Intramolecular Cycloaddition of Imines of Cysteine Derivatives

Intramolecular Cycloaddition of Imines of Cysteine Derivatives

Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield.

Detaylı Bibliyografya
Asıl Yazarlar: Teresa M. V. D. Pinho e Melo, António M. d'A Rocha Gonsalves, Ana M. T. D. P. V. Cabral
Materyal Türü: Makale
Dil:English
Baskı/Yayın Bilgisi: MDPI AG 1998-02-01
Seri Bilgileri:Molecules
Konular:
Thieno[3
4-b]pyrrole derivatives
synthesis
Online Erişim:http://www.mdpi.com/1420-3049/3/3/60/

Internet

http://www.mdpi.com/1420-3049/3/3/60/

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