Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Diterpene chemistry. IX. Ozonolyses of Labda-8(17),14-dien-13-ol (manool) and its derivatives

PK Grant and HTL Liau

Australian Journal of Chemistry 31(8) 1791 - 1797
Published: 1978

Abstract

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 8β,13:8,14-diepoxy-15,17-dinorlabdan-14β-ol(7) was isolated as the major ozonolysis product and is a precursor of the lactone perfume (10).

https://doi.org/10.1071/CH9781791

© CSIRO 1978

Committee on Publication Ethics


Rent Article (via Deepdyve) Export Citation Cited By (5) Get Permission

View Dimensions