A. N. Vereshchagin - Concepedia

Author

A. N. Vereshchagin

N.D. Zelinsky Institute of Organic Chemistry ORCID

Also Known As

A N Vereshchagin, A. N. VERESHCHAGIN, A. N. Vereshchagin, A.N. Vereshchagin, Anatolii N Vereshchagin, Anatolii N. Vereshchagin, Anatolii Vereshchagin, Anatoly N. Vereshchagin, Anatoly N. Vereshchagin, Anatoly Nikolaevich Vereshchagin

626

Publications

3.2K

Citations

H-Index

Concepts

All Affiliations

N.D. Zelinsky Institute of Organic Chemistry A. N. Nesmeyanov Institute of Organoelement Compounds A.V. Topchiev Institute of Petrochemical Synthesis D. Mendeleyev University of Chemical Technology of Russia Russian Academy of Sciences

About

A. N. Vereshchagin is an author at N.D. Zelinsky Institute of Organic Chemistry specializing in organic chemistry, chemistry, and engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	24	37	1.1K
2	Natural Sciences	14	18	497
3	Biomolecular Engineering	14	15	453
4	Medicine	7	7	149
5	Biochemistry	6	6	148

A. N. Vereshchagin

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Organoelement chemistry: promising growth areas and challenges G.A. Abakumov, Alexandr V. Piskunov, Vladimir K. Cherkasov, Russian Chemical Reviews Fine ChemicalOrganoelement ChemistrySustainable SynthesisOrganic ChemistryChemistry	2018	174
Organoelement chemistry: promising areas of growth and challenges G.A. Abakumov, Alexandr V. Piskunov, Vladimir K. Cherkasov, Russian Chemical Reviews Organic ChemistryNovel OrganocatalystsOrganoelement ChemistryChemistry	2018	76
Pot, atom and step economic (PASE) synthesis of 5-isoxazolyl-5H-chromeno[2,3-b]pyridine scaffold A. N. Vereshchagin, Michaïl N. Elinson, Yuliya E. Anisina, Mendeleev Communications	2015	54
Chemical and electrocatalytic cascade cyclization of salicylaldehyde with three molecules of malononitrile: ‘one-pot’ simple and efficient way to the chromeno[2,3-b]pyridine scaffold Michaïl N. Elinson, Sergey V. Gorbunov, A. N. Vereshchagin, Tetrahedron Chemical EngineeringEngineeringElectrocatalytic Cascade CyclizationElectrosynthesisOrganic Chemistry	2014	53
Electrochemical synthesis of cyclopropanes Michaïl N. Elinson, Evgeniya O. Dorofeeva, A. N. Vereshchagin, Russian Chemical Reviews Chemical EngineeringNovel OrganocatalystsEngineeringHeterocyclicOrganic Electrochemistry	2014	51
Electrocatalysis in MIRC reaction strategy: facile stereoselective approach to medicinally relevant spirocyclopropylbarbiturates from barbituric acids and activated olefins Evgeniya O. Dorofeeva, Michaïl N. Elinson, A. N. Vereshchagin, RSC Advances EngineeringBarbituric AcidsOrganic ChemistryChemistryMedicinal Chemistry	2012	47
Electrocatalytic and chemical methods in MHIRC reactions: the first example of the multicomponent assembly of medicinally relevant spirocyclopropylbarbiturates from three different molecules A. N. Vereshchagin, Michaïl N. Elinson, Evgeniya O. Dorofeeva, Tetrahedron Medicinal ChemistryEngineeringNatural SciencesMhirc ReactionsChemical Methods	2012	47
Electrocatalytic stereoselective transformation of aldehydes and two molecules of pyrazolin-5-one into (R,R)-bis(spiro-2,4-dihydro-3H-pyrazol-3-one)cyclopropanes Michaïl N. Elinson, Evgeniya O. Dorofeeva, A. N. Vereshchagin, Catalysis Science & Technology Asymmetric CatalysisChemical EngineeringEngineeringHeterocyclicOrganic Chemistry	2015	45
A new strategy of the chemical route to the cyclopropane structure: direct transformation of benzylidenemalononitriles and malononitrile into 1,1,2,2-tetracyanocyclopropanes Michaïl N. Elinson, Sergey K. Feducovich, Nikita O. Stepanov, Tetrahedron EngineeringHeterocyclicCyclopropane StructureChemical RouteOrganic Chemistry	2007	42
Electrocatalytic cascade multicomponent assembling: stereoselective one-pot synthesis of the substituted 3-azabicyclo[3.1.0]hexane-1-carboxylate system from aldehyde, malononitrile, malonate and methanol A. N. Vereshchagin, Michaïl N. Elinson, Tatiana A. Zaimovskaya, Tetrahedron Chemical EngineeringStereoselective One-pot SynthesisEngineeringNatural SciencesDiversity-oriented Synthesis	2008	42

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