzed azide–alkyne cycloaddition in water: the green click-chemistry Organic Chemistry Frontiers. 4: 978-985. DOI: 10.1039/C6Qo00787B |
0.371 |
|
| 2017 |
Baba T, Takahashi S, Kambara Y, Yoshimura A, Nemykin VN, Zhdankin VV, Saito A. Development of Imino-λ3
-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions Advanced Synthesis & Catalysis. 359: 3860-3864. DOI: 10.1002/Adsc.201700934 |
0.35 |
|
| 2017 |
Yusubov MS, Postnikov PS, Yusubova RY, Yoshimura A, Jürjens G, Kirschning A, Zhdankin VV. 2-Iodoxybenzoic Acid Tosylates: the Alternative to Dess–Martin Periodinane Oxidizing Reagents Advanced Synthesis & Catalysis. 359: 3207-3216. DOI: 10.1002/Adsc.201700776 |
0.455 |
|
| 2017 |
Okamura Y, Sato D, Yoshimura A, Zhdankin VV, Saito A. Iodine(III)‐Mediated/Catalyzed Cycloisomerization–Amination Sequence of N‐Propargyl Carboxamides Advanced Synthesis & Catalysis. 359: 3243-3247. DOI: 10.1002/Adsc.201700587 |
0.333 |
|
| 2016 |
Zhdankin V, Yoshimura A, Klasen S, Shea M, Nguyen K, Rohde G, Saito A, Postnikov P, Yusubov M, Nemykin V. Preparation, Structure, and Reactivity of Pseudocyclic Benziodoxole Tosylates: New Hypervalent Iodine Oxidants and Electrophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27794175 DOI: 10.1002/Chem.201604475 |
0.512 |
|
| 2016 |
Yoshimura A, Yusubov MS, Zhdankin VV. Synthetic applications of pseudocyclic hypervalent iodine compounds. Organic & Biomolecular Chemistry. 14: 4771-81. PMID 27143521 DOI: 10.1039/C6Ob00773B |
0.453 |
|
| 2016 |
Yoshimura A, Zhdankin VV. Advances in Synthetic Applications of Hypervalent Iodine Compounds. Chemical Reviews. 116: 3328-435. PMID 26861673 DOI: 10.1021/Acs.Chemrev.5B00547 |
0.445 |
|
| 2016 |
Yoshimura A, Zhdankin V. Oxidation of sulfides using recyclable pseudocyclic benziodoxole triflate Arkivoc. 2017: 32-40. DOI: 10.3998/Ark.5550190.P009.893 |
0.371 |
|
| 2016 |
Yusubov MS, Yoshimura A, Zhdankin VV. Iodonium ylides in organic synthesis Arkivoc. 2016: 342-374. DOI: 10.3998/Ark.5550190.P009.732 |
0.31 |
|
| 2016 |
Bozorov K, Zhao J, Aisa HA, Zhdankin VV. Recent advances in ipso-nitration reactions Arkivoc. 2017: 41-66. DOI: 10.24820/Ark.5550190.P009.852 |
0.352 |
|
| 2016 |
Mironova IA, Yusubova RY, Kukurina OS, Yusubov MS, Zhdankin VV. Potassium 4-iodylbenzenesulfonate (PIBS): An efficient recyclable hypervalent iodine reagent for iodo-functionalization of alkenes, alkynes and ketones Current Organic Synthesis. 13: 629-637. DOI: 10.2174/1570179413666151218204056 |
0.354 |
|
| 2016 |
Soldatova N, Postnikov P, Troyan AA, Yoshimura A, Yusubov MS, Zhdankin VV. Mild and efficient synthesis of iodylarenes using Oxone as oxidant Tetrahedron Letters. 57: 4254-4256. DOI: 10.1016/J.Tetlet.2016.08.038 |
0.421 |
|
| 2016 |
Zhdankin VV. Chapter Three - Hypervalent Heterocycles Advances in Heterocyclic Chemistry. 119: 57-79. DOI: 10.1016/Bs.Aihch.2015.11.001 |
0.321 |
|
| 2016 |
Asari N, Takemoto Y, Shinomoto Y, Yagyu T, Yoshimura A, Zhdankin VV, Saito A. Catalytic Cycloisomerization–Fluorination Sequence of N‐Propargyl Amides by Iodoarene/HF⋅Pyridine/Selectfluor Systems Asian Journal of Organic Chemistry. 5: 1314-1317. DOI: 10.1002/Ajoc.201600383 |
0.369 |
|
| 2016 |
Yoshimura A, Nguyen KC, Klasen SC, Postnikov PS, Yusubov MS, Saito A, Nemykin VN, Zhdankin VV. Hypervalent Iodine-Catalyzed Synthesis of 1,2,4-Oxadiazoles from Aldoximes and Nitriles Asian Journal of Organic Chemistry. 5: 1128-1133. DOI: 10.1002/Ajoc.201600247 |
0.452 |
|
| 2016 |
Yoshimura A, Nguyen KC, Rohde GT, Saito A, Yusubov MS, Zhdankin VV. Oxidative Cycloaddition of Aldoximes with Maleimides using Catalytic Hydroxy(aryl)iodonium Species Advanced Synthesis and Catalysis. 358: 2340-2344. DOI: 10.1002/Adsc.201600331 |
0.435 |
|
| 2015 |
Shinomoto Y, Yoshimura A, Shimizu H, Yamazaki M, Zhdankin VV, Saito A. Tetra-n-butylammonium Iodide Catalyzed C-H Azidation of Aldehydes with Thermally Stable Azidobenziodoxolone. Organic Letters. PMID 26492530 DOI: 10.1021/Acs.Orglett.5B02543 |
0.331 |
|
| 2015 |
Postnikov PS, Guselnikova OA, Yusubov MS, Yoshimura A, Nemykin VN, Zhdankin VV. Preparation and X-ray Structural Study of Dibenziodolium Derivatives. The Journal of Organic Chemistry. 80: 5783-8. PMID 25951091 DOI: 10.1021/Acs.Joc.5B00741 |
0.433 |
|
| 2015 |
Yoshimura A, Nguyen KC, Klasen SC, Saito A, Nemykin VN, Zhdankin VV. Preparation, structure, and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent. Chemical Communications (Cambridge, England). 51: 7835-8. PMID 25854194 DOI: 10.1039/C5Cc02009C |
0.46 |
|
| 2015 |
Yoshimura A, Koski SR, Fuchs JM, Saito A, Nemykin VN, Zhdankin VV. Saccharin-based μ-oxo imidoiodane: a readily available and highly reactive reagent for electrophilic amination. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5328-31. PMID 25694131 DOI: 10.1002/Chem.201500335 |
0.458 |
|
| 2015 |
Yusubov MS, Zhdankin VV. Iodine catalysis: A green alternative to transition metals in organic chemistry and technology Resource-Efficient Technologies. 1: 49-67. DOI: 10.1016/J.Reffit.2015.06.001 |
0.412 |
|
| 2015 |
Zhdankin VV. Chapter One – Iodine Heterocycles Advances in Heterocyclic Chemistry. 115: 1-91. DOI: 10.1016/Bs.Aihch.2015.03.003 |
0.422 |
|
| 2015 |
Yusubov MS, Svitich DY, Yoshimura A, Kastern BJ, Nemykin VN, Zhdankin VV. Preparation, X-ray Structure, and Reactivity of Triisopropylsilyl-Substituted Aryliodonium Salts European Journal of Organic Chemistry. 2015: 4831-4834. DOI: 10.1002/Ejoc.201500535 |
0.44 |
|
| 2015 |
Saito A, Kambara Y, Yagyu T, Noguchi K, Yoshimura A, Zhdankin VV. Metal-Free [2+2+1] annulation of alkynes, nitriles and nitrogen atoms from iminoiodanes for synthesis of highly substituted imidazoles Advanced Synthesis and Catalysis. 357: 667-671. DOI: 10.1002/Adsc.201500032 |
0.318 |
|
| 2014 |
Ivanov AS, Popov IA, Boldyrev AI, Zhdankin VV. The I=X (X=O,N,C) double bond in hypervalent iodine compounds: is it real? Angewandte Chemie (International Ed. in English). 53: 9617-21. PMID 25045143 DOI: 10.1002/Anie.201405142 |
0.346 |
|
| 2014 |
Yoshimura A, Koski SR, Kastern BJ, Fuchs JM, Jones TN, Yusubova RY, Nemykin VN, Zhdankin VV. Hypoiodite-mediated cyclopropanation of alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 5895-8. PMID 24687271 DOI: 10.1002/Chem.201402372 |
0.362 |
|
| 2014 |
Yusubov MS, Celik C, Geraskina MR, Yoshimura A, Zhdankin VV, Nemykin VN. Binuclear iron(III) octakis(perfluorophenyl)tetraazaporphyrin μ-oxodimer: A highly efficient catalyst for biomimetic oxygenation reactions Tetrahedron Letters. 55: 5687-5690. DOI: 10.1016/J.Tetlet.2014.08.070 |
0.365 |
|
| 2014 |
Zhdankin VV, Protasiewicz JD. Development of new hypervalent iodine reagents with improved properties and reactivity by redirecting secondary bonds at iodine center Coordination Chemistry Reviews. 275: 54-62. DOI: 10.1016/J.Ccr.2014.04.007 |
0.445 |
|
| 2014 |
Yoshimura A, Todora AD, Kastern BJ, Koski SR, Zhdankin VV. Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone European Journal of Organic Chemistry. 2014: 5149-5152. DOI: 10.1002/Ejoc.201402756 |
0.468 |
|
| 2014 |
Yoshimura A, Jones TN, Yusubov MS, Zhdankin VV. Hypoiodite‐Mediated Catalytic Cyclopropanation of Alkenes with Malononitrile Advanced Synthesis & Catalysis. 356: 3336-3340. DOI: 10.1002/Adsc.201400627 |
0.335 |
|
| 2013 |
Yusubov MS, Svitich DY, Yoshimura A, Nemykin VN, Zhdankin VV. 2-Iodoxybenzoic acid organosulfonates: preparation, X-ray structure and reactivity of new, powerful hypervalent iodine(V) oxidants. Chemical Communications (Cambridge, England). 49: 11269-71. PMID 24153437 DOI: 10.1039/C3Cc47090C |
0.427 |
|
| 2013 |
Yoshimura A, Middleton KR, Todora AD, Kastern BJ, Koski SR, Maskaev AV, Zhdankin VV. Hypervalent iodine catalyzed generation of nitrile oxides from oximes and their cycloaddition with alkenes or alkynes. Organic Letters. 15: 4010-3. PMID 23865434 DOI: 10.1021/Ol401815N |
0.464 |
|
| 2013 |
Yoshimura A, Zhu C, Middleton KR, Todora AD, Kastern BJ, Maskaev AV, Zhdankin VV. Hypoiodite mediated synthesis of isoxazolines from aldoximes and alkenes using catalytic KI and Oxone as the terminal oxidant Chemical Communications. 49: 4800-4802. PMID 23609208 DOI: 10.1039/C3Cc41164H |
0.471 |
|
| 2013 |
Yusubov MS, Yusubova RY, Nemykin VN, Zhdankin VV. Preparation and X-ray structural study of 1-arylbenziodoxolones. The Journal of Organic Chemistry. 78: 3767-73. PMID 23480389 DOI: 10.1021/Jo400212U |
0.429 |
|
| 2012 |
Yoshimura A, Middleton KR, Luedtke MW, Zhu C, Zhdankin VV. Hypervalent iodine catalyzed Hofmann rearrangement of carboxamides using oxone as terminal oxidant. The Journal of Organic Chemistry. 77: 11399-404. PMID 23176018 DOI: 10.1021/Jo302375M |
0.477 |
|
| 2012 |
Zhu C, Yoshimura A, Solntsev P, Ji L, Wei Y, Nemykin VN, Zhdankin VV. New highly soluble dimedone-derived iodonium ylides: preparation, X-ray structure, and reaction with carbodiimide leading to oxazole derivatives. Chemical Communications (Cambridge, England). 48: 10108-10. PMID 22955183 DOI: 10.1039/C2Cc35708A |
0.418 |
|
| 2012 |
Zhu C, Yoshimura A, Ji L, Wei Y, Nemykin VN, Zhdankin VV. Design, preparation, X-ray crystal structure, and reactivity of o-alkoxyphenyliodonium bis(methoxycarbonyl)methanide, a highly soluble carbene precursor. Organic Letters. 14: 3170-3. PMID 22625654 DOI: 10.1021/Ol301268J |
0.434 |
|
| 2012 |
Yoshimura A, Luedtke MW, Zhdankin VV. (Tosylimino)phenyl-λ3-iodane as a reagent for the synthesis of methyl carbamates via Hofmann rearrangement of aromatic and aliphatic carboxamides. The Journal of Organic Chemistry. 77: 2087-91. PMID 22304475 DOI: 10.1021/Jo300007C |
0.479 |
|
| 2012 |
Yusubov MSo, Zhdankin VV. Hypervalent iodine reagents and green chemistry Current Organic Synthesis. 9: 247-272. DOI: 10.2174/157017912799829021 |
0.376 |
|
| 2012 |
Zhu C, Yoshimura A, Wei Y, Nemykin VN, Zhdankin VV. Facile preparation and reactivity of bifunctional ionic liquid-supported hypervalent iodine reagent: a convenient recyclable reagent for catalytic oxidation Tetrahedron Letters. 53: 1438-1444. DOI: 10.1016/J.Tetlet.2012.01.053 |
0.43 |
|
| 2012 |
Yusubov MS, Yusubova RY, Nemykin VN, Maskaev AV, Geraskina MR, Kirschning A, Zhdankin VV. Potassium 4-iodylbenzenesulfonate: Preparation, structure, and application as a reagent for oxidative iodination of arenes European Journal of Organic Chemistry. 5935-5942. DOI: 10.1002/Ejoc.201201064 |
0.451 |
|
| 2011 |
Nemykin VN, Maskaev AV, Geraskina MR, Yusubov MS, Zhdankin VV. Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles. Inorganic Chemistry. 50: 11263-72. PMID 21988373 DOI: 10.1021/Ic201922N |
0.403 |
|
| 2011 |
Yoshimura A, Banek CT, Yusubov MS, Nemykin VN, Zhdankin VV. Preparation, X-ray structure, and reactivity of 2-iodylpyridines: recyclable hypervalent iodine(V) reagents. The Journal of Organic Chemistry. 76: 3812-9. PMID 21462949 DOI: 10.1021/Jo200163M |
0.441 |
|
| 2011 |
Zhdankin VV. Organoiodine(V) reagents in organic synthesis. The Journal of Organic Chemistry. 76: 1185-97. PMID 21247180 DOI: 10.1021/Jo1024738 |
0.401 |
|
| 2011 |
Yusubov MS, Maskaev AV, Zhdankin VV. Iodonium salts in organic synthesis Arkivoc. 2011: 370-409. DOI: 10.3998/Ark.5550190.0012.107 |
0.423 |
|
| 2011 |
Chen JM, Zeng XM, Middleton K, Yusubov MS, Zhdankin VV. Polystyrene-Supported Iodosylbenzene as an Oxidizing Reagent Synfacts. 2011: 1135-1135. DOI: 10.1055/S-0030-1261095 |
0.366 |
|
| 2011 |
Chen J, Zeng X, Middleton K, Yusubov MS, Zhdankin VV. Preparation and Reactivityof Polystyrene-Supported Iodosylbenzene: Convenient RecyclableOxidizing Reagent and Catalyst Synlett. 2011: 1613-1617. DOI: 10.1055/S-0030-1260788 |
0.418 |
|
| 2011 |
Zeng XM, Chen JM, Yoshimura A, Middleton K, Zhdankin VV. SiO 2-supported RuCl 3/3-(dichloroiodo)benzoic acid: Green catalytic system for the oxidation of alcohols and sulfides in water Rsc Advances. 1: 973-977. DOI: 10.1039/C1Ra00635E |
0.438 |
|
| 2011 |
Zeng XM, Chen JM, Middleton K, Zhdankin VV. Recyclable silica-supported iodoarene-RuCl3 bifunctional catalysts for oxidation of alcohols and alkylarenes Tetrahedron Letters. 52: 5652-5655. DOI: 10.1016/J.Tetlet.2011.08.097 |
0.41 |
|
| 2011 |
Chen J, Zeng X, Middleton K, Zhdankin VV. Facile preparation and reactivity of polystyrene-supported (dichloroiodo)benzene: a convenient recyclable reagent for chlorination and oxidation Tetrahedron Letters. 52: 1952-1955. DOI: 10.1016/J.Tetlet.2011.02.065 |
0.468 |
|
| 2010 |
Zagulyaeva AA, Banek CT, Yusubov MS, Zhdankin VV. Hofmann rearrangement of carboxamides mediated by hypervalent iodine species generated in situ from iodobenzene and oxone: reaction scope and limitations. Organic Letters. 12: 4644-7. PMID 20843092 DOI: 10.1021/Ol101993Q |
0.447 |
|
| 2010 |
Zagulyaeva AA, Yusubov MS, Zhdankin VV. 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. The Journal of Organic Chemistry. 75: 2119-22. PMID 20163086 DOI: 10.1021/Jo902733F |
0.384 |
|
| 2010 |
Chen J, Zeng X, Zhdankin VV. Preparation and reactivity of polystyrene-supported iodosylbenzene sulfate: An efficient recyclable oxidizing system Synlett. 2010: 2771-2774. DOI: 10.1055/S-0030-1259011 |
0.465 |
|
| 2010 |
Yusubov MS, Yusubova RY, Funk TV, Chi KW, Kirschning A, Zhdankin VV. M-iodosylbenzoic acid as a convenient recyclable hypervalent iodine oxidant for the synthesis of α-iodo ketones by oxidative iodination of ketones Synthesis. 3681-3685. DOI: 10.1055/S-0030-1258223 |
0.45 |
|
| 2010 |
Neu HM, Zhdankin VV, Nemykin VN. Binuclear iron(III) phthalocyanine(μ-oxodimer)/tetrabutylammonium oxone: a powerful catalytic system for oxidation of hydrocarbons in organic solution Tetrahedron Letters. 51: 6545-6548. DOI: 10.1016/J.Tetlet.2010.10.023 |
0.407 |
|
| 2010 |
Yusubov MS, Nemykin VN, Zhdankin VV. Transition metal-mediated oxidations utilizing monomeric iodosyl- and iodylarene species Tetrahedron. 66: 5745-5752. DOI: 10.1016/J.Tet.2010.04.046 |
0.419 |
|
| 2010 |
Yusubov MSo, Zhdankin VV. Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds Mendeleev Communications. 20: 185-191. DOI: 10.1016/J.Mencom.2010.06.001 |
0.434 |
|
| 2010 |
Yoshimura A, Neu H, Nemykin V, Zhdankin V. Metalloporphyrin/Iodine(III)-Cocatalyzed Oxygenation of Aromatic Hydrocarbons Advanced Synthesis & Catalysis. 352: 1455-1460. DOI: 10.1002/Adsc.201000172 |
0.406 |
|
| 2009 |
Mailyan AK, Geraskin IM, Nemykin VN, Zhdankin VV. 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. The Journal of Organic Chemistry. 74: 8444-7. PMID 19795852 DOI: 10.1021/Jo901638F |
0.433 |
|
| 2009 |
Yusubov MS, Zagulyaeva AA, Zhdankin VV. Iodine(V)/ruthenium(III)-cocatalyzed oxidations: a highly efficient tandem catalytic system for the oxidation of alcohols and hydrocarbons with oxone. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11091-4. PMID 19760738 DOI: 10.1002/Chem.200901953 |
0.389 |
|
| 2009 |
Nemykin VN, Koposov AY, Netzel BC, Yusubov MS, Zhdankin VV. Self-assembly of hydroxy(phenyl)iodonium ions in acidic aqueous solution: preparation, and X-ray crystal structures of oligomeric phenyliodine(III) sulfates. Inorganic Chemistry. 48: 4908-17. PMID 19382777 DOI: 10.1021/Ic900282K |
0.36 |
|
| 2009 |
Zhdankin VV. Hypervalent iodine(III) reagents in organic synthesis Arkivoc. 2009: 1-62. DOI: 10.3998/Ark.5550190.0010.101 |
0.437 |
|
| 2009 |
Yusubov MSo, Yusubova RY, Funk TV, Chi KW, Zhdankin VV. Oligomeric Iodosylbenzene Sulfate:A Convenient Hypervalent Iodine Reagent for Oxidationof Organic Sulfides and Alkenes Synthesis. 2009: 2505-2508. DOI: 10.1055/S-0029-1216870 |
0.496 |
|
| 2009 |
Neu H, Yusubov M, Zhdankin V, Nemykin V. Binuclear Iron(III) Phthalocyanine(μ-Oxodimer)-Catalyzed Oxygenation of Aromatic Hydrocarbons with Iodosylbenzene Sulfate and Iodosylbenzene as the Oxidants Advanced Synthesis & Catalysis. 351: 3168-3174. DOI: 10.1002/Adsc.200900705 |
0.343 |
|
| 2009 |
Geraskin IM, Pavlova O, Neu HM, Yusubov MS, Nemykin VN, Zhdankin VV. 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 Advanced Synthesis and Catalysis. 351: 733-737. DOI: 10.1002/Adsc.200800784 |
0.369 |
|
| 2008 |
Zhdankin VV, Nemykin VN, Karimov RR, Kazhkenov ZG. Preparation and X-ray crystal structure of 2-iodyl-N,N-dialkylaniline oxides: first entry into the heterocyclic system of benziodoxazole. Chemical Communications (Cambridge, England). 6131-3. PMID 19082096 DOI: 10.1039/B813163E |
0.759 |
|
| 2008 |
Zhdankin VV, Stang PJ. Chemistry of polyvalent iodine Chemical Reviews. 108: 5299-5358. PMID 18986207 DOI: 10.1021/Cr800332C |
0.458 |
|
| 2008 |
Claeys DD, Moonen K, Roman BI, Nemykin VN, Zhdankin VV, Waroquier M, Van Speybroeck V, Stevens CV. Synthesis of tricyclic phosphonopyrrolidines via IMDAF: experimental and theoretical investigation of the observed stereoselectivity. The Journal of Organic Chemistry. 73: 7921-7. PMID 18785707 DOI: 10.1021/Jo801138S |
0.391 |
|
| 2008 |
Yusubov MS, Funk TV, Chi KW, Cha EH, Kim GH, Kirschning A, Zhdankin VV. Preparation and X-ray structures of 3-[Bis(trifluoroacetoxy)iodo]benzoic acid and 3-[hydroxy(tosyloxy)iodo]benzoic acid: new recyclable hypervalent iodine reagents. The Journal of Organic Chemistry. 73: 295-7. PMID 18062703 DOI: 10.1021/Jo702112S |
0.391 |
|
| 2008 |
Geraskin IM, Luedtke MW, Neu HM, Nemykin VN, Zhdankin VV. Organic iodine(V) compounds as terminal oxidants in iron(III) phthalocyanine catalyzed oxidation of alcohols Tetrahedron Letters. 49: 7410-7412. DOI: 10.1016/J.Tetlet.2008.10.060 |
0.454 |
|
| 2007 |
Karimov RR, Kazhkenov ZG, Modjewski MJ, Peterson EM, Zhdankin VV. Preparation and reactivity of polymer-supported 2-iodylphenol ethers, an efficient recyclable oxidizing system. The Journal of Organic Chemistry. 72: 8149-51. PMID 17880245 DOI: 10.1021/Jo7015746 |
0.777 |
|
| 2007 |
Yusubov MS, Tveryakova EN, Krasnokutskaya EA, Perederyna IA, Zhdankin VV. Solvent‐Free Iodination of Arenes using Iodine–Silver Nitrate Combination Synthetic Communications. 37: 1259-1265. DOI: 10.1080/00397910701216039 |
0.373 |
|
| 2007 |
Yusubov MS, Gilmkhanova MP, Zhdankin VV, Kirschning A. m-iodosylbenzoic acid as a convenient recyclable reagent for highly efficient RuCl3-catalyzed oxidation of alcohols to carbonyl compounds Synlett. 563-566. DOI: 10.1055/S-2007-970742 |
0.396 |
|
| 2007 |
Yusubov MS, Gilmkhanova MP, Zhdankin VV, Kirschning A. Oxidation of Alcohols with RuCl3 andm-Iodobenzoic Acid Synfacts. 2007: 658-658. DOI: 10.1055/S-2007-968527 |
0.356 |
|
| 2007 |
Ladziata U, Zhdankin VV. N -(2 -iodylphenyl )acylamides- : New pentavalent iodine oxidizing reagents Synlett. 2007: 527-537. DOI: 10.1055/S-2007-967983 |
0.471 |
|
| 2007 |
Stevens CV, Meenen EV, Masschelein KGR, Eeckhout Y, Hooghe W, D’hondt B, Nemykin VN, Zhdankin VV. A copper-catalyzed domino radical cyclization route to benzospiro-indolizidinepyrrolidinones Tetrahedron Letters. 48: 7108-7111. DOI: 10.1016/J.Tetlet.2007.07.211 |
0.444 |
|
| 2007 |
Gunasekera DS, Gerold DJ, Aalderks NS, Chandra JS, Maanu CA, Kiprof P, Zhdankin VV, Reddy MVR. Practical synthesis and applications of benzoboroxoles Tetrahedron. 63: 9401-9405. DOI: 10.1016/J.Tet.2007.06.099 |
0.405 |
|
| 2007 |
Koposov AY, Netzel BC, Yusubov MS, Nemykin VN, Nazarenko AY, Zhdankin VV. Preparation and structure of oligomeric iodosylbenzene sulfate (PhIO) 3·SO3: Stable and water-soluble analog of iodosylbenzene European Journal of Organic Chemistry. 4475-4478. DOI: 10.1002/Ejoc.200700625 |
0.311 |
|
| 2006 |
Koposov AY, Karimov RR, Pronin AA, Skrupskaya T, Yusubov MS, Zhdankin VV. RuCl3-catalyzed oxidation of iodoarenes with peracetic acid: new facile preparation of iodylarenes. The Journal of Organic Chemistry. 71: 9912-4. PMID 17168623 DOI: 10.1021/Jo062073S |
0.794 |
|
| 2006 |
Ochiai M, Sueda T, Miyamoto K, Kiprof P, Zhdankin VV. trans Influences on hypervalent bonding of aryl lambda(3)-iodanes: their stabilities and isodesmic reactions of benziodoxolones and benziodazolones. Angewandte Chemie (International Ed. in English). 45: 8203-6. PMID 17096441 DOI: 10.1002/Anie.200603055 |
0.345 |
|
| 2006 |
Koposov AY, Karimov RR, Geraskin IM, Nemykin VN, Zhdankin VV. 2-iodylphenol ethers: preparation, X-ray crystal structure, and reactivity of new hypervalent iodine(V) oxidizing reagents. The Journal of Organic Chemistry. 71: 8452-8. PMID 17064019 DOI: 10.1021/Jo0614947 |
0.782 |
|
| 2006 |
Ladziata U, Willging J, Zhdankin VV. Facile preparation and reactivity of polymer-supported N-(2-Iodyl-phenyl)-acylamide, an efficient oxidizing system. Organic Letters. 8: 167-70. PMID 16381594 DOI: 10.1021/Ol052684R |
0.406 |
|
| 2006 |
Ladziata U, Zhdankin VV. Hypervalent iodine(V) reagents in organic synthesis Arkivoc. 2006. DOI: 10.3998/Ark.5550190.0007.903 |
0.385 |
|
| 2006 |
Ladziata U, Willging J, Zhdankin VV. Polymeric N-(2-Iodyl-phenyl)-acylamide Reagent for Oxidation of Alcohols Synfacts. 2006: 406-406. DOI: 10.1055/S-2006-932094 |
0.371 |
|
| 2006 |
Ladziata U, Carlson J, Zhdankin VV. Synthesis and oxidative reactivity of new chiral hypervalent iodine(V) reagents based on (S)-proline Tetrahedron Letters. 47: 6301-6304. DOI: 10.1016/J.Tetlet.2006.06.103 |
0.433 |
|
| 2006 |
Yusubov MS, Chi K, Park JY, Karimov R, Zhdankin VV. Highly efficient RuCl3-catalyzed disproportionation of (diacetoxyiodo)benzene to iodylbenzene and iodobenzene; leading to the efficient oxidation of alcohols to carbonyl compounds Tetrahedron Letters. 47: 6305-6308. DOI: 10.1016/J.Tetlet.2006.06.100 |
0.786 |
|
| 2006 |
Koposov AY, Litvinov DN, Zhdankin VV, Ferguson MJ, McDonald R, Tykwinski RR. Preparation and reductive decomposition of 2-iodoxybenzenesulfonic acid. X-ray crystal structure of 1-hydroxy-1H-1,2,3-benziodoxathiole 3,3-dioxide European Journal of Organic Chemistry. 4791-4795. DOI: 10.1002/Ejoc.200600683 |
0.391 |
|
| 2006 |
Dieltiens N, Claeys DD, Zhdankin VV, Nemykin VN, Allaert B, Verpoort F, Stevens CV. The Pyroglutamate Hydantoin Rearrangement European Journal of Organic Chemistry. 2006: 2649-2660. DOI: 10.1002/Ejoc.200600051 |
0.39 |
|
| 2005 |
Ladziata U, Koposov AY, Lo KY, Willging J, Nemykin VN, Zhdankin VV. Synthesis, structure, and chemoselective reactivity of N-(2-iodylphenyl)acylamides: hypervalent iodine reagents bearing a pseudo-six-membered ring scaffold. Angewandte Chemie (International Ed. in English). 44: 7127-31. PMID 16259023 DOI: 10.1002/Anie.200502707 |
0.377 |
|
| 2005 |
Zhdankin VV, Koposov AY, Litvinov DN, Ferguson MJ, McDonald R, Luu T, Tykwinski RR. Esters of 2-iodoxybenzoic acid: hypervalent iodine oxidizing reagents with a pseudobenziodoxole structure. The Journal of Organic Chemistry. 70: 6484-91. PMID 16050713 DOI: 10.1021/Jo051010R |
0.482 |
|
| 2005 |
Yusubov MS, Drygunova LA, Tkachev AV, Zhdankin VV. Halomethoxylation of monoterpenes using (dichloroiodo)benzene Arkivoc. 2005. DOI: 10.3998/Ark.5550190.0006.414 |
0.375 |
|
| 2005 |
Zhdankin VV. Benziodoxole-Based Hypervalent Iodine Reagents in Organic Synthesis Current Organic Synthesis. 2: 121-145. DOI: 10.2174/1570179052996982 |
0.455 |
|
| 2005 |
Koposov AY, Zhdankin VV. Selective oxidation of sulfides to sulfoxides using IBX-esters Synthesis. 22-24. DOI: 10.1055/S-2004-834873 |
0.477 |
|
| 2005 |
Koposov AY, Nemykin VN, Zhdankin VV. Intra- and intermolecular interactions in the solid state structure of 2-iodylbenzenesulfonamides: A heptacoordinated organic iodine(V) compound New Journal of Chemistry. 29: 998-1000. DOI: 10.1039/B506573A |
0.306 |
|
| 2004 |
Koposov AY, Boyarskikh VV, Zhdankin VV. Amino acid-derived iodobenzene dicarboxylates: reagents for oxidative conversion of alkenes to amino acid esters. Organic Letters. 6: 3613-5. PMID 15387561 DOI: 10.1021/Ol0484714 |
0.396 |
|
| 2004 |
Zhdankin VV, Litvinov DN, Koposov AY, Luu T, Ferguson MJ, McDonald R, Tykwinski RR. Preparation and structure of 2-iodoxybenzoate esters: soluble and stable periodinane oxidizing reagents. Chemical Communications (Cambridge, England). 106-7. PMID 14737354 DOI: 10.1039/B312961F |
0.457 |
|
| 2004 |
Zhdankin VV, Goncharenko RN, Litvinov DN, Koposov AY. Derivatives of 2-iodoxybenzenesulfonic acid: New pseudocyclic hypervalent iodine reagents Arkivoc. 2005: 8-18. DOI: 10.3998/Ark.5550190.0006.402 |
0.477 |
|
| 2004 |
Yusubov MS, Drygunova LA, Zhdankin VV. 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. DOI: 10.1055/S-2004-831175 |
0.451 |
|
| 2004 |
Koposov AY, Litvinov DN, Zhdankin VV. 2-Iodoxybenzenesulfamides: New pseudobenziodoxole-based hypervalent iodine reagents Tetrahedron Letters. 45: 2719-2721. DOI: 10.1016/J.Tetlet.2004.02.053 |
0.46 |
|
| 2003 |
Zhdankin VV, Koposov AY, Su L, Boyarskikh VV, Netzel BC, Young VG. Synthesis and structure of amino acid-derived benziodazoles: new hypervalent iodine heterocycles. Organic Letters. 5: 1583-6. PMID 12713329 DOI: 10.1021/Ol0344523 |
0.462 |
|
| 2003 |
Zhdankin VV, Maydanovych O, Herschbach J, Bruno J, Matveeva ED, Zefirov NS. Preparation and chemistry of phosphoranyl-derived iodanes. The Journal of Organic Chemistry. 68: 1018-23. PMID 12558430 DOI: 10.1021/Jo026604Y |
0.458 |
|
| 2003 |
Matveeva ED, Podrugina TA, Grishin YK, Tkachev VV, Zhdankin VV, Aldoshin SM, Zefirov NS. Synthesis and Structure of Mixed Phosphonium-iodonium Ylide Russian Journal of Organic Chemistry. 39: 536-541. DOI: 10.1023/A:1026011902365 |
0.317 |
|
| 2003 |
Zhdankin VV. C-C-Bond Forming Reactions Topics in Current Chemistry. 224: 99-136. DOI: 10.1007/3-540-46114-0_4 |
0.437 |
|
| 2002 |
Zhdankin VV, Maydanovych O, Herschbach J, McDonald R, Tykwinski RR. Preparation, structure, and unexpected chemistry of phosphoranyl-derived benziodoxoles. Journal of the American Chemical Society. 124: 11614-5. PMID 12296724 DOI: 10.1021/Ja0277780 |
0.423 |
|
| 2002 |
Zhdankin VV, Stang PJ. Recent developments in the chemistry of polyvalent iodine compounds Chemical Reviews. 102: 2523-2584. PMID 12105935 DOI: 10.1021/Cr010003+ |
0.318 |
|
| 2002 |
Pirkuliyev NS, Brel VK, Zhdankin VV, Zefirov NS. Reaction of Fluoro[trifluoromethanesulfonyloxy-λ3-iodanil]benzene with Nitrogen-containing Heterocycles Russian Journal of Organic Chemistry. 38: 1224-1225. DOI: 10.1023/A:1020990618707 |
0.411 |
|
| 2002 |
Zhdankin VV, Koposov AY, Yashin NV. Complexes of hypervalent iodine compounds with nitrogen ligands Tetrahedron Letters. 43: 5735-5737. DOI: 10.1016/S0040-4039(02)01192-9 |
0.341 |
|
| 2002 |
Zhdankin VV, Maydanovych O, Herschbach J, Bruno J, Matveeva ED, Zefirov NS. Preparation, structure, and chemistry of phosphorane-derived phenyliodonium sulfonates Tetrahedron Letters. 43: 2359-2361. DOI: 10.1016/S0040-4039(02)00275-7 |
0.432 |
|
| 2001 |
Zhdankin VV, Koposov AE, Smart JT, Tykwinski RR, McDonald R, Morales-Izquierdo A. Secondary bonding-directed self-assembly of amino acid derived benziodazoles: synthesis and structure of novel hypervalent iodine macrocycles. Journal of the American Chemical Society. 123: 4095-6. PMID 11457167 DOI: 10.1021/Ja0155276 |
0.318 |
|
| 2000 |
Zhdankin VV, Persichini PJ, Cui R, Jin Y. A Convenient Synthesis of Alkynyliodonium Salts from Alkynylboronates and Hypervalent Iodine Reagents Synlett. 2000: 719-721. DOI: 10.1055/S-2000-6627 |
0.397 |
|
| 2000 |
Zhdankin VV, Smart JT, Zhao P, Kiprof P. Synthesis and reactions of amino acid-derived benziodazole oxides: new chiral oxidizing reagents Tetrahedron Letters. 41: 5299-5302. DOI: 10.1016/S0040-4039(00)00836-4 |
0.441 |
|
| 1999 |
Magerramov AM, Allakhverdiev AM, Akhmedova ZI, Caple R, Zhdankin VV. New Synthesis of Tetrahydro-L,4-Thiazine-3-Ones from 1,2-Aminopropanethiols and α-Chlorocarboxylic Acids Synthetic Communications. 29: 721-728. DOI: 10.1080/00397919908085822 |
0.306 |
|
| 1999 |
Zhdankin VV. Chemistry of Hypervalent Compounds Edited by Kin-ya Akiba (Hiroshima University). Wiley-VCH: New York. 1998. xvi + 414 pp. $135.00. ISBN 0-471-24019-2. Journal of the American Chemical Society. 121: 6971-6971. DOI: 10.1021/Ja995694U |
0.323 |
|
| 1999 |
Zhdankin VV, Persichini PJ, Zhang L, Fix S, Kiprof P. Synthesis and structure of benzoboroxoles: Novel organoboron heterocycles Tetrahedron Letters. 40: 6705-6708. DOI: 10.1016/S0040-4039(99)01303-9 |
0.381 |
|
| 1999 |
Zhdankin VV, Callies JA, Hanson KJ, Bruno J. New alkyliodonium derivatives stabilized by ammonium or phosphonium groups Tetrahedron Letters. 40: 1839-1842. DOI: 10.1016/S0040-4039(99)00082-9 |
0.314 |
|
| 1998 |
Zhdankin VV, Arbit RM, Lynch BJ, Kiprof P, Young VG. Structure and Chemistry of Hypervalent Iodine Heterocycles: Acid-Catalyzed Rearrangement of Benziodazol-3-ones to 3-Iminiumbenziodoxoles Journal of Organic Chemistry. 63: 6590-6596. DOI: 10.1021/Jo980745B |
0.436 |
|
| 1998 |
Zhdankin VV, Stang PJ. Alkynyliodonium salts in organic synthesis Tetrahedron. 54: 10927-10966. DOI: 10.1016/S0040-4020(98)00410-4 |
0.322 |
|
| 1997 |
Zhdankin VV, Arbit RM, McSherry M, Mismash B, Young VG. Structure and chemistry of acetoxybenziodazole. Acid-catalyzed rearrangement of benziodazoles to 3-iminobenziodoxoles Journal of the American Chemical Society. 119: 7408-7409. DOI: 10.1021/Ja971606Z |
0.347 |
|
| 1997 |
Zhdankin VV, Erickson SA, Hanson KJ. Preparation, X-ray crystal structure, and chemistry of ((arylsulfonyl)methyl)(phenyl)iodonium triflates. Stable aikyliodonium salts Journal of the American Chemical Society. 119: 4775-4776. DOI: 10.1021/Ja9707926 |
0.329 |
|
| 1997 |
Papoutsis I, Spyroudis S, Varvoglis A, Callies JA, Zhdankin VV. Novel trifluoroethyliodonium salts from cyclic enaminones and their thermal decomposition Tetrahedron Letters. 38: 8401-8404. DOI: 10.1016/S0040-4039(97)10232-5 |
0.403 |
|
| 1997 |
Zhdankin VV, McSherry M, Mismash B, Bolz JT, Woodward JK, Arbit RM, Erickson S. 1-Amido-3-(1H)-1,2-benziodoxoles: Stable amidoiodanes and reagents for direct amidation of organic substrates Tetrahedron Letters. 38: 21-24. DOI: 10.1016/S0040-4039(96)02245-9 |
0.364 |
|
| 1996 |
Zhdankin VV, Kuehl CJ, Simonsen AJ. 1-[Hydroxy(sulfonyloxy)iodo]-1H,1H-perfluoroalkanes: Stable, Fluoroalkyl Analogs of Koser's Reagent. The Journal of Organic Chemistry. 61: 8272-8276. PMID 11667815 DOI: 10.1021/Jo961336N |
0.332 |
|
| 1996 |
Zhdankin VV, Kuehl CJ, Krasutsky AP, Bolz JT, Simonsen AJ. 1-(Organosulfonyloxy)-3(1H)-1,2-benziodoxoles: Preparation and Reactions with Alkynyltrimethylsilanes. The Journal of Organic Chemistry. 61: 6547-6551. PMID 11667518 DOI: 10.1021/Jo960927A |
0.393 |
|
| 1996 |
Zhdankin VV, Kuehl CJ, Simonsen AJ. Iodosylperfluoroalkanes as Reagents for the Preparation of Perfluoroalkyliodonium Salts under Aprotic Conditions Main Group Chemistry. 1: 349-352. DOI: 10.1080/13583149612331338657 |
0.414 |
|
| 1996 |
Zhdankin VV, Kuehl CJ, Arif AM, Stang PJ. Synthesis and X-ray crystal structure of l-cyano-3,3-bis(trifluoromethyl)-l,3-dihydro-lλ3,2-benzoiodoxole, a stable cyanoiodolane Mendeleev Communications. 6: 50-51. DOI: 10.1070/Mc1996V006N02Abeh000575 |
0.336 |
|
| 1996 |
Zhdankin VV, Krasutsky AP, Kuehl CJ, Simonsen AJ, Woodward JK, Mismash B, Bolz JT. Preparation, X-ray Crystal Structure, and Chemistry of Stable AzidoiodinanesDerivatives of Benziodoxole Journal of the American Chemical Society. 118: 5192-5197. DOI: 10.1021/Ja954119X |
0.361 |
|
| 1995 |
Kuehl CJ, Bolz JT, Zhdankin VV. (Hydroxy(sulfonyloxy)iodo)perfluoroalkanes: New and Convenient Reagents for the Preparation of Fluoroalkyl(aryl)iodonium Salts. Synthesis. 1995: 312-316. DOI: 10.1055/S-1995-4428 |
0.419 |
|
| 1995 |
Zhdankin VV, Kuehl CJ, Simonsen AJ. 1-[Hydroxy(sulfonyloxy)iodo]-2,2,2-trifluoroethanes, CF3CH2I(OH)OSO2R: Stable, fluoroalkyl analogs of Koser's reagent Tetrahedron Letters. 36: 2203-2206. DOI: 10.1016/0040-4039(95)00275-H |
0.439 |
|
| 1994 |
Zhdankin VV, Kuehl CJ, Bolz JT, Zefirov NS. A General Synthetic Approach to Aryl(perfluoroalkyl)iodonium Sulfonates by the Reaction of [Hydroxy(sulfonyloxy)iodo]perfluoroalkanes with Arylsilanes Mendeleev Communications. 4: 165-166. DOI: 10.1070/Mc1994V004N05Abeh000395 |
0.392 |
|
| 1994 |
Zhdankin VV, Kuehl C. [Hydroxy(sulfonyloxy)iodo]perfluoroalkanes - new hypervalent iodine species and promising reagents for organic synthesis Tetrahedron Letters. 35: 1809-1812. DOI: 10.1016/S0040-4039(00)73166-2 |
0.434 |
|
| 1994 |
Zhdankin VV, Kuehl CJ, Krasutsky AP, Formaneck MS, Bolz JT. Preparation and chemistry of stable azidoiodinanes: 1-Azido-3,3-bis(trifluoromethyl)-3-(1H)-1,2-benziodoxol and 1-Azido-1,2-benziodoxol-3-(1H)-one Tetrahedron Letters. 35: 9677-9680. DOI: 10.1016/0040-4039(94)88357-2 |
0.409 |
|
| 1994 |
Zhdankin VV, Kuehl CJ, Bolz JT, Formaneck MS, Simonsen AJ. 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 Letters. 35: 7323-7326. DOI: 10.1016/0040-4039(94)85304-5 |
0.388 |
|
| 1993 |
Zefirov NS, Kasumov TM, Koz'min AS, Sorokin VD, Stang PJ, Zhdankin VV. Iodosyl fluorosulfate - A new efficient reagent for the direct synthesis of diaryliodonium salts Synthesis. 1993: 1209-1210. DOI: 10.1055/S-1993-26024 |
0.415 |
|
| 1993 |
Stang PJ, Blume T, Zhdankin VV. Synthesis of enediynes by reaction of bicycloalkenyldiiodonium salts with lithium alkynylcuprates Synthesis. 1993: 35-36. DOI: 10.1055/S-1993-25783 |
0.38 |
|
| 1993 |
Gallop PM, Paz MA, Fluckiger R, Stang PJ, Zhdankin VV, Tykwinski RR. Highly effective PQQ inhibition by alkynyl and aryl mono- and diiodonium salts Journal of the American Chemical Society. 115: 11702-11704. DOI: 10.1021/Ja00078A007 |
0.329 |
|
| 1993 |
Stang PJ, Zhdankin VV. Preparation and characterization of a macrocyclic tetraaryltetraiodonium compound, cyclo(Ar4I4)4+.cntdot.4X-. A unique, charged, cationic molecular box Journal of the American Chemical Society. 115: 9808-9809. DOI: 10.1021/Ja00074A061 |
0.305 |
|
| 1993 |
Zhdankin VV, Scheuller MC, Stang PJ. A general approach to aryl(cyano)iodonium triflates - versatile iodonium transfer reagents Tetrahedron Letters. 34: 6853-6856. DOI: 10.1016/S0040-4039(00)91812-4 |
0.461 |
|
| 1992 |
Stang PJ, Zhdankin VV, Arif AM. Synthesis and X-Ray Structure Determination of 1,4-Bis[trimethylsilylethynyl(trifluoromethanesulfonyloxy)iodo]benzene, Me3SiCCl+C6H4l+CCSiMe3 2CF3SO3−, a Novel Alkynyliodonium Salt Mendeleev Communications. 2: 158-159. DOI: 10.1070/Mc1992V002N04Abeh000184 |
0.391 |
|
| 1992 |
Zhdankin VV, Stang PJ, Zefirov NS. Preparation, spectral identification and chemical reaction of alkynyl xenonium tetrafluoroborates, R-C≡C-Xe+ BF4 -: Novel organoxenonium species Journal of the Chemical Society, Chemical Communications. 578-579. DOI: 10.1039/C39920000578 |
0.352 |
|
| 1992 |
Zefirov NS, Koz'min AS, Kasumov T, Potekhin KA, Sorokin VD, Brel VK, Abramkin EV, Struchkov YT, Zhdankin VV, Stang PJ. Interaction of an allene with polyvalent iodine derivatives. Preparation, X-ray molecular structure, and some reactions of phenyl(2,2-dimethyl-4-(diethylphosphono)-2,5-dihydro-3-furyl)iodonium salts Journal of Organic Chemistry. 57: 2433-2437. DOI: 10.1021/Jo00034A043 |
0.339 |
|
| 1992 |
Stang PJ, Tykwinski R, Zhdankin VV. Bis(phenyliodonium) diyne triflates PhIC.tplbond.C(p-C6H4)nC.tplbond.CIPh.cntdot.20Tf and PhIC.tplbond.C(CH2)nC.tplbond.CIPh.cntdot.20Tf: preparation, characterization, and reaction with triphenylphosphine The Journal of Organic Chemistry. 57: 1861-1864. DOI: 10.1021/Jo00032A046 |
0.372 |
|
| 1992 |
Stang PJ, Zhdankin VV, Tykwinski R, Zefirov NS. (Dicyano)iodonium triflate- novel iodonium species and a versatile reagent for the preparation of iodonium salts via an iodonium transfer reaction with organostannanes Tetrahedron Letters. 33: 1419-1422. DOI: 10.1016/S0040-4039(00)91636-8 |
0.421 |
|
| 1992 |
Stang PJ, Schwarz A, Blume T, Zhdankin VV. Reactions of bicycloalkenyldiiodonium salts with nucleophiles Tetrahedron Letters. 33: 6759-6762. DOI: 10.1016/S0040-4039(00)61769-0 |
0.398 |
|
| 1992 |
Stang PJ, Tykwinski R, Zhdankin VV. Preparation of bis(heteroaryl)iodonium saltsviaan iodonium transfer reaction between di(cyano)iodonium triflate and organostannes Journal of Heterocyclic Chemistry. 29: 815-818. DOI: 10.1002/Jhet.5570290424 |
0.414 |
|
| 1991 |
Zefirov NS, Gakh AA, Zhdankin VV, Stang PJ. Interaction of fluoroxenonium triflate, fluorosulfate and nitrate with alkenes. Stereochemical evidence for the electrophilic noble gas cation addition to the carbon-carbon double bond Journal of Organic Chemistry. 56: 1416-1418. DOI: 10.1021/Jo00004A015 |
0.388 |
|
| 1991 |
Stang PJ, Zhdankin VV. Preparation and Chemistry of PhI+C≡CI+Ph·2-OTf, Bis[phenyl[[(trifluoromethyl)sulfonyl]oxy]iodo]acetylene, a Novel Difunctional Acetylene, Bis(iodonium) Species and a Stable C2-Transfer Agent Journal of the American Chemical Society. 113: 4571-4576. DOI: 10.1021/Ja00012A028 |
0.412 |
|
| 1991 |
Zhdankin VV, Tykwinski R, Williamson BL, Stang PJ, Zefirov NS. (Dicyanoiodo)benzene - a stable tricoordinate iodine(III) compound with three carbon ligands Tetrahedron Letters. 32: 733-734. DOI: 10.1016/S0040-4039(00)74870-2 |
0.347 |
|
| 1991 |
Stang PJ, Arif AM, Zhdankin VV. Reaction OF E-1,2-bis[triphenyl(trifluoromethanesulfonyloxy)phospho]ethylene, Ph3PCHCHPPh3·20Tfwith bases: Unusual products and evidence for C2-dlylide, Ph3PCCPPh3, formation Tetrahedron. 47: 4539-4546. DOI: 10.1016/S0040-4020(01)86460-7 |
0.337 |
|
| 1991 |
Stang PJ, Zhdankin VV, Tykwinski R, Zefirov NS. Iodosyl trifluoromethanesulfonate - an efficient reagent for the single step preparation of diaryl iodonium triflate salts Tetrahedron Letters. 32: 7497-7498. DOI: 10.1016/0040-4039(91)80516-9 |
0.424 |
|
| 1990 |
Brel VK, Koz'min AS, Uvarov VI, Zefirov NS, Zhdankin VV, Stang PJ. Xenon fluorosulfates and their AdE-reactions with olefins Tetrahedron Letters. 31: 5225-5226. DOI: 10.1016/S0040-4039(00)97849-3 |
0.328 |
|
| 1990 |
Zhdankin VV, Crittell CM, Stang PJ, Zefirov NS. A general approach to unsymmetrical tricoordinate iodinanes: Single step preparation of mixed iodosobenzene sulfonates Phl(X)OSO2R, via reaction of iodosobenzene with Me3SiX Tetrahedron Letters. 31: 4821-4824. DOI: 10.1016/S0040-4039(00)97741-4 |
0.359 |
|
| 1990 |
Brel VK, Koz'min AS, Martynov IV, Uvarov VI, Zefirov NS, Zhdankin VV, Stang PJ. Introduction of the halonitromethyl framework into aromatic rings via a XeF2 mediated radical process Tetrahedron Letters. 31: 4799-4800. DOI: 10.1016/S0040-4039(00)97737-2 |
0.35 |
|
| 1990 |
Trushkov IV, Zhdankin VV, Koz'min AS, Zefirov NS. Cubic reaction coordinate diagram in the nucleophilic substitution process Tetrahedron Letters. 31: 3199-3200. DOI: 10.1016/S0040-4039(00)94731-2 |
0.348 |
|
| 1989 |
Zhdankin VV, Mullikin M, Tykwinski R, Berglund B, Caple R, Zefirov NS, Koz'min AS. Carbon-carbon bond formation in reactions of PhIO.cntdot.HBF4-silyl enol ether adduct with alkenes or silyl enol ethers The Journal of Organic Chemistry. 54: 2605-2608. DOI: 10.1021/Jo00272A028 |
0.327 |
|
| 1988 |
Zefirov NS, Zhdankin VV, Koz'min AS. The Synthesis and Properties of Covalent Organic Perchlorates Russian Chemical Reviews. 57: 1041-1053. DOI: 10.1070/Rc1988V057N11Abeh003410 |
0.37 |
|
| 1988 |
Zhdankin VV, Tykwinski R, Caple R, Berglund B, Koz'min AS, Zefirov NS. Iodosobenzene tetrafluoroborate: First example of a stable electrophilic hypervalent iodine reagent without nucleophilic ligands Tetrahedron Letters. 29: 3717-3720. DOI: 10.1016/S0040-4039(00)82162-0 |
0.415 |
|
| 1988 |
Zhdankin VV, Tykwinski R, Caple R, Berglund B, Koz'min AS, Zefirov NS. Reaction of phIO·HBF4/silyl enol ether adduct with olefins as general approach to carbon—carbon bond formation in AdE reactions using hypervalent iodine reagents Tetrahedron Letters. 29: 3703-3704. DOI: 10.1016/S0040-4039(00)82158-9 |
0.362 |
|
| 1988 |
Zefirov NS, Zhdankin VV, Koz'min AS, Fainzilberg AA, Gakh AA, Ugrak BI, Romaniko SV. Cesium fluoroxysulfate addition to alkenes leading to vicinal fluoroalkylsulfates Tetrahedron. 44: 6505-6513. DOI: 10.1016/S0040-4020(01)89839-2 |
0.36 |
|
| 1988 |
Zefirov NS, Caple R, Palyulin VA, Berglund B, Tykvinskii R, Zhdankin V, Koz'min AS. Ring contraction in the reaction of cyclic olefins with iodine(III)-containing reagents Russian Chemical Bulletin. 37: 1289-1289. DOI: 10.1007/Bf00961969 |
0.402 |
|
| 1987 |
Zefirov NS, Zhdankin VV, Gakh AA, Ugrak BI, Roroaniko SV, Koz'min AS, Fainzil'berg AA. Fluorosulfation of the double bond: A new direction in the reactions of cesium fluoroxysulfate with olefins Russian Chemical Bulletin. 36: 2451-2451. DOI: 10.1007/Bf00957353 |
0.35 |
|
| 1987 |
Zefirov NS, Zhdankin VV, Koz'min AS, Semerikov VN, Agaev AT, Magerramov AM. Formation of a carbon-carbon bond in the reactions of olefins with iodonium ylids under lewis acid catalysis conditions Russian Chemical Bulletin. 36: 2672-2672. DOI: 10.1007/Bf00957274 |
0.321 |
|
| 1986 |
Zefirov NS, Zhdankin VV, Dan'kov YV, Sorokin VD, Semerikov VN, Koz'min AS, Caple R, Berglund BA. Novel reagents containing hypervalent iodine and their use for electrophilic additions to olefins Tetrahedron Letters. 27: 3971-3974. DOI: 10.1016/S0040-4039(00)84887-X |
0.452 |
|
| 1986 |
Zefirov NS, Zhdankin VV, Koz'min AS. Stereochemistry of oxidative deiodination leading to formation of covalent perchlorates Tetrahedron Letters. 27: 1845-1846. DOI: 10.1016/S0040-4039(00)84391-9 |
0.387 |
|
| 1986 |
Zefirov NS, Koz'min AS, Sorokin VD, Zhdankin VV. Activation of the Electrophilic Reactivities of Chlorine and of Alkyl Hypochlorites by Sulphonates Obtained by Insertion of Sulphur Trioxide in the Cl - Cl and O - Cl Bonds. Addition of Chloro- and Ethoxysulphonyloxy Chloride to Alken Cheminform. 17. DOI: 10.1002/Chin.198637090 |
0.313 |
|
| 1986 |
Zefirov NS, Sorokin VD, Zhdankin VV, Koz'min AS. Sulphates of Trivalent Iodine. Novel Reagents for the Functionalization of Olefins to Cyclic Sulphates. Cheminform. 17. DOI: 10.1002/Chin.198624198 |
0.424 |
|
| 1986 |
Zefirov NS, Zhdankin VV, Dan'kov YV, Koz'min AS, Chizhov OS. Phenyliodo(III)hydroxymesylate - a Novel Reagent for the Oxymesylation of Ketones and Olefines. Cheminform. 17. DOI: 10.1002/Chin.198611150 |
0.368 |
|
| 1985 |
Zefirov NS, Zhdankin VV, Sorokin VD, Koz'min AS. Novel Method of Deoxidation of Alcohols and Its Use in Synthesis of Covalent Perchlorates. Tetrahedron Letters. 26: 6243-6244. DOI: 10.1016/S0040-4039(00)95063-9 |
0.319 |
|
| 1985 |
Zefirov NS, Koz'min AS, Sorokin VD, Zhdankin VV, Studnev YN, Fokin AV. Competitive Binding Of Fluorosulfate Anion In Reactions Of Halogens And Nitronium Borofluoride With Olefins Russian Chemical Bulletin. 34: 356-358. DOI: 10.1007/Bf00951286 |
0.385 |
|
| 1985 |
Zefirov NS, Zhdankin VV, Makhon'kova GV, Dan'kov YV, Koz'min AS. Oxidatively Assisted Nucleophilic Substitution Of Iodine In Alkyl Iodides By Nucleofugic Anions Cheminform. 16. DOI: 10.1002/Chin.198543092 |
0.457 |
|
| 1984 |
Zefirov NS, Zhdankin VV, Dan'kov YV, Koz'min AS. Aryliodoso Derivatives As Reagents For The Functioning Of Olefins Into Vicinal Diesters Of Trifluoromethanesulfonic And Perchloric Acids Cheminform. 15. DOI: 10.1002/Chin.198425118 |
0.324 |
|
| 1984 |
ZEFIROV NS, ZHDANKIN VV, DAN'KOV YV, SAMOSHIN VV, KOZ'MIN AS. ChemInform Abstract: COMPETITIVE BINDING OF PERCHLORATE AND TRIFLUOROMETHANESULFONATE ANIONS IN REACTIONS OF ARYLIODOSO DERIVATIVES WITH OLEFINS Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198425117 |
0.359 |
|
| 1984 |
Zefirov NS, Zhdankin VV, Koz'min AS. Reaction Of Alkyl Iodides With Aryliodoso Derivatives Cheminform. 15. DOI: 10.1002/Chin.198405093 |
0.408 |
|
| 1983 |
Zefirov NS, Zhdankin VV, Kozmin AS. Reaction of alkyl iodides with aryliodoso derivatives Russian Chemical Bulletin. 32: 1530-1531. DOI: 10.1007/Bf00954382 |
0.408 |
|
| 1983 |
Zefirov NS, Koz'min AS, Yur'eva NM, Zhdankin VV, Kirin VN. A new reaction of α-epoxides: Ring opening with the formation of nitratoperchlorates Russian Chemical Bulletin. 32: 642-642. DOI: 10.1007/Bf00953133 |
0.364 |
|
| 1983 |
Zefirov NS, Koz'min AS, Sorokin VD, Zhdankin VV. Participation Of Trifluoromethanesulfonate And Fluorosulfonate Anions In The Addition Of 2‐Nitrophenylsulfenyl Chloride To Dimethyl Ester Of Tricyclo(4.2.2.02,5)Deca‐3,7,9‐Triene‐9,10‐Dicarboxylic Acid Cheminform. 14. DOI: 10.1002/Chin.198336180 |
0.336 |
|
| 1983 |
Zefirov NS, Koz'min AS, Kirin VN, Yur'eva NM, Zhdankin VV. Formation Of Alkyl Perchlorates In The Deamination Of Alkylamines In The Presence Of Perchlorate Anion Sources Cheminform. 14. DOI: 10.1002/Chin.198321142 |
0.308 |
|
| 1983 |
Zefirov NS, Koz'min AS, Zhdankin VV, Nikulin AV, Zyk NV. Lithium Perchlorate As A Reagent For Synthesis Of Covalently Bonded Organic Perchlorates Via Electrophilic Additions Of Halogens And Nitronium Fluoroborate To Olefins Cheminform. 14. DOI: 10.1002/Chin.198314170 |
0.357 |
|
| 1983 |
Zefirov NS, Koz'min AS, Yur'eva NM, Zhdankin VV, Kirin VN. Formation Of Covalent Perchlorates In The Acid Cleavage Of A Tricyclo(4.2.2.02,5)Decane Epoxide In The Presence Of Lithium Perchlorate Cheminform. 14. DOI: 10.1002/Chin.198308149 |
0.34 |
|
| 1983 |
Zefirov NS, Koz'min AS, Dan'kov YV, Zhdankin VV, Kirin VN. Tosylate And Mesylate Anions As Nucleophiles In The Conjugated Electrophilic Addition Of Halogens To Olefins Cheminform. 14. DOI: 10.1002/Chin.198301191 |
0.42 |
|
| 1982 |
Zefirov NS, Koz'min AS, Zhdankin V, Nikulin AV, Zyk NV. Lithium Perchlorate as a Reagent for Synthesis of Covalently Bonded Organic Perchlorates via Electrophilic Additions of Halogens and Nitronium Tetrafluoroborate to Olefins Journal of Organic Chemistry. 47: 3679-3684. DOI: 10.1021/Jo00140A018 |
0.357 |
|
| 1982 |
Zefirov NS, Koz'min AS, Kirin VN, Yur'eva NM, Zhdankin VV. Formation of alkyl perchlorates in the deamination of alkylamines in the presence of perchlorate anion sources Russian Chemical Bulletin. 31: 2330-2330. DOI: 10.1007/Bf00958437 |
0.308 |
|
| 1982 |
Zefirov NS, Zhdankin VV, Koz'min AS. Competing binding of perchlorate anion in oxidative elimination of iodine reactions Russian Chemical Bulletin. 31: 1497-1497. DOI: 10.1007/Bf00954202 |
0.406 |
|
| 1982 |
Zefirov NS, Koz'min AS, Sorokin VD, Zhdankin VV. Nucleophilic Properties Of Trifluoromethanesulfonate-Anion In Conjugated Ade-Reactions - Synthesis Of Beta-Halogenalkyltriflats Zhurnal Organicheskoi Khimii. 13: 1768-1769. DOI: 10.1002/Chin.198249162 |
0.332 |
|
| 1982 |
Zefirov NS, Koz'min AS, Zhdankin VV. Participation Of The Perchlorate Anion In Addition Reactions Of Arylthio Chlorides And Halogens With Unsaturated Derivatives Of Tricyclo(4.2.2.02,5)Decane. Synthesis Of Stable Covalent Perchlorates Cheminform. 13. DOI: 10.1002/Chin.198227159 |
0.443 |
|
| 1981 |
Zefirov NS, Zhdankin VV, Nikulin AV, Zyk NV, Koz'min AS. New Reaction Of Conjugated Electrophilic Addition: Functionalization Of Olefins With The Formation Of Nitroperchlorates Cheminform. 12. DOI: 10.1002/Chin.198118111 |
0.391 |
|
| 1980 |
Zefirov NS, Koz'min AS, Zhdankin VV, Kirin VN, Sergeev GB. New Electrophilic Coperchloration Of Olefins Cheminform. 11. DOI: 10.1002/Chin.198035132 |
0.304 |
|
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