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Catalyst structure and the enantioselective cyclopropanation of alkenes by copper complexes of biaryldiimines: the importance of ligand acceleration
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UNSPECIFIED (2001) Catalyst structure and the enantioselective cyclopropanation of alkenes by copper complexes of biaryldiimines: the importance of ligand acceleration. TETRAHEDRON-ASYMMETRY, 12 (7). pp. 1055-1061. ISSN 0957-4166
Full text not available from this repository.Abstract
The use of chiral non-racemic biaryl copper(I) complexes in the enantioselective cyclopropanation of a number of olefins with either ethyl or tert-butyl diazoacetate: is described. Lack of ligand acceleration and the presence of equilibrium amounts of catalytically active uncomplexed Cu(I) ions account for lowered enantioselectivity when using certain ligands. (C) 2001 Elsevier Science Ltd. All rights reserved.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QD Chemistry |
| Journal or Publication Title: | TETRAHEDRON-ASYMMETRY |
| Publisher: | PERGAMON-ELSEVIER SCIENCE LTD |
| ISSN: | 0957-4166 |
| Date: | 8 May 2001 |
| Volume: | 12 |
| Number: | 7 |
| Number of Pages: | 7 |
| Page Range: | pp. 1055-1061 |
| Publication Status: | Published |
| URI: | http://wrap.warwick.ac.uk/id/eprint/12078 |
Data sourced from Thomson Reuters' Web of Knowledge
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