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Rhodium and copper-catalyzed asymmetric conjugate addition of alkenyl nucleophiles

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Published in Chemical Communications. 2012, vol. 48, no. 99, p. 12037-12049
Abstract Since the initial reports in the mid-90s, metal catalyzed asymmetric conjugate addition (ACA) reactions evolved as an important tool for the synthetic chemist. Most of the research efforts have been done in the field of rhodium and copper catalyzed ACA reactions employing aryl and alkyl nucleophiles. Despite the great synthetic value of the double bond, the addition of alkenyl nucleophiles remains insufficiently explored. In this account, an overview of the developments in the field of rhodium and copper catalyzed ACA reactions with organometallic alkenyl reagents (B, Mg, Al, Si, Zr, Sn) will be provided. The account is intended to give a comprehensive overview of all the existing methods. However, in many cases only selected examples are displayed in order to facilitate comparison of different ligands and methodologies.
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Other version: http://xlink.rsc.org/?DOI=c2cc34607a
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MUELLER, Daniel, ALEXAKIS, Alexandre. Rhodium and copper-catalyzed asymmetric conjugate addition of alkenyl nucleophiles. In: Chemical Communications, 2012, vol. 48, n° 99, p. 12037-12049. https://archive-ouverte.unige.ch/unige:24330

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Deposited on : 2012-12-05

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