Chiral alcoholates in asymmetric synthesis
Abstract
Enantioselective dehydrohalogenation reactions with enantiomeric excesses (e.e.) as high as 90% are promoted by chiral alcoholates as bases.
Enantioselective dehydrohalogenation reactions with enantiomeric excesses (e.e.) as high as 90% are promoted by chiral alcoholates as bases.
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J. Vadecard, J. Plaquevent, L. Duhamel and P. Duhamel, J. Chem. Soc., Chem. Commun., 1993, 116 DOI: 10.1039/C39930000116
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