Photogeneration of β-Borylsilyl Radical via Decarboxylation of N-Hydroxyphthalimide Esters

IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-10-16 DOI:10.1021/acs.orglett.4c03393
Guotao Lin, Yu Guo, Mengjie Zhang, Qingqing Xuan, Jian Xu, Qiuling Song
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Abstract

Gem-borylsilylalkanes are versatile intermediates in organic synthesis, and the traditional synthesis methods have mainly focused on metal reagents, the insertion reactions of diazo compounds, and hydrosilylation/hydroborylation reactions of unsaturated bonds. Herein, a novel, efficient gem-borylsilylalkanes synthesis via a radical approach is reported. This method introduced a β-gem-borylsilyl NHPI ester as the precursor of the β-borylsilyl radical that, coupling with radical acceptors under photo conditions, and the corresponding gem-borylsilylalkanes bearing unsaturated bonds, facilitate subsequent transformations.

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通过 N-羟基邻苯二甲酰亚胺酯的脱羧作用光生成 β-鲍里硅基自由基
宝石酰硅烷是有机合成中用途广泛的中间体,传统的合成方法主要集中在金属试剂、重氮化合物的插入反应以及不饱和键的氢化/氢化反应等方面。本文报告了一种通过自由基方法合成新颖、高效的 gem-borylsilylalkanes 的方法。该方法引入了一种 β-金银烷基 NHPI 酯作为 β-金银烷基自由基的前体,在光照条件下与自由基受体偶联,生成相应的含不饱和键的金银烷烃,从而促进了后续转化。
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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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