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Chiral-at-metal organolanthanides: enantioselective aminoalkene hydroamination/cyclisation with non-cyclopentadienyls

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UNSPECIFIED. (2003) Chiral-at-metal organolanthanides: enantioselective aminoalkene hydroamination/cyclisation with non-cyclopentadienyls. CHEMICAL COMMUNICATIONS (14). pp. 1770-1771. ISSN 1359-7345

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Official URL: http://dx.doi.org/10.1039/b305105f

Abstract

Chiral non-racemic complexes [ML{N(SiMe2H)(2)}(thf)] ( M = Y, La, H2L = salicylaldimine ligands derived from 2,2'-diamino-6,6- dimethylbiphenyl) are found not to be effective catalysts for the intramolecular hydroamination of aminoalkenes, but new amino/phenoxide ligand designs without reducible functional groups led to long-lived and enantioselective catalysts.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: CHEMICAL COMMUNICATIONS
Publisher: ROYAL SOC CHEMISTRY
ISSN: 1359-7345
Date: 2003
Number: 14
Number of Pages: 2
Page Range: pp. 1770-1771
Identification Number: 10.1039/b305105f
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/9587

Data sourced from Thomson Reuters' Web of Knowledge

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