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The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water
The rapid and efficient KI/H(2)O(2)-mediated 2-sulfonylation of substituted indoles and N-methylpyrrole was established. The corresponding 2-sulfonylation products are synthesized from readily available sulfur sources, namely arylsulfonyl hydrazides, 4-methylbenzenesulfinic acid and sodium 4-methylb...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092009/ https://www.ncbi.nlm.nih.gov/pubmed/35559293 http://dx.doi.org/10.1039/c8ra09367a |
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author | Zhang, Jun Wang, Zhong Chen, Lingjuan Liu, Yan Liu, Ping Dai, Bin |
author_facet | Zhang, Jun Wang, Zhong Chen, Lingjuan Liu, Yan Liu, Ping Dai, Bin |
author_sort | Zhang, Jun |
collection | PubMed |
description | The rapid and efficient KI/H(2)O(2)-mediated 2-sulfonylation of substituted indoles and N-methylpyrrole was established. The corresponding 2-sulfonylation products are synthesized from readily available sulfur sources, namely arylsulfonyl hydrazides, 4-methylbenzenesulfinic acid and sodium 4-methylbenzenesulfinate in good to excellent yields in only 5 min. Moreover, the aqueous solution of hydrogen peroxide is used as both oxidant and solvent. Mechanistic studies demonstrated that 2,3-diiodoindoline was the main sulfonylation intermediate. |
format | Online Article Text |
id | pubmed-9092009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90920092022-05-11 The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water Zhang, Jun Wang, Zhong Chen, Lingjuan Liu, Yan Liu, Ping Dai, Bin RSC Adv Chemistry The rapid and efficient KI/H(2)O(2)-mediated 2-sulfonylation of substituted indoles and N-methylpyrrole was established. The corresponding 2-sulfonylation products are synthesized from readily available sulfur sources, namely arylsulfonyl hydrazides, 4-methylbenzenesulfinic acid and sodium 4-methylbenzenesulfinate in good to excellent yields in only 5 min. Moreover, the aqueous solution of hydrogen peroxide is used as both oxidant and solvent. Mechanistic studies demonstrated that 2,3-diiodoindoline was the main sulfonylation intermediate. The Royal Society of Chemistry 2018-12-12 /pmc/articles/PMC9092009/ /pubmed/35559293 http://dx.doi.org/10.1039/c8ra09367a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Zhang, Jun Wang, Zhong Chen, Lingjuan Liu, Yan Liu, Ping Dai, Bin The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water |
title | The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water |
title_full | The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water |
title_fullStr | The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water |
title_full_unstemmed | The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water |
title_short | The fast and efficient KI/H(2)O(2) mediated 2-sulfonylation of indoles and N-methylpyrrole in water |
title_sort | fast and efficient ki/h(2)o(2) mediated 2-sulfonylation of indoles and n-methylpyrrole in water |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092009/ https://www.ncbi.nlm.nih.gov/pubmed/35559293 http://dx.doi.org/10.1039/c8ra09367a |
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