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      Organocatalytic enantioselective formal synthesis of bromopyrrole alkaloids via aza-Michael addition

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      Organic & Biomolecular Chemistry
      Royal Society of Chemistry (RSC)

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          Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine

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            Organocatalytic asymmetric aza-Michael additions.

            The catalytic aza-Michael addition is an important reaction within synthetic organic chemistry, given the significance of the biologically and synthetically interesting products, such as beta-amino acids and beta-lactams. In the last decade organocatalysis emerged as a powerful tool in asymmetric synthesis and had a large impact on the development of asymmetric and catalytic conjugate additions of nitrogen nucleophiles to Michael acceptors. In this review a first summary of the recent rapid progress of asymmetric organocatalyzed aza-Michael reactions is presented.
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              Sixty years of staudinger reaction

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                Author and article information

                Journal
                OBCRAK
                Organic & Biomolecular Chemistry
                Org. Biomol. Chem.
                Royal Society of Chemistry (RSC)
                1477-0520
                1477-0539
                2011
                2011
                : 9
                : 22
                : 7734
                Article
                10.1039/c1ob06078c
                5a4135a7-bd02-4ce3-be82-65d91283fc50
                © 2011
                History

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