Paper

A highly regio- and chemoselective synthesis of vicinal bromohydrins by ring opening of terminal epoxides with dibromoborane–dimethyl sulfide

Published Mar 1, 2007 · C. Roy, H. Brown

Journal of Organometallic Chemistry

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Abstract

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Study Snapshot

Dibromoborane-dimethyl sulfide effectively synthesizes vicinal bromohydrins with high chemo- and regioselectivity, accommodating various reducible functional groups during epoxide opening.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

A highly regio- and chemoselective synthesis of vicinal bromohydrins by ring opening of terminal epoxides with dibromoborane–dimethyl sulfide

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