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Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents

A green one-pot 2,3,6-trifunctionalization of N-alkyl/aryl indoles was achieved by adding three equivalents of N-Br sulfoximine to the indole solution. A variety of 2-sulfoximidoyl-3,6-dibromo indoles were prepared with 38–94% yields using N-Br sulfoximines as both brominating and sulfoximinating re...

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Autores principales: Chen, Xiao Yun, Tang, Yaonan, Xiang, Xinran, Tang, Yisong, Huang, Mingyang, Zheng, Shaojun, Yang, Cuifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146707/
https://www.ncbi.nlm.nih.gov/pubmed/37110617
http://dx.doi.org/10.3390/molecules28083380
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author Chen, Xiao Yun
Tang, Yaonan
Xiang, Xinran
Tang, Yisong
Huang, Mingyang
Zheng, Shaojun
Yang, Cuifeng
author_facet Chen, Xiao Yun
Tang, Yaonan
Xiang, Xinran
Tang, Yisong
Huang, Mingyang
Zheng, Shaojun
Yang, Cuifeng
author_sort Chen, Xiao Yun
collection PubMed
description A green one-pot 2,3,6-trifunctionalization of N-alkyl/aryl indoles was achieved by adding three equivalents of N-Br sulfoximine to the indole solution. A variety of 2-sulfoximidoyl-3,6-dibromo indoles were prepared with 38–94% yields using N-Br sulfoximines as both brominating and sulfoximinating reagents. Based on the results of controlled experiments, we propose that a radical substitution involving 3,6-dibromination and 2-sulfoximination occurs in the reaction process. This is first time that 2,3,6-trifunctionalization of indole in one pot has been achieved.
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spelling pubmed-101467072023-04-29 Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents Chen, Xiao Yun Tang, Yaonan Xiang, Xinran Tang, Yisong Huang, Mingyang Zheng, Shaojun Yang, Cuifeng Molecules Article A green one-pot 2,3,6-trifunctionalization of N-alkyl/aryl indoles was achieved by adding three equivalents of N-Br sulfoximine to the indole solution. A variety of 2-sulfoximidoyl-3,6-dibromo indoles were prepared with 38–94% yields using N-Br sulfoximines as both brominating and sulfoximinating reagents. Based on the results of controlled experiments, we propose that a radical substitution involving 3,6-dibromination and 2-sulfoximination occurs in the reaction process. This is first time that 2,3,6-trifunctionalization of indole in one pot has been achieved. MDPI 2023-04-11 /pmc/articles/PMC10146707/ /pubmed/37110617 http://dx.doi.org/10.3390/molecules28083380 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Xiao Yun
Tang, Yaonan
Xiang, Xinran
Tang, Yisong
Huang, Mingyang
Zheng, Shaojun
Yang, Cuifeng
Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
title Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
title_full Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
title_fullStr Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
title_full_unstemmed Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
title_short Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents
title_sort green one-pot syntheses of 2-sulfoximidoyl-3,6-dibromo indoles using n-br sulfoximines as both brominating and sulfoximinating reagents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146707/
https://www.ncbi.nlm.nih.gov/pubmed/37110617
http://dx.doi.org/10.3390/molecules28083380
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