Synthesis of Polycyclic Imidazoles via α-C-H/N-H Annulation of Alicyclic Amines.

IF 2.2 4区 化学 Q2 CHEMISTRY, ORGANIC
Synthesis-Stuttgart Pub Date : 2023-08-01 Epub Date: 2023-04-13 DOI:10.1055/a-2022-1511
Subhradeep Dutta, Kamal Bhatt, Fabian Cuffel, Daniel Seidel
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引用次数: 0

Abstract

Secondary alicyclic amines are converted to their corresponding ring-fused imidazoles in a simple procedure consisting of oxidative imine formation followed by a van Leusen reaction. Amines with an existing α-substituent undergo regioselective ring-fusion at the α'-position. This method was utilized in a synthesis of fadrozole.

通过脂环胺的α-C-H/N-H 嵌合合成多环咪唑。
仲脂环胺可以通过一个简单的过程转化为相应的环融合咪唑,该过程包括氧化亚胺形成和范-莱森反应。带有 α 取代基的胺在α'-位发生区域选择性环融合。这种方法被用于合成法卓唑。
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
Synthesis-Stuttgart
Synthesis-Stuttgart 化学-有机化学
CiteScore
4.50
自引率
7.70%
发文量
435
审稿时长
1 months
期刊介绍: SYNTHESIS is an international full-paper journal devoted to the advancement of the science of chemical synthesis. It covers all fields of organic chemistry involving synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines. SYNTHESIS provides dependable research results with detailed and reliable experimental procedures and full characterization of all important new products as well as scientific primary data.
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