
%0 Journal Article
%A Grant, PK 
%A Liau, HTL 
%T Diterpene chemistry. IX. Ozonolyses of Labda-8(17),14-dien-13-ol (manool) and its derivatives
%J Australian Journal of Chemistry
%D 1978/08/01
%V 31
%N 8
%P 1791-1797
%K 
%R https://doi.org/10.1071/CH9781791
%U https://www.publish.csiro.au/paper/CH9781791 
%X 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). 
