Stereochemical studies. VI. Stereoselective synthesis of trans-fused octahydroindene-1-carboxylic acids
M Galteri, PH Lewis, S Middleton and LE Stock
Australian Journal of Chemistry
33(1) 101 - 111
Published: 1980
Abstract
The trans-fused octahydroindene-1-carboxylic acid (9) having a pseudo- axial carboxyl group is formed in good yield on oxidation of 2-acyl derivatives of trans-fused octahydronaphthalen-1(2H)-one. On epimerization it yields the pseudo-equatorial isomer (3) which is structurally related to the gibberellic acids.
https://doi.org/10.1071/CH9800101
© CSIRO 1980
