Regioselectivity of (3+2) cycloaddition of azomethine ylides to activated olefins in the synthesis of spiro[oxindole-3,2′-pyrrolidine] derivatives

Regioselectivity of (3+2) cycloaddition of azomethine ylides to activated olefins in the synthesis of spiro[oxindole-3,2′-pyrrolidine] derivatives Review

Journal

Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122

Output data

Year: 2020, Volume: 56, Number: 3, Pages: 255-264 Pages count : 10 DOI: 10.1007/s10593-020-02654-z

Authors

Izmest’ev Alexei N. ¹ , Gazieva Galina А. ¹ , Kravchenko Angelina N. ^1,2

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russia;
2	Plekhanov Russian University of Economics, Moscow, Russia

The effect of the structure of the starting compounds on the regioselectivity of the (3+2) cycloaddition of azomethine ylides to olefins activated by electron-withdrawing groups in the synthesis of spiro[oxindole-3,2′-pyrrolidine] derivatives is generalized and analyzed.

Izmest’ev A.N. , Gazieva G.А. , Kravchenko A.N.
Regioselectivity of (3+2) cycloaddition of azomethine ylides to activated olefins in the synthesis of spiro[oxindole-3,2′-pyrrolidine] derivatives
Chemistry of Heterocyclic Compounds. 2020. V.56. N3. P.255-264. DOI: 10.1007/s10593-020-02654-z WOS Scopus OpenAlex

≡ Web of science:	WOS:000526185200001
≡ Scopus:	2-s2.0-85083863444
≡ OpenAlex:	W3016589046