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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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