Issue 19, 1985

Application of the Pictet–Spengler condensation in enantioselective synthesis of isoquinoline alkyloids

Abstract

The reaction of dopamine hydrochloride and (R)-(+)-glyceraldehyde afforts a condensation product which is a useful intermediate in the enantioselective synthesis of isoquinoline alkaloids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1318-1319

Application of the Pictet–Spengler condensation in enantioselective synthesis of isoquinoline alkyloids

Z. Czarnocki, D. B. MacLean and W. A. Szarek, J. Chem. Soc., Chem. Commun., 1985, 1318 DOI: 10.1039/C39850001318

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