Exploiting C3-symmetry in the dynamic coordination of a chiral trisoxazoline to copper(ii): improved enantioselectivity, and catalyst stability in asymmetric lewis acid catalysis

Literature Information

Publication Date 2005-09-16
DOI 10.1039/B509571A
Impact Factor 6.222
Authors

Guido Marconi, Stéphane Bellemin-Laponnaz, Hubert Wadepohl


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Abstract

Chiral C3-symmetric trisoxazolines are highly efficient stereodirecting ligands in enantioselective CuII Lewis acid catalysis which is based on the concept of a stereoelectronic hemilability of the divalent copper; in direct comparison with the analogous bisoxazoline systems they are more efficient in the enantioselective α-amination as well as the enantioselective Mannich reaction of prochiral β-ketoesters.

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Chemical Communications

Chemical Communications
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