Issue 22, 1985

2,5-Unsubstituted pyrrolidines from formaldehyde and amino acids through in situ azomethine-ylide 1,3-dipolar cycloaddition to alkenes

Abstract

Formaldehyde and α-amino acids such as sarcosine and glycine react with alkenes to give N-Me and N-H Pyrrolidines via in situ generated azomethine-yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1566-1567

2,5-Unsubstituted pyrrolidines from formaldehyde and amino acids through in situ azomethine-ylide 1,3-dipolar cycloaddition to alkenes

M. Joucla and J. Mortier, J. Chem. Soc., Chem. Commun., 1985, 1566 DOI: 10.1039/C39850001566

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.

Spotlight

Advertisements