
TY  - JOUR
A1  - Galteri, M 
A1  - Lewis, PH 
A1  - Middleton, S 
A1  - Stock, LE 
T1  - Stereochemical studies. VI. Stereoselective synthesis of <I>trans</I>-fused octahydroindene-1-carboxylic acids
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1980
VL  - 33
IS  - 1
SP  - 101
EP  - 111
KW  - 
UR  - https://doi.org/10.1071/CH9800101 
N2  - 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. 
ER  -

