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Methods for direct C(sp(2))–H bonds azidation
Direct functionalization of C–H bonds has attracted great attention in recent years from the perspectives of atom and step economy. In this context, a variety of processes have been developed for the construction of synthetically and biologically important organic azides through the oxidative C–H bo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069887/ https://www.ncbi.nlm.nih.gov/pubmed/35528700 http://dx.doi.org/10.1039/c9ra04534a |
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author | Liu, Ying Ebadi, Abdol Ghaffar Youseftabar-Miri, Leila Hassanpour, Akbar Vessally, Esmail |
author_facet | Liu, Ying Ebadi, Abdol Ghaffar Youseftabar-Miri, Leila Hassanpour, Akbar Vessally, Esmail |
author_sort | Liu, Ying |
collection | PubMed |
description | Direct functionalization of C–H bonds has attracted great attention in recent years from the perspectives of atom and step economy. In this context, a variety of processes have been developed for the construction of synthetically and biologically important organic azides through the oxidative C–H bonds azidation. In this review, we have summarized recent progress in the direct azidation of C(sp(2))–H bonds. The review is divided into three major sections: (i) direct azidation of aromatic C–H bonds; (ii) direct azidation of olefinic C–H bonds; and (iii) direct azidation of aldehydic C–H bonds. Mechanistic aspects of the reactions are considered and discussed in detail. |
format | Online Article Text |
id | pubmed-9069887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90698872022-05-05 Methods for direct C(sp(2))–H bonds azidation Liu, Ying Ebadi, Abdol Ghaffar Youseftabar-Miri, Leila Hassanpour, Akbar Vessally, Esmail RSC Adv Chemistry Direct functionalization of C–H bonds has attracted great attention in recent years from the perspectives of atom and step economy. In this context, a variety of processes have been developed for the construction of synthetically and biologically important organic azides through the oxidative C–H bonds azidation. In this review, we have summarized recent progress in the direct azidation of C(sp(2))–H bonds. The review is divided into three major sections: (i) direct azidation of aromatic C–H bonds; (ii) direct azidation of olefinic C–H bonds; and (iii) direct azidation of aldehydic C–H bonds. Mechanistic aspects of the reactions are considered and discussed in detail. The Royal Society of Chemistry 2019-08-13 /pmc/articles/PMC9069887/ /pubmed/35528700 http://dx.doi.org/10.1039/c9ra04534a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Liu, Ying Ebadi, Abdol Ghaffar Youseftabar-Miri, Leila Hassanpour, Akbar Vessally, Esmail Methods for direct C(sp(2))–H bonds azidation |
title | Methods for direct C(sp(2))–H bonds azidation |
title_full | Methods for direct C(sp(2))–H bonds azidation |
title_fullStr | Methods for direct C(sp(2))–H bonds azidation |
title_full_unstemmed | Methods for direct C(sp(2))–H bonds azidation |
title_short | Methods for direct C(sp(2))–H bonds azidation |
title_sort | methods for direct c(sp(2))–h bonds azidation |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069887/ https://www.ncbi.nlm.nih.gov/pubmed/35528700 http://dx.doi.org/10.1039/c9ra04534a |
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