Photoredox-Catalyzed Multicomponent α-Sulfonylation of Terminal Alkynes

IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-11-11 DOI:10.1021/acs.orglett.4c03828
Mingyue Zheng, Xin Zhuang, Qianfa Jia, Qiao Ren, Jicheng Wu
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Abstract

A generality-oriented and adaptive α-sulfonylation of alkynes via photoinduced multicomponent radical cross-coupling of terminal alkynes with sulfinates and a variety of alcohols, thiophenols, or selenophenols has been explored. This protocol features mild conditions, good functional group tolerability, broad substrate scope, excellent chemo-, site-, and stereoselectivity, and applicability to late-stage functionalization. It provides a modular platform for the synthesis of value-added structurally diverse α-sulfonyl-containing multisubstituted alkenes from simple precursors.

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光氧化催化多组分末端炔烃的 α 磺化反应
通过光诱导末端炔烃与硫酸盐和各种醇、噻吩酚或硒酚的多组分自由基交叉偶联,探索了一种面向通用性和适应性的炔烃α-磺酰化反应。该方案具有条件温和、官能团耐受性好、底物范围广、化学、位点和立体选择性优异以及适用于后期官能化等特点。它为从简单的前体合成结构多样化的高附加值 α-砜基多取代烯烃提供了一个模块化平台。
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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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