Issue 12, 2012

An efficient pyrroline annulation of glycine imine with enones

Abstract

We describe here a single-step synthesis of substituted 1-pyrrolines from N-(4-chlorobenzylidene)-glycine methyl ester and enones which combines conversion of the Michael adducts to 1-pyrrolines with separation between the products on silica gel column chromatography.

Graphical abstract: An efficient pyrroline annulation of glycine imine with enones

Supplementary files

Article information

Article type
Communication
Submitted
18 Apr 2012
Accepted
19 Apr 2012
First published
17 May 2012

RSC Adv., 2012,2, 5138-5140

An efficient pyrroline annulation of glycine imine with enones

Y. Zhang, L. Pan, X. Xu and Q. Liu, RSC Adv., 2012, 2, 5138 DOI: 10.1039/C2RA20697H

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements