期刊
ORGANIC LETTERS
卷 22, 期 7, 页码 2816-2821出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c00809
关键词
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资金
- National Natural Science Foundation of China [21801029, 81760624, 21702241]
- Graduate Scientific Research and Innovation Foundation of Chongqing [CYS18046]
- 100 Talent Plan from Chongqing University [0247001104405]
- Natural Science Foundation of Chongqing [cstc2019jcyjmsxmX0048]
- Sichuan Key Laboratory of Medical Imaging (North Sichuan Medical College) [SKLMI201901]
- Programs of Guizhou Province [2017-1225, 2018-1427]
To date, the iron-catalyzed construction of C-heteroatom bonds has been less developed due to the difficulty of transmetalation with heteroatom anions and the sluggish reductive elimination. Herein we report an iron-catalyzed method for the silylation of (hetero)aromatic chlorides. It features high efficiency, a broad substrate scope, and excellent functional group compatibility. Moreover, this protocol enables the late-stage silylation of some pharmaceuticals, thus providing an excellent method to access valuable intermediates in medicinal chemistry.
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