Discussion Addendum for: Resolution of 1,1′-Bi-2-Naphthol; (R)-(+)- and (S)-(−)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (BINAP)
Author:
Affiliation:
1. Department of Process Chemistry; Merck and Co., Inc.; Rahway NJ 07065
Publisher
John Wiley & Sons, Inc.
Reference43 articles.
1. 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
2. Developments in Asymmetric Hydrogenation from an Industrial Perspective
3. Practical synthesis of (R)- or (S)-2,2'-bis(diarylphosphino)-1,1'-binaphthyls (BINAPs)
4. (R)-(+)- AND (S)-(−)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL (BINAP)
5. BINOL: A Versatile Chiral Reagent
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1. Synthesis of Axially Chiral 2,2′-Bisphosphobiarenes via a Nickel-Catalyzed Asymmetric Ullmann Coupling: General Access to Privileged Chiral Ligands without Optical Resolution;Journal of the American Chemical Society;2021-01-13
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