Volume 29, Issue 46
Organoelement Compounds
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ChemInform Abstract: Catalytic and Structural Features of Hydroxy and Methoxy Groups as Hemilabile Coordinating Ligands in Chiral (Diphosphane)rhodium(I) Hydrogenation Catalysts.

S. BORNS

S. BORNS

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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R. KADYROV

R. KADYROV

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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D. HELLER

D. HELLER

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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W. BAUMANN

W. BAUMANN

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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A. SPANNENBERG

A. SPANNENBERG

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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R. KEMPE

R. KEMPE

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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J. HOLZ

J. HOLZ

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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A. BOERNER

A. BOERNER

Inst. Org. Katalyseforsch., Univ. Rostock, D-18055 Rostock, Germany

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First published: 18 June 2010
Citations: 1

Abstract

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ChemInform Abstract

The catalytic activity of hydroxy- and methoxy-substituted diphosphane rhodium complexes in asymmetric hydrogenation of prochiral olefins, e.g. itaconic acid, is investigated in comparison to the unsubstituted parent complex. Introduction of the methoxy substituent in (Ia) reduces seriously the reaction rate and the hydroxy substituent still enhances the loss of reactivity but leads to significantly higher enantioselectivities (by ca. 35% e.e.) than the methoxy substituent.

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