4.4 Article

Pd-Catalyzed Asymmetric Alkylation of Methylphenylphosphine with Alkyl Halides for the Synthesis of P-stereogenic Compounds

期刊

CHINESE JOURNAL OF ORGANIC CHEMISTRY
卷 33, 期 4, 页码 799-802

出版社

SCIENCE PRESS
DOI: 10.6023/cjoc201301050

关键词

P-stereogenic compound; Pincer-Pd catalyst; methylphenylphosphine; asymmetric alkylation

资金

  1. National Basic Research Program of China (973 Program) [2010CB833300]
  2. National Natural Science Foundation of China [20902099, 21172238]
  3. Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

向作者/读者索取更多资源

A bis(phosphine) (PCP) pincer palladium-catalyzed asymmetric alkylation of methylphenylphosphine with alkyl halides was developed for the synthesis of P-chiral phosphorus compounds in mild conditions. The corresponding products were obtained in high yields with moderate enantioselectivities. The possible catalytic cycle and stereochemical pathway have also been proposed via the Pincer-PdPMe(Ph) intermediate, which is generated from the reaction of Pd catalyst with methylphenylphosphine.

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