Modified BINAP: The How and the Why-Reference-Cited by-同舟云学术

Modified BINAP: The How and the Why

Published:2005-04-16 Issue:5 Volume:105 Page:1801-1836
ISSN:0009-2665
Container-title:Chemical Reviews
language:en
Short-container-title:Chem. Rev.

Author:

Berthod Mikaël¹,Mignani Gérard¹,Woodward Gary¹,Lemaire Marc¹

Affiliation:

1. Laboratoire de Catalyse et Synthèse Organique, UCBL-CPE, 43 Boulevard du 11 Novembre 1918, 69622 Villeurbanne Cedex, France, Rhodia CR de Lyon, 85 Avenue des Frères Perret, 69192 Saint Fons Cedex, France, and Rhodia PPD, Oldbury Works, Oldbury, West Midlands B69 4LN, England

Publisher

American Chemical Society (ACS)

Subject

General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cr040652w

Reference178 articles.

1. 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

2. Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of .alpha.-(acylamino)acrylic acids

3. Research by topic on SciFinder Scholar, 2004-08-27. Keyword BINAP and then refine by document type.

4. Practical synthesis of (R)- or (S)-2,2'-bis(diarylphosphino)-1,1'-binaphthyls (BINAPs)

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