Journal
ORGANIC LETTERS
Volume 12, Issue 20, Pages 4678-4681Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol102010h
Keywords
-
Categories
Funding
- The University of Notugham [NRF5012]
- The Royal Society [RG090319]
- EPRSC [EP/11018034/1]
- EPSRC [EP/H018034/1] Funding Source: UKRI
Ask authors/readers for more resources
A stereospecific triphenylphosphine oxide-catalyzed 1,2-dichlorination reaction of epoxides has been developed. The reaction is effective for a range of terminal and internal epoxides In contrast to the classical Appel-type dichlorination of epoxides, oxalyl chloride is used as a stoichrometric reagent to generate the chlorophosphonium salt responsible for dichlorination from catalytic triphenylphosphine oxide.
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