Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 68, Issue 7, Pages 2968-2971Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo020653t
Keywords
-
Categories
Ask authors/readers for more resources
Ailanthoidol 1, which can be isolated from Chinese herbal medicine, is achieved in which the longest linear sequence is only six steps in 48% overall yield from commercially available 5-bromo-2-hydroxy-3-methoxybenzaldehyde. The key transformations in the synthesis are the Stille coupling reactions of benzofuranyl bromide with stannanyl compounds. This synthetic strategy can be modified to give access to a variety of different ailanthoidol and XH14 analogues.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available