Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation

Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation

Dearomatisation of indoles allows efficient access to indolines, but often is incompatible with electron-withdrawing substituents. Here a photoredox Giese-type dearomatisation of indoles yields 2,3-disubstituted indolines bearing electron-withdrawing groups.

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Autores principales: Yueteng Zhang, Peng Ji, Feng Gao, Yue Dong, He Huang, Changqing Wang, Ziyuan Zhou, Wei Wang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Chemistry
QD1-999
Acceso en línea:https://doaj.org/article/da92875c82464498980d218767a5bec9
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spelling oai:doaj.org-article:da92875c82464498980d218767a5bec92021-12-02T10:52:39ZOrganophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation10.1038/s42004-021-00460-y2399-3669https://doaj.org/article/da92875c82464498980d218767a5bec92021-02-01T00:00:00Zhttps://doi.org/10.1038/s42004-021-00460-yhttps://doaj.org/toc/2399-3669Dearomatisation of indoles allows efficient access to indolines, but often is incompatible with electron-withdrawing substituents. Here a photoredox Giese-type dearomatisation of indoles yields 2,3-disubstituted indolines bearing electron-withdrawing groups.Yueteng ZhangPeng JiFeng GaoYue DongHe HuangChangqing WangZiyuan ZhouWei WangNature PortfolioarticleChemistryQD1-999ENCommunications Chemistry, Vol 4, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Chemistry
QD1-999
spellingShingle Chemistry
QD1-999
Yueteng Zhang
Peng Ji
Feng Gao
Yue Dong
He Huang
Changqing Wang
Ziyuan Zhou
Wei Wang
Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation
description Dearomatisation of indoles allows efficient access to indolines, but often is incompatible with electron-withdrawing substituents. Here a photoredox Giese-type dearomatisation of indoles yields 2,3-disubstituted indolines bearing electron-withdrawing groups.
format article
author Yueteng Zhang
Peng Ji
Feng Gao
Yue Dong
He Huang
Changqing Wang
Ziyuan Zhou
Wei Wang
author_facet Yueteng Zhang
Peng Ji
Feng Gao
Yue Dong
He Huang
Changqing Wang
Ziyuan Zhou
Wei Wang
author_sort Yueteng Zhang
title Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation
title_short Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation
title_full Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation
title_fullStr Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation
title_full_unstemmed Organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a Giese-type transformation
title_sort organophotocatalytic dearomatization of indoles, pyrroles and benzo(thio)furans via a giese-type transformation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/da92875c82464498980d218767a5bec9
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