Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 4, Pages 1222-1225Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja411379e
Keywords
-
Categories
Funding
- National Institutes of Health (NIH) [2R01GM068433]
- Alexander von Humboldt Foundation
- Grants-in-Aid for Scientific Research [23225002] Funding Source: KAKEN
Ask authors/readers for more resources
A simple, efficient, and environmentally friendly asymmetric epoxidation of primary, secondary, tertiary allylic, and homoallylic alcohols has been accomplished. This process was promoted by a tungsten-bishydroxamic acid complex at room temperature with the use of aqueous 30% H2O2 as oxidant, yielding the products in 84-98% ee.
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
Share Paper
