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SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)

Direct deoxyazidation of alcohols with NaN(3) is a straightforward method for the synthesis of widely used alkyl azides in organic chemistry. However, known methods have some limitations such as high reaction temperatures and narrow substrate scope. Herein, a general and practical method for the pre...

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Detalles Bibliográficos
Autores principales: Guo, Junkai, Wang, Xiu, Ni, Chuanfa, Wan, Xiaolong, Hu, Jinbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117260/
https://www.ncbi.nlm.nih.gov/pubmed/35585073
http://dx.doi.org/10.1038/s41467-022-30132-x
Descripción
Sumario:Direct deoxyazidation of alcohols with NaN(3) is a straightforward method for the synthesis of widely used alkyl azides in organic chemistry. However, known methods have some limitations such as high reaction temperatures and narrow substrate scope. Herein, a general and practical method for the preparation of alkyl azides from alcohols using NaN(3) has been developed. N-tosyl-4-chlorobenzenesulfonimidoyl fluoride (SulfoxFluor) plays an important role in this deoxyazidation process, which converts a broad range of alcohols into alkyl azides at room temperature. The power of this deoxyazidation protocol has been demonstrated by successful late-stage deoxyazidation of natural products and pharmaceutically relevant molecules.