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An enantioselective strategy to macrocyclic bisindolylmaleimides. An efficient formal synthesis of LY 333531
Authors:Trost B M  Tang W
Institution:Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. bmtrost@leland.stanford.edu
Abstract:reaction: see text]. The ability to employ a bromo alcohol as a nucleophile in a palladium-catalyzed dynamic kinetic asymmetric transformation leads to an efficient synthesis of a selective PKC inhibitor under clinical development.
Keywords:
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