C2-BIPNOR: An Easily Accessible Homologue of BIPNOR for Asymmetric Catalysis-Reference-Cited by-同舟云学术

C2-BIPNOR: An Easily Accessible Homologue of BIPNOR for Asymmetric Catalysis

Published:2006-04-11 Issue:10 Volume:25 Page:2585-2589
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Siutkowski Magali¹,Mercier François¹,Ricard Louis¹,Mathey François¹

Affiliation:

1. Laboratoire “Hétéroéléments et Coordination” UMR CNRS 7653, DCPH, Ecole Polytechnique, 91128 Palaiseau Cedex, France, and UCR-CNRS Joint Research Chemistry Laboratory, Department of Chemistry, University of California Riverside, California 92521-0403

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om060118%2B

Reference10 articles.

1. Preparation and use of C2-symmetric bis(phospholanes): production of .alpha.-amino acid derivatives via highly enantioselective hydrogenation reactions

2. Synthesis of 1,1′-Bis(phosphetano)ferrocenes, a New Class of Chiral Ligands for Asymmetric Catalysis

3. Chiral 1,1′-Diphosphetanylferrocenes: New Ligands for Asymmetric Catalytic Hydrogenation of Itaconate Derivatives

4. Highly Enantioselective Hydrogenation of Simple Ketones Catalyzed by a Rh-PennPhos Complex

5. BIPNOR: A New, Efficient Bisphosphine Having Two Chiral, Nonracemizable, Bridgehead Phosphorus Centers for Use in Asymmetric Catalysis

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