Next Article in Journal
An Asymmetric Synthetic Approach to the A-ring of the Taxol Family of Anti-Cancer Compounds
Previous Article in Journal
Efficient Polymer-Supported Sharpless Alkene Epoxidation Catalyst
Molecules 1998, 3(3), 60-63; doi:10.3390/30300060
Article

Intramolecular Cycloaddition of Imines of Cysteine Derivatives

,  and *
Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade de Coimbra, Portugal
* Author to whom correspondence should be addressed.
Received: 3 December 1997 / Accepted: 3 February 1998 / Published: 18 February 1998
Download PDF [22 KB, uploaded 18 June 2014]

Abstract

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.
Keywords: Thieno[3; 4-b]pyrrole derivatives; synthesis Thieno[3; 4-b]pyrrole derivatives; synthesis
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Share & Cite This Article

Export to BibTeX |
EndNote


MDPI and ACS Style

Cabral, A.M.T.D.P.V.; D'A Rocha Gonsalves, A.M.; Pinho e Melo, T.M.V.D. Intramolecular Cycloaddition of Imines of Cysteine Derivatives. Molecules 1998, 3, 60-63.

View more citation formats

Related Articles

Article Metrics

Comments

Citing Articles

[Return to top]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert