
TY  - JOUR
A1  - Cambie, RC 
A1  - Coddington, JM 
A1  - Rutledge, PS 
A1  - Taylor, CM 
A1  - Woodgate, PD 
T1  - Chemistry of the Podocarpaceae. LXXV. The Conversion of 2-Oxomanoyl Oxide Into 2-oxo-&#947;-bicyclohomofarnesal
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1989
VL  - 42
IS  - 7
SP  - 1115
EP  - 1124
KW  - 
UR  - https://doi.org/10.1071/CH9891115 
N2  - 2-Oxomanoyl oxide (6) has been converted into 2-oxo-13,14,15,16-tetranorlabd-8(17)-en-12-al (2), an oxygenated analogue of the ambergris odorant, &#947;-bicyclohomofarnesal (1). The acetoxy acid (10), a key intermediate in the sequence, has been synthesized by an improved route in 75% overall yield from (6). 
ER  -

