Issue 0, 1984

The conversion of gibberellic acid into steroid analogues

Abstract

The expansion of ring B of the gibberellins by formolysis of the toluene-p-sulphonate of the 7-hydroxymethyl analogue of gibberic acid affords the steroid analogue, 4-methyl-15(14→8α)-abeo-16-noroestra-1,3,5(10)-trien-17-one.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1984, 2173-2176

The conversion of gibberellic acid into steroid analogues

J. R. Hanson and L. Yang-zhi, J. Chem. Soc., Perkin Trans. 1, 1984, 2173 DOI: 10.1039/P19840002173

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