Iron-catalyzed carboazidation of alkenes and alkynes

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作者
Haigen Xiong
Nagarajan Ramkumar
Mong-Feng Chiou
Wujun Jian
Yajun Li
Ji-Hu Su
Xinhao Zhang
Hongli Bao
机构
[1] Chinese Academy of Sciences,Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, State Key Laboratory of Structural Chemistry, Center for Excellence in Molecular Synthesis, Fujian Institute of Research on the Structure of Matter
[2] University of Chinese Academy of Sciences,Hefei National Laboratory for Physical Sciences at the Microscale and Department of Modern Physics, CAS Key Laboratory of Microscale Magnetic Resonance
[3] University of Science and Technology of China,Lab of Computational Chemistry and Drug Design, Key Laboratory of Chemical Genomics
[4] Peking University Shenzhen Graduate School,undefined
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Carboazidation of alkenes and alkynes holds the promise to construct valuable molecules directly from chemical feedstock therefore is significantly important. Although a few examples have been developed, there are still some unsolved problems and lack of universal methods for carboazidation of both alkenes and alkynes. Here we describe an iron-catalyzed rapid carboazidation of alkenes and alkynes, enabled by the oxidative radical relay precursor t-butyl perbenzoate. This strategy enjoys success with a broad scope of alkenes under mild conditions, and it can also work with aryl alkynes which are challenging substrates for carboazidation. A large number of diverse structures, including many kinds of amino acid precursors, fluoroalkylated vinyl azides, other specific organoazides, and 2H-azirines can be easily produced.
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