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Title: Highly enantioselective conjugate additions to alpha,beta-unsaturated ketones catalyzed by a (salen)Al complex. Author: Taylor MS, Zalatan DN, Lerchner AM, Jacobsen EN. Journal: J Am Chem Soc; 2005 Feb 02; 127(4):1313-7. PubMed ID: 15669872. Abstract: Chiral (salen)Al complex 1a catalyzes the highly enantioselective conjugate addition of carbon- and nitrogen-based nucleophiles to acyclic alpha,beta-unsaturated ketones. This methodology is tolerant of substantial variation of the ketone structure, providing access to a wide range of useful chiral building blocks in high yield and enantiomeric excess. Synthetic manipulations of the conjugate addition products are demonstrated, including the straightforward preparation of beta-amino ketones and highly enantioenriched carbo- and heterocyclic compounds.[Abstract] [Full Text] [Related] [New Search]