Facile Method for 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides: Highly Stereoselective Synthesis of Substituted Pyrrolidine Derivatives

YAVUZ, SERKAN; ÖZKAN, HAMDİ; Tok, HAMDİ; DİŞLİ, ALİ

doi:10.1002/jhet.1540

Facile Method for 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides: Highly Stereoselective Synthesis of Substituted Pyrrolidine Derivatives

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YAVUZ S., ÖZKAN H., Tok G., DİŞLİ A.

JOURNAL OF HETEROCYCLIC CHEMISTRY, vol.50, no.6, pp.1437-1440, 2013 (SCI-Expanded)

Publication Type: Article / Article
Volume: 50 Issue: 6
Publication Date: 2013
Doi Number: 10.1002/jhet.1540
Journal Name: JOURNAL OF HETEROCYCLIC CHEMISTRY
Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Page Numbers: pp.1437-1440
Gazi University Affiliated: Yes

Abstract

The substituted pyrolidine derivatives with high stereoselectivity were obtained through cycloaddition reaction in the presence of a Lewis acid namely diethylzinc by solvent-free grinding method.