Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 4, Issue 8, Pages 1636-1639Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7qo00238f
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Funding
- NSFC [21472072, 21302077, 21290183]
- Program for Changjiang Scholars and Innovative Research Team in University [PCSIRT: IRT_15R28]
- FRFCU [lzujbky-2016-ct02, lzujbky-2014-188]
- 111 Program of MOE
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A new route to arylhydrazides involving the reaction of two highly active intermediates, the 1,3-zwitterion generated in situ from the Mitsunobu reagent and arynes, under mild conditions has been developed. Further transformations of the versatile arylhydrazides to diverse nitrogen-containing heterocycles in one pot are also demonstrated.
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