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Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles
Arenesulfonyl indoles, bearing a good leaving group, are effective precursors for vinylogous imine intermediates which are generated in situ under basic conditions. This intermediate can readily react with other nucleophilic reagents to obtain C-3 substituted indole derivatives. In the last few year...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693840/ https://www.ncbi.nlm.nih.gov/pubmed/35424187 http://dx.doi.org/10.1039/d0ra09133b |
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author | Kaur, Banni Preet Kaur, Jasneet Chimni, Swapandeep Singh |
author_facet | Kaur, Banni Preet Kaur, Jasneet Chimni, Swapandeep Singh |
author_sort | Kaur, Banni Preet |
collection | PubMed |
description | Arenesulfonyl indoles, bearing a good leaving group, are effective precursors for vinylogous imine intermediates which are generated in situ under basic conditions. This intermediate can readily react with other nucleophilic reagents to obtain C-3 substituted indole derivatives. In the last few years, a plethora of exciting synthetic applications of this substrate have been exploited. The stability of arylsulfonyl-containing substrates, mild reaction conditions, and the large variety of nucleophiles involved in these procedures are the key to their success in organic synthesis. |
format | Online Article Text |
id | pubmed-8693840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86938402022-04-13 Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles Kaur, Banni Preet Kaur, Jasneet Chimni, Swapandeep Singh RSC Adv Chemistry Arenesulfonyl indoles, bearing a good leaving group, are effective precursors for vinylogous imine intermediates which are generated in situ under basic conditions. This intermediate can readily react with other nucleophilic reagents to obtain C-3 substituted indole derivatives. In the last few years, a plethora of exciting synthetic applications of this substrate have been exploited. The stability of arylsulfonyl-containing substrates, mild reaction conditions, and the large variety of nucleophiles involved in these procedures are the key to their success in organic synthesis. The Royal Society of Chemistry 2021-01-08 /pmc/articles/PMC8693840/ /pubmed/35424187 http://dx.doi.org/10.1039/d0ra09133b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Kaur, Banni Preet Kaur, Jasneet Chimni, Swapandeep Singh Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles |
title | Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles |
title_full | Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles |
title_fullStr | Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles |
title_full_unstemmed | Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles |
title_short | Arenesulfonyl indole: new precursor for diversification of C-3 functionalized indoles |
title_sort | arenesulfonyl indole: new precursor for diversification of c-3 functionalized indoles |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693840/ https://www.ncbi.nlm.nih.gov/pubmed/35424187 http://dx.doi.org/10.1039/d0ra09133b |
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