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Azidation in the Difunctionalization of Olefins
Organic azides are key motifs in compounds of relevance to chemical biology, medicinal chemistry and materials science. In addition, they also serve as useful building blocks due to their remarkable reactivity. Therefore, the development of efficient protocols to synthesize these compounds is of gre...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274056/ https://www.ncbi.nlm.nih.gov/pubmed/26999085 http://dx.doi.org/10.3390/molecules21030352 |
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author | Wu, Kai Liang, Yujie Jiao, Ning |
author_facet | Wu, Kai Liang, Yujie Jiao, Ning |
author_sort | Wu, Kai |
collection | PubMed |
description | Organic azides are key motifs in compounds of relevance to chemical biology, medicinal chemistry and materials science. In addition, they also serve as useful building blocks due to their remarkable reactivity. Therefore, the development of efficient protocols to synthesize these compounds is of great significance. This paper reviews the major applications and development of azidation in difunctionalization of olefins using azide reagents. |
format | Online Article Text |
id | pubmed-6274056 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62740562018-12-28 Azidation in the Difunctionalization of Olefins Wu, Kai Liang, Yujie Jiao, Ning Molecules Review Organic azides are key motifs in compounds of relevance to chemical biology, medicinal chemistry and materials science. In addition, they also serve as useful building blocks due to their remarkable reactivity. Therefore, the development of efficient protocols to synthesize these compounds is of great significance. This paper reviews the major applications and development of azidation in difunctionalization of olefins using azide reagents. MDPI 2016-03-16 /pmc/articles/PMC6274056/ /pubmed/26999085 http://dx.doi.org/10.3390/molecules21030352 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Wu, Kai Liang, Yujie Jiao, Ning Azidation in the Difunctionalization of Olefins |
title | Azidation in the Difunctionalization of Olefins |
title_full | Azidation in the Difunctionalization of Olefins |
title_fullStr | Azidation in the Difunctionalization of Olefins |
title_full_unstemmed | Azidation in the Difunctionalization of Olefins |
title_short | Azidation in the Difunctionalization of Olefins |
title_sort | azidation in the difunctionalization of olefins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274056/ https://www.ncbi.nlm.nih.gov/pubmed/26999085 http://dx.doi.org/10.3390/molecules21030352 |
work_keys_str_mv | AT wukai azidationinthedifunctionalizationofolefins AT liangyujie azidationinthedifunctionalizationofolefins AT jiaoning azidationinthedifunctionalizationofolefins |