PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines

A PIDA mediated intramolecular oxidative C–N coupling and subsequent detosylative aromatization to afford indolo[2,3-b]quinoline derivatives has been developed. This tandem reaction provided an efficient method for the synthesis of valuable indolo[2,3-b]quinoline derivatives.

Detalles Bibliográficos
Autores principales: Wang, Quan-Bing, Tang, Shi, Wang, Ying-Jie, Yuan, Yue, Chen, Tieqiao, Jia, Ai-Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032537/
https://www.ncbi.nlm.nih.gov/pubmed/35479722
http://dx.doi.org/10.1039/d1ra01894a
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author Wang, Quan-Bing
Tang, Shi
Wang, Ying-Jie
Yuan, Yue
Chen, Tieqiao
Jia, Ai-Qun
author_facet Wang, Quan-Bing
Tang, Shi
Wang, Ying-Jie
Yuan, Yue
Chen, Tieqiao
Jia, Ai-Qun
author_sort Wang, Quan-Bing
collection PubMed
description A PIDA mediated intramolecular oxidative C–N coupling and subsequent detosylative aromatization to afford indolo[2,3-b]quinoline derivatives has been developed. This tandem reaction provided an efficient method for the synthesis of valuable indolo[2,3-b]quinoline derivatives.
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spelling pubmed-90325372022-04-26 PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines Wang, Quan-Bing Tang, Shi Wang, Ying-Jie Yuan, Yue Chen, Tieqiao Jia, Ai-Qun RSC Adv Chemistry A PIDA mediated intramolecular oxidative C–N coupling and subsequent detosylative aromatization to afford indolo[2,3-b]quinoline derivatives has been developed. This tandem reaction provided an efficient method for the synthesis of valuable indolo[2,3-b]quinoline derivatives. The Royal Society of Chemistry 2021-05-10 /pmc/articles/PMC9032537/ /pubmed/35479722 http://dx.doi.org/10.1039/d1ra01894a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Wang, Quan-Bing
Tang, Shi
Wang, Ying-Jie
Yuan, Yue
Chen, Tieqiao
Jia, Ai-Qun
PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
title PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
title_full PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
title_fullStr PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
title_full_unstemmed PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
title_short PhI(OAc)(2)-mediated intramolecular oxidative C–N coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
title_sort phi(oac)(2)-mediated intramolecular oxidative c–n coupling and detosylative aromatization: an access to indolo[2,3-b]quinolines
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032537/
https://www.ncbi.nlm.nih.gov/pubmed/35479722
http://dx.doi.org/10.1039/d1ra01894a
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