Journal
CHEMICAL COMMUNICATIONS
Volume 51, Issue 56, Pages 11202-11205Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc03497c
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Funding
- Institute for Basic Science [IBS-R010-G1]
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An efficient Rh(III)-catalyzed 7-azaindole synthesis was developed via C-H activation/annulative coupling of aminopyridines with alkynes. The reaction was highly regioselective and tolerated various functional groups, permitting the construction of various 7-azaindoles.
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