about
The IX (X=O,N,C) Double Bond in Hypervalent Iodine Compounds: Is it Real?IBX amides: a new family of hypervalent iodine reagents.Preparation and X-ray crystal study of benziodoxaborole derivatives: new hypervalent iodine heterocycles.Facile One-Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone.Advances in Synthetic Applications of Hypervalent Iodine Compounds.Synthetic applications of pseudocyclic hypervalent iodine compounds.Hofmann rearrangement of carboxamides mediated by hypervalent iodine species generated in situ from iodobenzene and oxone: reaction scope and limitations.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.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.Preparation and chemistry of phosphoranyl-derived iodanes.Preparation and X-ray crystal structure of 2-iodyl-N,N-dialkylaniline oxides: first entry into the heterocyclic system of benziodoxazole.Esters of 2-iodoxybenzoic acid: hypervalent iodine oxidizing reagents with a pseudobenziodoxole structure.Preparation and X-ray structures of 3-[Bis(trifluoroacetoxy)iodo]benzoic acid and 3-[hydroxy(tosyloxy)iodo]benzoic acid: new recyclable hypervalent iodine reagents.Synthesis of tricyclic phosphonopyrrolidines via IMDAF: experimental and theoretical investigation of the observed stereoselectivity.Pseudocyclic Arylbenziodoxaboroles: Efficient Benzyne Precursors Triggered by Water at Room Temperature.Hypervalent Iodine Reagent Mediated Oxidative Heterocyclization of Aldoximes with Heterocyclic Alkenes.Preparation, Structure, and Reactivity of Pseudocyclic Benziodoxole Tosylates: New Hypervalent Iodine Oxidants and Electrophiles.Editorial for the Special Issue on Hypervalent Iodine Reagents.Secondary bonding-directed self-assembly of amino acid derived benziodazoles: synthesis and structure of novel hypervalent iodine macrocycles.Iodine(III)-Catalyzed Formal [2 + 2 + 1] Cycloaddition Reaction for Metal-Free Construction of Oxazoles.Tetra-n-butylammonium Iodide Catalyzed C-H Azidation of Aldehydes with Thermally Stable Azidobenziodoxolone.2-Iodoxybenzoic acid organosulfonates: preparation, X-ray structure and reactivity of new, powerful hypervalent iodine(V) oxidants.Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents.One-pot synthesis of diaryliodonium salts from arenes and aryl iodides with Oxone-sulfuric acid.Preparation, structure, and reactivity of bicyclic benziodazole: a new hypervalent iodine heterocycle.Synthesis of Five-Membered Iodine-Nitrogen Heterocycles from Benzimidazole-Based Iodonium SaltsOrganic Polyvalent Iodine CompoundsPreparation and X-ray structure of 2-iodoxybenzenesulfonic acid (IBS) - a powerful hypervalent iodine(V) oxidantIodonium Salts as Benzyne Precursors.Synthesis and structure of amino acid-derived benziodazoles: new hypervalent iodine heterocycles1-(Organosulfonyloxy)-3(1H)-1,2-benziodoxoles: Preparation and Reactions with Alkynyltrimethylsilanes1-[Hydroxy(sulfonyloxy)iodo]-1H,1H-perfluoroalkanes: Stable, Fluoroalkyl Analogs of Koser's ReagentPreparation and structure of 2-iodoxybenzoate esters: soluble and stable periodinane oxidizing reagentsPreparation, structure, and unexpected chemistry of phosphoranyl-derived benziodoxoles2-iodylphenol ethers: preparation, X-ray crystal structure, and reactivity of new hypervalent iodine(V) oxidizing reagentstrans Influences on hypervalent bonding of aryl lambda(3)-iodanes: their stabilities and isodesmic reactions of benziodoxolones and benziodazolonesRuCl3-catalyzed oxidation of iodoarenes with peracetic acid: new facile preparation of iodylarenesAmino acid-derived iodobenzene dicarboxylates: reagents for oxidative conversion of alkenes to amino acid estersPreparation and reactivity of polymer-supported 2-iodylphenol ethers, an efficient recyclable oxidizing systemSynthesis, structure, and chemoselective reactivity of N-(2-iodylphenyl)acylamides: hypervalent iodine reagents bearing a pseudo-six-membered ring scaffold
P50
Q30052081-184DCD88-4ED6-4A71-A758-D6E5623A31E2Q30796107-B1D8ECC9-DCF1-4993-98CC-9ED568F36E2EQ34046171-F010A0FD-E69B-47D2-92DC-7A99B6203770Q37620600-81DEAB97-C9C7-4603-8BC6-E7BE6D3F5EB6Q38727919-52D7592D-B580-43A2-BC64-D28B5918271AQ38824952-402E313B-87E1-4034-ADDE-BBE6C62CE45CQ42906778-0BE103EE-BE49-48F7-AFE6-96A0EBEFAD10Q43159341-13D1B814-6F30-4CD9-806C-7F684C9318ACQ43268685-DFDA1798-D239-400B-ACD7-EE1850C6B392Q44296817-C8FE70C8-D97C-4973-99DD-881D0DEF6AF6Q46198678-B8641ED4-7106-4FCC-8D11-0E8D2ACFCCBBQ46623620-A2C44F10-E036-4C9E-8DDE-4CAF26AA8A6BQ46863749-ECAF6775-D9D6-4C9D-9B77-D497D0E09DDFQ47351995-8EFF0FD0-DCC9-4CC3-87D0-4CB5D0AE1BE7Q47598585-26E80187-426E-407E-B287-CF91C72E70BFQ48088965-DC427618-3316-432E-803F-3B2171611573Q48266771-7445031E-501A-4949-BD4A-CF33946C376FQ48283819-1FEB8E5A-D357-46AD-9382-8C874BDD8619Q49320952-C6198B43-1F83-43C4-9784-FF725F70B8C2Q50889520-C472BB98-60E3-47F9-AD16-8AA02C3EB9E6Q51676007-79355F9C-5A06-4697-B1B3-6756744B7913Q54705501-110A3374-C6D4-4F6A-9E63-D09A60EDDA7CQ55155664-48C4C7AE-2104-4745-AA29-91934C68D70DQ55322515-BE55C9DD-86DC-4DC2-A2C9-EA9F26C0C158Q55425968-A6C3B000-1303-475C-A5E4-C3B54E5D2091Q56983197-97651F0C-D003-47E3-AE1A-C0454CC9DBB6Q60326428-0AE3D508-877F-41B0-81F9-F2F77451519CQ60368538-8FF3C381-643B-46D0-86C0-19EEE7AFBBADQ64976238-B6C7BAB8-7621-4FE8-B458-37157A67C83AQ73313963-BFEA9C54-21BB-4B9C-9A91-101B7B16FD30Q74824044-94ACF03E-420C-40DD-AD6A-F09B69F41355Q74824863-8F70A559-B987-4DAD-84E0-860AC25A0C51Q75313281-67803DD9-5E82-4BF6-9D0B-613F541BD9D4Q77146060-17C46840-A5B0-4C54-B288-CE9FF1478BD4Q79299343-2110CE8E-5D76-4123-93CB-13B0118BDB41Q79346158-1DF66938-F0CA-458C-83E0-43DF0ACCAE30Q79433007-16D3C841-1521-48EA-9D60-ABD6E018C8F8Q80605145-CFEBC408-A584-466D-869F-70FD4879F8E5Q81321762-0ED8EABB-00AC-4619-93DB-8C912DBAF015Q81420803-0DA3160D-118C-4D92-8906-748B3BAA684E
P50
description
Russisch biochemicus
@nl
hulumtues
@sq
researcher
@en
հետազոտող
@hy
name
Viktor V. Zhdankin
@ast
Viktor V. Zhdankin
@en
Viktor V. Zhdankin
@es
Viktor V. Zhdankin
@nl
Viktor V. Zhdankin
@sl
Виктор В. Жданкин
@ru
type
label
Viktor V. Zhdankin
@ast
Viktor V. Zhdankin
@en
Viktor V. Zhdankin
@es
Viktor V. Zhdankin
@nl
Viktor V. Zhdankin
@sl
Виктор В. Жданкин
@ru
altLabel
Виктор Жданкин
@ru
Жданкин, Виктор В.
@ru
prefLabel
Viktor V. Zhdankin
@ast
Viktor V. Zhdankin
@en
Viktor V. Zhdankin
@es
Viktor V. Zhdankin
@nl
Viktor V. Zhdankin
@sl
Виктор В. Жданкин
@ru
P1053
B-6987-2008
P106
P1153
7003901979
P21
P27
P31
P3829
P496
0000-0002-0315-8861