Rhodium/Selenium Dual Catalysis for Accessing 2-Aminopyrroles from N-Sulfonyl-1,2,3-triazoles

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-01-23 DOI:10.1039/d4cc06346e
Chandra Volla, Kuntal Pal, Om Prakash Dash
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Abstract

Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(II)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.
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铑/硒双催化从n -磺酰基-1,2,3-三唑中获得2-氨基吡咯
本文报道了一种新的铑/硒双催化工艺,用于n -磺酰基-1,2,3-三唑合成2-氨基吡咯。所提出的协同催化机制包括:Rh(II)催化三唑生成Rh-azavinyl卡苯,然后硒催化生成ylide,随后与另一个Rh-azavinyl卡苯环合。简单温和的双催化策略可容纳多种吸电子和给电子官能团,以中高收率提供各种2-氨基吡咯衍生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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