Issue 14, 1989

A common synthetic route to the pericarbonyl and perimethylene lignan lactones dimethyl conidendrin and dimethyl retrodendrin

Abstract

An all trans 1-aryl-2-methoxycarbonyl tetralin-3-carboxylic acid synthesised in 32% overall yield can be converted, at will, to either dimethyl conidendrin or dimethyl retrodendrin in one step.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 959-960

A common synthetic route to the pericarbonyl and perimethylene lignan lactones dimethyl conidendrin and dimethyl retrodendrin

A. Gupta and R. Rodrigo, J. Chem. Soc., Chem. Commun., 1989, 959 DOI: 10.1039/C39890000959

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