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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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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
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author Guo, Junkai
Wang, Xiu
Ni, Chuanfa
Wan, Xiaolong
Hu, Jinbo
author_facet Guo, Junkai
Wang, Xiu
Ni, Chuanfa
Wan, Xiaolong
Hu, Jinbo
author_sort Guo, Junkai
collection PubMed
description 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.
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spelling pubmed-91172602022-05-20 SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3) Guo, Junkai Wang, Xiu Ni, Chuanfa Wan, Xiaolong Hu, Jinbo Nat Commun Article 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. Nature Publishing Group UK 2022-05-18 /pmc/articles/PMC9117260/ /pubmed/35585073 http://dx.doi.org/10.1038/s41467-022-30132-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Guo, Junkai
Wang, Xiu
Ni, Chuanfa
Wan, Xiaolong
Hu, Jinbo
SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)
title SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)
title_full SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)
title_fullStr SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)
title_full_unstemmed SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)
title_short SulfoxFluor-enabled deoxyazidation of alcohols with NaN(3)
title_sort sulfoxfluor-enabled deoxyazidation of alcohols with nan(3)
topic Article
url 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
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