Highly efficient construction of 2,3-disubstituted indoline derivatives by [4 + 1] annulation of sulfur ylides and o -sulfonamido aldimines

Herein, it is reported that a formal [4 + 1] cycloaddition of o -sulfonamido aldimines and sulfur ylides has been successfully developed. This strategy led to a series of 2,3-disubstituted indoline derivatives with synthetical flexible carbonyl and sulfamide groups obtained with good yields and high...

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Veröffentlicht in:Organic Chemistry Frontiers 2023-03, Vol.10 (6), p.1521-1526
Hauptverfasser: Xu, Mengjiao, You, Mengwei, Su, Yang, Lu, Boxue Ruan, Liu, Ling, Lv, Xin, Wang, Shoulei, Mao, Hui, Zhou, Liejin
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container_issue 6
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container_title Organic Chemistry Frontiers
container_volume 10
creator Xu, Mengjiao
You, Mengwei
Su, Yang
Lu, Boxue Ruan
Liu, Ling
Lv, Xin
Wang, Shoulei
Mao, Hui
Zhou, Liejin
description Herein, it is reported that a formal [4 + 1] cycloaddition of o -sulfonamido aldimines and sulfur ylides has been successfully developed. This strategy led to a series of 2,3-disubstituted indoline derivatives with synthetical flexible carbonyl and sulfamide groups obtained with good yields and high diastereoselectivities. A variety of functional groups were well tolerated. It is worth noting that indoles could also be synthesized using this highly efficient cascade reaction.
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source Royal Society Of Chemistry Journals 2008-
subjects Carbonyl compounds
Carbonyls
Cascade chemical reactions
Chemical reactions
Cycloaddition
Functional groups
Indoles
Organic chemistry
Sulfamide
Sulfur
title Highly efficient construction of 2,3-disubstituted indoline derivatives by [4 + 1] annulation of sulfur ylides and o -sulfonamido aldimines
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