
TY  - JOUR
A1  - Grant, PK 
A1  - Liau, HTL 
T1  - Diterpene chemistry. IX. Ozonolyses of Labda-8(17),14-dien-13-ol (manool) and its derivatives
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1978
VL  - 31
IS  - 8
SP  - 1791
EP  - 1797
KW  - 
UR  - https://doi.org/10.1071/CH9781791 
N2  - Reaction of manool and its derivatives with ozone gave stable ozonides. The structure (6) of one of the ozonides isolated is of striking similarity to the perfumery acetals (1) and (2) derived from the potassium permanganate oxidation of manool (3). Another compound 8&#946;,13:8,14-diepoxy-15,17-dinorlabdan-14&#946;-ol(7) was isolated as the major ozonolysis product and is a precursor of the lactone perfume (10). 
ER  -

