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Novel biphenol phosphoramidite ligands for the enantioselective copper-catalyzed conjugate addition of dialkyl zincs |
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Published in | Synlett. 2001, no. 9, p. 1375-1378 | |
Abstract | Phosphoramidite ligands, based on a chiral amine and atropoisomerically flexible biphenols, induce high enantioselectivities (ee's up to 98%) in the copper-catalyzed conjugate addition of dialkyl zinc reagents to a variety of Michael acceptors. | |
Keywords | 161 Biphenols Synlett 01.pdf — Asymmetric catalysis — Copper — Zinc — Michael additions — Phosphorus — Atropoisomerism | |
Identifiers | DOI: 10.1055/s-2001-16791 | |
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Citation (ISO format) | ALEXAKIS, Alexandre et al. Novel biphenol phosphoramidite ligands for the enantioselective copper-catalyzed conjugate addition of dialkyl zincs. In: Synlett, 2001, n° 9, p. 1375-1378. doi: 10.1055/s-2001-16791 https://archive-ouverte.unige.ch/unige:6318 |