钴催化苯酰胺与烯基甲醇醋酸酯的区域选择性(4+2)环化:获得3-乙烯基异喹啉酮

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Chandra Volla, Pravin Kumar, Om Prakash Dash
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引用次数: 0

摘要

在此,我们揭示了一种共催化的区域选择性(4+2)环化芳基,异芳基和丙烯酰胺与醋酸丙烯酯的环化,以高收率获得各种各样的杂环衍生物,具有优异的区域选择性。该方案采用廉价的钴(II)盐,并具有广泛的官能团耐受性。溶剂在控制区域选择性迁移插入中起着至关重要的作用,促进了难以捉摸的共烯基中间体的选择性形成。进行了初步的机理实验来阐明可能的反应途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cobalt-Catalyzed Regioselective (4+2)-Annulation of Benzamides with Allenyl Carbinol Acetates: Access to 3-Vinylisoquinolinones
Herein we disclose a Co-catalyzed regioselective (4+2)annulation of aryl-, heteroaryl-and acrylamides with allenyl acetates to access a diverse array of heterocyclic derivatives in high yields with excellent regioselectivity. The protocol employs inexpensive cobalt(II) salts and exhibits broad functional group tolerance. Solvent plays a crucial role in governing regioselective migratory insertion, facilitating the selective formation of elusive Co-alkenyl intermediate. Preliminary mechanistic experiments were performed to elucidate the plausible reaction pathway.
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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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