Journal
SCIENCE CHINA-CHEMISTRY
Volume 65, Issue 4, Pages 678-685Publisher
SCIENCE PRESS
DOI: 10.1007/s11426-021-1170-2
Keywords
amination; photoredox; light alkane; nitrobenzene
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Funding
- National Natural Science Foundation of China [21772085, 21971107, 2201101]
- China Postdoctoral Science Foundation [2021T140309, 2021M691511]
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This study presents a rapid method for constructing C-N bonds from accessible nitroarene and alkane feedstock using decatungstate catalysis. Various types of C-H precursors can be efficiently converted into the corresponding alkylamines using this protocol.
Alkylamines are important motifs in pharmaceutical and material sciences. The existing reports of C-H amination are limited to ammonia, diazo and azide nitrogen sources. This work describes a rapid construction of C-N bonds from accessible nitroarene and alkane feedstock under decatungstate catalysis. A variety of C-H precursors including gaseous, linear, cyclic and benzylic hydrocarbons could adopt this protocol to afford the corresponding alkylamines in high efficiency
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