Enantiomeric products formed via different mechanisms: asymmetric hydrogenation of an α,β-unsaturated carboxylic acid involving a Ru(CH3COO)2[(R)-binap] catalyst-Reference-Cited by-同舟云学术

Enantiomeric products formed via different mechanisms: asymmetric hydrogenation of an α,β-unsaturated carboxylic acid involving a Ru(CH3COO)2[(R)-binap] catalyst

Published:2007-11 Issue:46 Volume:63 Page:11399-11409
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Yoshimura Masahiro,Ishibashi Yoshitaka,Miyata Kengo,Bessho Yuhki,Tsukamoto Masaki,Kitamura Masato

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. Über die Reaktionsgeschwindigkeit bei der Inversion von Rohrzucker durch Säuren

2. Mechanism of Asymmetric Hydrogenation of α-(Acylamino)acrylic Esters Catalyzed by BINAP−Ruthenium(II) Diacetate

3. Observation of a [RuCl2((S)-(-)-tol-binap)]2.cntdot.N(C2H5)3-Catalyzed Isomerization-Hydrogenation Network

4. Kinetic influences on enantioselectivity in asymmetric catalytic hydrogenation

5. Enantioselective Hydrogenations of Arylalkenes Mediated by [Ir(cod)(JM-Phos)]+ Complexes

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