4.8 Article

Catalytic Enantioselective Methylene C(sp3)-H Amidation of 8-Alkylquinolines Using a Cp*RhIII/Chiral Carboxylic Acid System

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 50, 页码 18154-18158

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201911268

关键词

asymmetric catalysis; C-H activation; chiral carboxylic acid; quinoline; rhodium

资金

  1. JSPS KAKENHI [JP15H05802, JP18H04637, JP17H03049, JP19K16306]

向作者/读者索取更多资源

Catalytic enantioselective directed methylene C(sp(3))-H amidation reactions of 8-alkylquinolines using a Cp*Rh-III/chiral carboxylic acid (CCA) hybrid catalytic system are described. A binaphthyl-based chiral carboxylic acid efficiently differentiates between the enantiotopic methylene C-H bonds, which leads to the formation of C-N bonds with good enantioselectivity.

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