Rh(III)-Catalyzed Imidoyl C-H Bond Activation/[4 + 2] Annulation of N-Benzimidazole Imines with Iodonium Ylides.

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Xiang Li,Qin Zhang,Xin Zheng
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引用次数: 0

Abstract

A general protocol for the synthesis of polycyclic benzo[4,5]imidazo[1,2-a]pyrimidines via Rh(III)-catalyzed imidoyl C-H bond activation of N-benzimidazole imines with iodonium ylides has been disclosed. This method features mild conditions, a broad substrate scope, and excellent functional group tolerance. Moreover, the reaction could be easily scaled up and was amendable with the in situ generated iodonium ylides, which demonstrated the practicality of this method.
Rh(III)催化n -苯并咪唑亚胺与碘酰亚胺的[4 + 2]环化。
通过Rh(III)催化n -苯并咪唑亚胺与碘基酰化反应,合成多环苯并[4,5]咪唑[1,2- A]嘧啶的一般方案。该方法具有条件温和,底物范围广,功能基团耐受性好等特点。此外,该反应易于扩大规模,并且可以用原位生成的碘化物进行修饰,证明了该方法的实用性。
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
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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