A. S. KOZ'MIN - Concepedia

Author

A. S. KOZ'MIN

Also Known As

A. S. KOZ'MIN, A. S. KOZMIN, A. S. Koz'min, A. S. Kozmin, A.S. Koz'min, A.S. Kozmin, Anatoly S. Koz'min, Anatoly S. Koz`min

154

Publications

792

Citations

H-Index

Concepts

All Affiliations

Lomonosov Moscow State University Moscow State University University of Minnesota, Duluth

About

A. S. KOZ'MIN is an author at Lomonosov Moscow State University specializing in chemistry, organic chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	13	15	538
2	Biomolecular Engineering	7	7	281
3	Biochemistry	5	5	210
4	Natural Sciences	4	4	161
5	Arts	1	1	49

A. S. KOZ'MIN

Publications

633

Citations

H-Index

Page 1

	Year	Citations
Carbon-carbon bond formation in reactions of PhIO.cntdot.HBF4-silyl enol ether adduct with alkenes or silyl enol ethers Viktor V. Zhdankin, M. Mullikin, Rik R. Tykwinski, The Journal of Organic Chemistry Inorganic ChemistryChemical EngineeringNovel OrganocatalystsEngineeringChemical Analysis	1989	67
Novel reagents containing hypervalent iodine and their use for electrophilic additions to olefins N. S. Zefirov, Viktor V. Zhdankin, YU. V. DAN'KOV, Tetrahedron Letters EngineeringAlkene MetathesisElectrophilic AdditionsHypervalent IodineOrganic Chemistry	1986	67
Iodosobenzene tetrafluoroborate, hexafluoroantimonate, and hexafluorophosphate: stable electrophilic hypervalent iodine reagents without nucleophilic ligands Viktor V. Zhdankin, Rik R. Tykwinski, Bruce Berglund, The Journal of Organic Chemistry Iodosobenzene TetrafluoroborateNucleophilic LigandsEngineeringChemical AnalysisAltmetric Attention Score	1989	67
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 N. S. Zefirov, A. S. KOZ'MIN, T. M. Kasumov, The Journal of Organic Chemistry Inorganic ChemistryChemical EngineeringEngineeringAltmetric Attention ScoreOrganic Chemistry	1992	54
Competitive binding of nucleofugal anions in carbocationic-like processes A. S. KOZ'MIN Accounts of Chemical Research AltmetricsEngineeringInformation RetrievalBiochemistryEnzyme Catalysis	1985	49
<sup>13</sup>C NMR spectra of cyclopropane derivatives. Stereoisomeric substituted 2‐phenylcyclopropanes O. A. Subbotin, A. S. KOZ'MIN, Yuri K. Grishin, Organic Magnetic Resonance Derivative (Chemistry)DerivativesBiochemistryNatural SciencesAdditive Approach	1972	43
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 Viktor V. Zhdankin, Rik R. Tykwinski, Ronald Caple, Tetrahedron Letters Chemical EngineeringNovel OrganocatalystsEngineeringHypervalent Iodine ReagentsOrganometallic Catalysis	1988	42
Oxidatively assisted nucleophilic substitution of iodine in alkyl iodides by nucleofugic anions Viktor V. Zhdankin, G. V. Makhon'kova, YU. V. DAN'KOV, The Journal of Organic Chemistry HalogenationInorganic ChemistryChemical EngineeringNucleofugic AnionsEngineering	1985	39
Iodosobenzene tetrafluoroborate: First example of a stable electrophilic hypervalent iodine reagent without nucleophilic ligands Viktor V. Zhdankin, Rik R. Tykwinski, Ronald Caple, Tetrahedron Letters Iodosobenzene TetrafluoroborateInorganic ChemistryNucleophilic LigandsEngineeringOrganic Chemistry	1988	30
Electrophilic addition of arylsulfenyl chlorides to tricyclo[4.2.2.02,5]deca-3,7-diene and -3,7,9-triene systems. Novel skeletal rearrangements and serendipitous products A. S. KOZ'MIN, V.N. Kirin, Viktor V. Zhdankin, The Journal of Organic Chemistry Electrophilic AdditionEngineeringArylsulfenyl ChloridesNovel Skeletal RearrangementsAltmetric Attention Score	1981	28

Page 1