Issue 4, 1991

Synthetic approaches to the naphthyl-isoquinoline alkaloids. Part 1. Dehydroancistrocladisine

Abstract

A synthesis of (±)-7-(4,5-dimethoxy-2-methyl-1-naphthyl)-6,8-dimethoxy-1,3-dimethylisoquinoline (dehydroancistrocladisine)19, the racemic form of a degradation product of the unusual naphthylisoquinoline alkaloid ancistrocladisine 3, is recorded. The key step relied on oxazoline chemistry for the construction of the biaryl linkage.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 841-844

Synthetic approaches to the naphthyl-isoquinoline alkaloids. Part 1. Dehydroancistrocladisine

M. A. Rizzacasa and M. V. Sargent, J. Chem. Soc., Perkin Trans. 1, 1991, 841 DOI: 10.1039/P19910000841

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