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

YAVUZ S., ÖZKAN H., Tok G., DİŞLİ A.

JOURNAL OF HETEROCYCLIC CHEMISTRY, cilt.50, sa.6, ss.1437-1440, 2013 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 50 Sayı: 6
Basım Tarihi: 2013
Doi Numarası: 10.1002/jhet.1540
Dergi Adı: JOURNAL OF HETEROCYCLIC CHEMISTRY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.1437-1440
Gazi Üniversitesi Adresli: Evet

Özet

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.