Kinetic Investigations of the Hydrogenation of Diolefin Ligands in Catalyst Precursors for the Asymmetric Reduction of Prochiral Olefins, II [1]-Reference-Cited by-同舟云学术

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Kinetic Investigations of the Hydrogenation of Diolefin Ligands in Catalyst Precursors for the Asymmetric Reduction of Prochiral Olefins, II [1]

Published:1996-01 Issue:1 Volume:129 Page:85-89
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Heller Detlef¹,Borns Susanne¹,Baumann Wolfgang²,Selke Rüdiger¹

Affiliation:

1. Max‐Planck‐Gesellschaft, Arbeitsgruppe „Asymmetrische Katalyse”︁ an der Universität Rostock^a, Buchbinderstraße 5/6, D‐18055 Rostock

2. Max‐Planck‐Gesellschaft, Arbeitsgruppe „Komplexkatalyse”︁ an der Universität Rostock^b, Buchbinderstraße 5/6, D‐18055 Rostock

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19961290117

Reference27 articles.

1. Dedicated to Prof. H.‐D. Scharf on the occasion of his 65th birthday. – Part I:D.Heller K.Kortus R.Selke Liebigs Ann.1995 575–581.

2. Asymmetric hydrogenation of methyl (Z)-.alpha.-acetamidocinnamate catalyzed by [1,2-bis(phenyl-o-anisoyl)phosphino)ethane]rhodium(I): kinetics, mechanism and origin of enantioselection

3. Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine

4. [4a]R.Selke G.Pracejus H.Pracejus Symp. Rhodium Homog. Catalysis Vesprem 1978 143–148.

5. Phosphinites of carbohydrates as chiral ligands for asymmetric synthesis catalyzed by complexes, I. Hydrogenation of aminoacid precursors by rhodium(I) chelates of methyl 4,6-O-benzylidente-2,3-bis-O-(diphenylphosphino)-α-D-glucopyranosides

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