
TY  - JOUR
A1  - Bendall, JG 
A1  - Cambie, RC 
A1  - Rutledge, PS 
A1  - Woodgate, PD 
T1  - Synthesis of a Nagilactone Analog From Totarol
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1992
VL  - 45
IS  - 6
SP  - 1005
EP  - 1019
KW  - 
UR  - https://doi.org/10.1071/CH9921005 
N2  - Totarol(1) has been converted into the nagilactone-A analogue (25) by oxidative decarboxylation of the acid (18). Acid (18) was formed from the benzyl ester (20) after removal of the protecting group by hydrogenolysis, thereby circumventing a difficult hydrolysis step encountered in a previous conversion of the methyl ester (19) into (25). 
ER  -

