ENANTIOSELECTIVE CATALYSIS .59. ADDITIONAL OF OPTICALLY-ACTIVE P-H COMPOUNDS TO P-SUBSTITUTED OLEFINS

BRUNNER, H and LIMMER, S (1991) ENANTIOSELECTIVE CATALYSIS .59. ADDITIONAL OF OPTICALLY-ACTIVE P-H COMPOUNDS TO P-SUBSTITUTED OLEFINS. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 413 (1-3). pp. 55-63. ISSN 0022-328X,

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Abstract

The base-catalyzed addition of the optically active P-H phospholanes tarpholane and diopholane to olefins activated by diphenylphosphino or diphenylphosphinoyl groups gives unsymmetrical chelate phosphines which are used as cocatalysts in the hydrogenation of (Z)-alpha-N-acetamidocinnamic acid, in the cross-coupling of 1-phenylethyl Grignard with vinylbromide, and in the hydrosilylation of acetophenone with diphenylsilane.

Item Type: Article
Uncontrolled Keywords: ASYMMETRIC CATALYSIS; TARTARIC ACID; RH-COMPLEXES; PHOSPHINES; LIGANDS; HYDROSILYLATION; HYDROGENATION; BONDS;
Depositing User: Dr. Gernot Deinzer
Last Modified: 19 Oct 2022 08:46
URI: https://pred.uni-regensburg.de/id/eprint/54919

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