Journal
CHEMICAL COMMUNICATIONS
Volume 54, Issue 96, Pages 13603-13606Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cc08193j
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By changing the charge distribution of boron vertices via introducing an amide on cage B(9), the selective B(4) arylation of o-carboranes via Suzuki-Miyaura coupling has been developed. A series of o-carborane derivatives decorated with diverse active groups have been synthesized with moderate to good yields, which have been proved to be further transformed to a novel kind of tri-substituted nido-carborane fused oxazole with potential application in boron neutron capture therapy, organometallic as well as coordination chemistry.
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