Difluorocarbene-Mediated Trimethylsilylation of Nucleophiles with HCF2N(TMS)2 as a Silylation Reagent

IF 5 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2025-02-10 DOI:10.1021/acs.orglett.5c00227
Hao Ruan, Dong Zhu, Jingwei Zhao, Shifa Zhu
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Abstract

Described herein is the trimethylsilylation of various nucleophiles using a combination of HCF3 and NaHMDS. This facile protocol enables the rapid construction of alkynylsilanes, silyl enol ethers, etc., under mild conditions. Detailed mechanistic studies indicate that the trimethylsilicon intermediate formed in situ can be readily attacked by nucleophiles, with the activation of the base NaHMDS by difluorocarbene. This work first utilizes the structure of HMDS as a silicon source in the trimethylsilylation of terminal alkynes.

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HCF2N(TMS)2作为硅化试剂介导的亲核试剂三甲基硅化反应
本文描述的是使用HCF3和NaHMDS的组合对各种亲核试剂进行三甲基硅基化。这种简单的协议使得在温和的条件下快速构建炔基硅烷,硅烯醇醚等。详细的机理研究表明,原位形成的三甲基硅中间体很容易受到亲核试剂的攻击,碱NaHMDS被二氟烃激活。本研究首次利用HMDS结构作为末端炔三甲基硅化反应的硅源。
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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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