
%0 Journal Article
%A Galteri, M 
%A Lewis, PH 
%A Middleton, S 
%A Stock, LE 
%T Stereochemical studies. VI. Stereoselective synthesis of <I>trans</I>-fused octahydroindene-1-carboxylic acids
%J Australian Journal of Chemistry
%D 1980/01/01
%V 33
%N 1
%P 101-111
%K 
%R https://doi.org/10.1071/CH9800101
%U https://www.publish.csiro.au/paper/CH9800101 
%X 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. 
