期刊
ORGANIC LETTERS
卷 21, 期 9, 页码 2993-2997出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b00442
关键词
-
资金
- MOST [2015CB856600]
- NSFC [21602214]
In the presence of visible-light photoredox and chiral phosphate catalysts, a novel asymmetric Friedel-Crafts reaction of indoles and readily accessible alpha-amino acid derived redox-active esters is established to afford enantioenriched-1- indolyl-1-alkylamine derivatives in moderate to high yields and with high levels of enantioselectivities. This method not only shows a mild and efficient alternative for the in situ generation of N-acyl imines but also indicates the feasibility of a multicatalyst system for asymmetric photoredox catalysis.
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