Journal
RSC ADVANCES
Volume 6, Issue 16, Pages 13010-13013Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra26588f
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Funding
- National Natural Science Foundation of China [21172185, 21372187, 21572194]
- Hunan Provincial Innovative Foundation for Postgraduate [CX2014B258]
- Research Fund for the Doctoral Program of Higher Education of China, Ministry of Education of China [20124301110005]
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A palladium-catalyzed construction for N-arylsulfonamide from nitroarenes and arylsulfonyl hydrazides is developed. In this protocol, abundant and stable nitroarenes serve as the nitrogen sources by in situ reduction reaction of hydrogen released from arylsulfonyl hydrazides. No external oxidants or reductants are needed for this kind of transformation.
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