Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784710294363176960 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9117260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT guojunkai sulfoxfluorenableddeoxyazidationofalcoholswithnan3 AT wangxiu sulfoxfluorenableddeoxyazidationofalcoholswithnan3 AT nichuanfa sulfoxfluorenableddeoxyazidationofalcoholswithnan3 AT wanxiaolong sulfoxfluorenableddeoxyazidationofalcoholswithnan3 AT hujinbo sulfoxfluorenableddeoxyazidationofalcoholswithnan3 |