Issue 9, 1990

The stereochemistry of the chemical ring-contraction of kaurenolides to gibberellins

Abstract

The reductive ring-contraction of the sulphonate ester of 7α,18-dihydroxykaurenolide with lithium aluminium hydride is shown to afford the 6-epi-7,19-dihydroxygibberell-16-ene.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2577-2579

The stereochemistry of the chemical ring-contraction of kaurenolides to gibberellins

M. Alam and J. R. Hanson, J. Chem. Soc., Perkin Trans. 1, 1990, 2577 DOI: 10.1039/P19900002577

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