Preparation of axially chiral biphenyl diphosphine ligands and their application in asymmetric hydrogenation

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Abstract

Axially chiral biphenyldiphosphine ligands bearing diphenylphosphino group(s) and/or dicyclohexylphosphino group(s) were prepared in enantiomerically pure form starting from 2,6-dimethylnitrobenzene via 8 steps: iodination, reduction, methoxylation through diazotization, Ullmann coupling, bromination, phosphorylation, optical resolution, and silane reduction, and the obtained ligands were used in rhodium-catalyzed asymmetric hydrogenation. © 2004 Pharmaceutical Society of Japan.

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Morimoto, T., Yoshikawa, K., Murata, M., Yamamoto, N., & Achiwa, K. (2004). Preparation of axially chiral biphenyl diphosphine ligands and their application in asymmetric hydrogenation. Chemical and Pharmaceutical Bulletin, 52(12), 1445–1450. https://doi.org/10.1248/cpb.52.1445

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