期刊
ORGANIC LETTERS
卷 15, 期 10, 页码 2534-2537出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol401021x
关键词
-
资金
- NIH [NIGMS R01-GM-081376]
Sulfamates were studied as the electrophilic partners in the palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with potassium Boc-protected primary and secondary aminomethyltrifluoroborates. A broad range of substrates was successfully coupled to provide the desired products. Complex molecules containing a new carbon-carbon bond and an aminomethyl moiety could be prepared through this developed method.
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