Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
An Efficient Method for Selective Acetylation of Alcoholic Hydroxyl Groups
YOSHIMITSU NAGAOEIICHI FUJITATATSUHIKO KOHNOMASAHIRO YAGI
Author information
Keywords: diterpene
JOURNAL FREE ACCESS

1981 Volume 29 Issue 11 Pages 3202-3207

Details
Abstract
Acetylation of the C-6 hydroxyl group in oridonin (1), which is difficult by the use of acetic anhydride in pyridine, was investigated using acetic anhydride in the presence of some Lewis acids. A reagent system of acetic anhydride in the presence of a catalytic amount of boron trifluoride etherate was shown to be effective for this purpose. This reagent system was shown to be useful for selective acetylation of the alcoholic group (s) in compounds which have both alcoholic and phenolic hydroxyl groups.
Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top