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

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.

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2020-03, Vol.56 (3), p.255-264
Hauptverfasser:	Izmest’ev, Alexei N., Gazieva, Galina А., Kravchenko, Angelina N.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alkaloids Alkenes Amino acids Chemistry Chemistry and Materials Science Chemistry, Organic Cycloaddition Derivatives Olefins Organic Chemistry Pharmacy Physical Sciences Regioselectivity Schiff bases Science & Technology Synthesis
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	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.
ISSN:	0009-3122 1573-8353
DOI:	10.1007/s10593-020-02654-z