Synlett 1991; 1991(4): 248-250
DOI: 10.1055/s-1991-20695
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Regio- and Chemoselective Ring Opening of Epoxides to Bromohydrins with Dilithium Tetrabromocuprate

James A. Ciaccio* , Elizabeth Heller, Adrian Talbot
  • *Department of Chemistry, Fordham University, Bronx, New York 10458, USA
Further Information

Publication History

Publication Date:
07 March 2002 (online)

Dilithium tetrabromocuprate, prepared from lithium bromide and copper(II) bromide, regioselectively converts functionalized epoxides (11 examples) to vicinal bromohydrins resulting from nucleophilic attack by bromide at the less substituted epoxide carbon.

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