Issue 7, 1971

The synthesis of a proerythrinadienone system by phenol oxidation

Abstract

Phenol oxidation of 2-ethoxycarbonylnorprotosinomenine (II) afforded the proerythrinadienone (IV), which had a basic skeleton of the key intermediate in the biogenesis of Erythrina alkaloids.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 289-289

The synthesis of a proerythrinadienone system by phenol oxidation

T. Kametani, R. Charubala, M. Ihara, M. Koizumi and K. Fukumoto, J. Chem. Soc. D, 1971, 289 DOI: 10.1039/C29710000289

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