Chelucci, Giorgio and Gladiali, Serafino and Sanna, Maria G. and Brunner, Henri (2000) Chiral ligands with pyridine donors in transition metal catalyzed enantioselective cyclopropanation and hydrosilylation reactions. TETRAHEDRON-ASYMMETRY, 11 (16). pp. 3419-3426. ISSN 0957-4166
Full text not available from this repository.Abstract
Copper(I) and rhodium(I) complexes prepared in situ from [Cu(OTf)(C6H6)(0.5)] and [Rh(cod)Cl](2) with a range of chiral 2,2'-bipyridines, 5,6-dihydro-1,10-phenanthrolines, 1,10-phenanthrolines and 2,2':6',2 "-terpyridines were assessed as chiral catalysts for the enantioselective cyclopropanation of styrene with diazoacetates and for the hydrosilylation of acetophenone with diphenylsilane. Enantioselectivities up to 68% in the cyclopropanation and up to 32% in the hydrosilylation were obtained. (C) 2000 Published by Elsevier Science Ltd.
Item Type: | Article |
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Uncontrolled Keywords: | ACTIVE NITROGEN LIGANDS; ASYMMETRIC CATALYSIS; ALLYLIC SUBSTITUTION; 2,2'-BIPYRIDINE; KETONES; OLEFINS; |
Subjects: | 500 Science > 540 Chemistry & allied sciences |
Divisions: | Chemistry and Pharmacy > Institut für Anorganische Chemie > Alumni or Retired Professors > Prof. Dr. Henri Brunner |
Depositing User: | Dr. Gernot Deinzer |
Date Deposited: | 29 Mar 2022 05:18 |
Last Modified: | 29 Mar 2022 05:18 |
URI: | https://pred.uni-regensburg.de/id/eprint/42265 |
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