15973-48-5Relevant academic research and scientific papers
Borinic Acid Catalyzed, Regioselective Chloroacylations and Chlorosulfonylations of 2,3-Epoxy Alcohols
Tanveer, Kashif,Jarrah, Kareem,Taylor, Mark S.
, p. 3482 - 3485 (2015/07/28)
In the presence of a borinic acid derived catalyst, 2,3-epoxy alcohols undergo couplings with acyl and sulfonyl chlorides. This transformation directly generates O-acylated or O-sulfonylated chlorohydrin diols, with significant levels of regioselectivity for both the ring-opening and O-functionalization steps.
