Palladium-Catalyzed Domino Conversion of Aryl–Thianthreniums with Anhydrides: Rapidly Building Highly Functionalized Fluorenones

IF 5 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-04-15 DOI:10.1021/acs.orglett.4c00302
Jiang Nan*, Haiyan Xiao, Yangmin Ma, Liangxin Fan* and Jing Wang*, 
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Abstract

As a class of rising electrophilic coupling reagents, aryl–thianthreniums (aryl-TTs) have been gaining immense attention. Herein, a novel palladium-catalyzed domino annulation of aryl-TTs with anhydrides is proposed to rapidly assemble a collection of highly functionalized fluorenones. This finding presents an innovative reaction pattern of aryl-TTs wherein the domino annulation version is first involved. Heavily compared with the existing conversions with aryl-TTs, this identified process successively functions as four aryl C–H bonds.

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钯催化芳基噻蒽与酸酐的多米诺转化:快速构建高官能度的芴酮类化合物
作为一类新兴的亲电偶联试剂,芳基噻蒽(arryl-TTs)一直备受关注。本文提出了一种新型钯催化多米诺环化芳基-TTs 与酸酐的反应,可快速组装出一系列高官能度的芴酮。这一发现提出了一种创新的芳基-TTs 反应模式,其中首先涉及多米诺环化版本。与现有的芳基-TTs 转化相比,这一已确定的过程连续起到四个芳基 C-H 键的作用。
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来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
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