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Design and synthesis of new bidentate phosphoramidite ligands for enantioselective copper-catalyzed conjugate addition of diethylzinc to enones

Journal

TETRAHEDRON-ASYMMETRY
Volume 17, Issue 19, Pages 2726-2729

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2006.10.029

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Several thioaryl- and phosphino-phosphoramidite ligands have been synthesized from commercially available beta-aminoalcohols. This new family of bidentate ligands are highly active in the enantioselective copper-catalyzed conjugate addition of diethylzinc to both cyclic and acyclic enones showing moderate to good enantiomeric excesses of up to 81%. (c) 2006 Elsevier Ltd. All rights reserved.

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