Journal
ORGANIC LETTERS
Volume 15, Issue 10, Pages 2534-2537Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol401021x
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- NIH [NIGMS R01-GM-081376]
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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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