Issue 9, 1986

The first natural 2,3-cis-dihydroflavonol and rationalisation of the biogenesis of 2,3-cis-proanthocyanidins

Abstract

(-)-2,3-cis-3,3′,4′,7,8-Pentahydroxyflavanone isolated from Acacia melanoxylon represents the first example of a natural dihydroflavonol with the 2,3-cis-configuration and its identification enables a more satisfactory rationalisation to be made of the biogenesis of proanthocyanidins with the 2,3-cis-monomeric units.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 675-677

The first natural 2,3-cis-dihydroflavonol and rationalisation of the biogenesis of 2,3-cis-proanthocyanidins

L. Y. Foo, J. Chem. Soc., Chem. Commun., 1986, 675 DOI: 10.1039/C39860000675

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