期刊
ORGANIC CHEMISTRY FRONTIERS
卷 8, 期 24, 页码 6923-6930出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1qo01344k
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资金
- Natural Science Foundation of Shandong Province [ZR2019BB011]
- Scientific Research Foundation of Qingdao University of Science Technology [010029022]
- JSPS KAKENHI [JP20H02730]
An enantioselective C-H alkylation of ferrocene carboxamides with diazomalonates using an achiral Cp*Ir(iii)/chiral carboxylic acid system is reported, providing planar chiral alkylated ferrocenes in good yields with moderate to good enantioselectivity (up to 94 : 6 er).
Enantioselective C-H alkylation of ferrocene carboxamides with diazomalonates using an achiral Cp*Ir(iii)/chiral carboxylic acid is described. The combination of an achiral Cp*Ir(iii) complex and a binaphthyl-based chiral carboxylic acid provided planar chiral alkylated ferrocenes in good yields with moderate to good enantioselectivity (up to 94 : 6 er).
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