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Relationship between the structure and enantioselectivity in the asymmetric reduction of 2,6-disubstituted acetophenones with DIP-Chloride. An ab initio study
Authors:PVeeraraghavan Ramachandran  Baoqing Gong  Herbert C Brown  Joseph S Francisco
Institution:Herbert C. Brown Center for Borane Research, 560 Oval Drive, Department of Chemistry, Purdue University, West Lafayette, IN 47907-2084, USA
Abstract:Using computational and chemical studies, a relationship between the % ee achieved and the dihedral angles between the plane of the aromatic ring and the plane containing the carbonyl group has been established for asymmetric reductions with B-chlorodiisopinocampheylborane.
Keywords:Asymmetric reduction  B-Chlorodiisopinocampheylborane  Aralkyl ketones  Dihedral angles
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