Issue 0, 1967

Phytochemical studies. Part V. The synthesis of Taiwanin A

Abstract

Conversion of dipiperonylidenesuccinic anhydride into the ethyl hydrogen ester, followed by reduction with lithium borohydride, gave a hydroxy-acid, which on treatment with toluene-p-sulphonic acid, produced taiwanin A.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 161-162

Phytochemical studies. Part V. The synthesis of Taiwanin A

G. A. Swoboda, K. Wang and B. Weinstein, J. Chem. Soc. C, 1967, 161 DOI: 10.1039/J39670000161

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