期刊
ORGANIC LETTERS
卷 18, 期 18, 页码 4686-4689出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b02326
关键词
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资金
- National Natural Science Foundation of China [21132003, 21421062, 21372131]
- Specialized Research Fund for the Doctoral Program of Higher Education [20130031110017]
- Tianjin Natural Science Foundation [16JCZDJC32400]
A direct alpha-C-H electron-deficient arylation reaction of N-acyl protected tetrahydroisoquinolines is developed via visible light photoredox catalysis. The reaction was performed under mild conditions without any extra oxidant and could also proceed smoothly when sunlight was used as the light source. The protecting group on the tetrahydroisoquinolines could be removed easily.
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