4.6 Article

Ferrocene-based bifunctional organocatalyst for highly enantioselective intramolecular Rauhut-Currier reaction

期刊

CATALYSIS COMMUNICATIONS
卷 121, 期 -, 页码 78-83

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.catcom.2018.12.016

关键词

Ferrocene-based organocatalyst; Rauhut-Currier reaction; Bifunctional chiral phosphine; Enantioselective

资金

  1. National Natural Science Foundation of China [21272271, 21472240]

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Three series of novel ferrocene-based bifunctional chiral phosphines have been designed and synthesized. Thethiourea-phosphine A7 showed good performance in enantioselective intramolecular Rauhut Currier reaction of bis(enones), giving the corresponding products in good yield with up to 98% ee. Moreover, with amino acid derived amide-phosphine B3, optically active a-methylene-8-valerolactone was obtained in 88% yield and > 99.9% ee utilizing the enantioselective intramolecular Rauhut-Currier reaction of chalcone derivative.

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