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Copper-mediated asymmetric transformations

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Published in Pure and Applied Chemistry. 2002, vol. 74, no. 1, p. 37-42
Abstract Copper-catalyzed reactions include the enantioselective conjugate addition and the SN2¢ substitution. We describe the genesis of these reactions, the choice of the primary organometallic reagent, and our studies on finding new Michael acceptors and new ligands. We also report on the use of the zinc enolate generated upon conjugate addition.
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Note 11th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS-11). - Taipei (Taiwan). - 22-26 july 2001
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ALEXAKIS, Alexandre. Copper-mediated asymmetric transformations. In: Pure and Applied Chemistry, 2002, vol. 74, n° 1, p. 37-42. https://archive-ouverte.unige.ch/unige:9591

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Deposited on : 2010-07-12

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