期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 134, 期 22, 页码 9110-9113出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja303527m
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We report the direct amidation of arene C-H bonds using sulfonyl azides as the amino source to release N-2 as the single byproduct. The reaction is catalyzed by a cationic rhodium complex under external oxidant-free conditions in the atmospheric environment. A broad range of chelate group-containing arenes are selectively amidated with excellent functional group tolerance, thus opening a new avenue to practical intermolecular C-N bond formation.
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