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Iron-catalyzed carboazidation of alkenes and alkynes

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...

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Detalles Bibliográficos
Autores principales: Xiong, Haigen, Ramkumar, Nagarajan, Chiou, Mong-Feng, Jian, Wujun, Li, Yajun, Su, Ji-Hu, Zhang, Xinhao, Bao, Hongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328574/
https://www.ncbi.nlm.nih.gov/pubmed/30631054
http://dx.doi.org/10.1038/s41467-018-07985-2
Descripción
Sumario: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.