Issue 17, 2000
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

C-18 Hydroxylation of gibberellins

Lewis N. Mander*a  and  Regan J. Thomsona  

* Corresponding authors

a Research School of Chemistry, Institute of Advanced Studies, The Australian National University, Canberra, Australia
E-mail: mander@rsc.anu.edu.au
Fax: +61-2-62798114

Abstract

A protocol for the hydroxylation of the 18-methyl group in gibberellins has been developed, as demonstrated by the successful synthesis of 18-hydroxy GA4 methyl ester by means of a tandem process involving the conjugate addition of alkoxide to the α-methylene lactone moiety of a ring A-seco-gibberellin followed by an intramolecular aldol reaction.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/B006044P
Article type
Communication
Submitted
26 Jul 2000
Accepted
02 Aug 2000
First published
14 Aug 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 2893-2894

Permissions

Request permissions

C-18 Hydroxylation of gibberellins

L. N. Mander and R. J. Thomson, J. Chem. Soc., Perkin Trans. 1, 2000, 2893 DOI: 10.1039/B006044P

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