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Cascade of Michael Addition/Retro‐Michael Reaction/Skeletal Rearrangement in the Synthesis of Arylmethylidene Derivatives of Imidazothiazolotriazines Full article

Journal ChemistrySelect
ISSN: 2365-6549
Output data Year: 2019, Volume: 4, Number: 35, Pages: 10483-10487 Pages count : 5 DOI: 10.1002/slct.201902461
Authors Izmest'ev Alexei N. 1 , Kim Nikita A. 2,1 , Karnoukhova Valentina A. 3 , Kolotyrkina Natalya G. 1 , Kravchenko Angelina N. 4,1 , Gazieva Galina A. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Prosp., 119991 Moscow, Russian Federation
2 D. Mendeleev University of Chemical Technology of Russia, 9 Miusskaya Sq., 125047 Moscow, Russian Federation
3 A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova Str., 119991 Moscow, Russian Federation
4 Academic Department of Chemistry and Phisics, Plekhanov Russian University of Economics, 36 Stremyanny lane, 117997 Moscow, Russian Federation

Abstract: Chemo-, regio- and diastereoselective approach to the synthesis of arylmethylideneimidazothiazolotriazines has been developed based on the Michael addition/retro-Michael reaction and Michael addition/retro-Michael reaction/skeletal rearrangement cascade processes in the reactions of imidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazines with arylmethylidene derivatives of malononitrile.
Cite: Izmest'ev A.N. , Kim N.A. , Karnoukhova V.A. , Kolotyrkina N.G. , Kravchenko A.N. , Gazieva G.A.
Cascade of Michael Addition/Retro‐Michael Reaction/Skeletal Rearrangement in the Synthesis of Arylmethylidene Derivatives of Imidazothiazolotriazines
ChemistrySelect. 2019. V.4. N35. P.10483-10487. DOI: 10.1002/slct.201902461 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000486736500040
≡ Scopus: 2-s2.0-85073244395
≡ OpenAlex: W2974396452
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