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Synlett 1992; 1992(4): 347-348
DOI: 10.1055/s-1992-22010
DOI: 10.1055/s-1992-22010
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Cohalogenation of Alkenes by N-Bromosuccinimide in Acetic Acid Derivatives: An Efficient Method for the Synthesis of trans-ß-Bromoacetic Ester Precursors of cis-1,2-diols
Further Information
Publication History
Publication Date:
08 March 2002 (online)
Alkenes 1 are converted in two steps into the mono-(diphenylacetates) of cis-1,2-diols 4, by the chemo-, regio- and stereoselective cohalogenation of alkenes by N-bromosuccinimide in diphenylacetic acid.