Ag-Catalyzed Selective C-C Bond Activation of Cyclopropenones to Access α-Alkylidene Lactones.

IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-07-26 Epub Date: 2024-07-11 DOI:10.1021/acs.orglett.4c01853
Shu-Lin Zhang, Zhao-Bing Wu, Chun-Xin Zhao, Yu-Xin Bai, Wei Sun, Meng Sun
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Abstract

A novel Ag-catalyzed ring opening of unsymmetric cyclopropenones for the stereoselective synthesis of a diverse range of α-alkylidene lactones has been developed. In this protocol, two different C-C(O) bonds were distinguished, demonstrating selective C-C bond activation. This reaction features a wide substrate scope, good functional group compatibility, and high atom economy, providing a versatile and general approach to the construction of α-alkylidene lactones.

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Ag 催化环丙烯酮的选择性 C-C 键活化以获得 α-亚烷基内酯。
我们开发了一种新型的 Ag 催化不对称环丙烯酮开环方法,用于立体选择性合成多种 α-亚烷基内酯。在该方案中,两个不同的 C-C(O)键被区分开来,证明了 C-C 键活化的选择性。该反应具有底物范围广、官能团兼容性好和原子经济性高等特点,为构建α-亚烷基内酯提供了一种通用的方法。
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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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