Chiral ligands with pyridine donors in transition metal catalyzed enantioselective cyclopropanation and hydrosilylation reactions

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

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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
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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