tBuOK/TMSOK 介导的 "烷基卤化物到烷基自由基 "转化,用于无过渡金属安息香 α-C-H 烷基化反应

IF 5.5 1区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chinese Journal of Chemistry Pub Date : 2024-07-30 DOI:10.1002/cjoc.202400664
Zhouying Wang, Lu Gan, Zhibin Song, Yunyun Liu, Jie-Ping Wan
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引用次数: 0

摘要

综合摘要碱叔丁氧基(tBuOK 或 tBuONa)介导的芳基碘化物生成芳基自由基是自由基化学领域的一个里程碑式的发现。然而,类似的 "烷基卤化物到烷基自由基 "的转化尚未通过类似的催化策略在实际合成中实现。本文介绍了 tBuOK 或 TMSOK 在安息香的直接 α-C-H 烷基化过程中介导的首次实用的 "烷基卤化物到烷基自由基 "转化。与芳基自由基的生成同样重要的是,目前的研究工作为合成各种安息香类化合物提供了一种相当简便、有用的新方法,同时也是基于烷基自由基的合成中的重要一步,展示了简单碱基介导自由基形成的更高通用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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tBuOK/TMSOK-Mediated “Alkyl Halide to Alkyl Free Radical” Transformation for Transition-Metal-Free Benzoin α-C—H Alkylation

The alkali tert-butoxide (tBuOK or tBuONa) mediated generation of aryl free radical from aryl iodide remarks a milestone discovery in the free radical chemistry. However, the equivalent “alkyl halide to alkyl free radical” transformation has not yet been realized in applicable synthesis by similar catalytic tactic. In this paper, the first practical “alkyl halide to alkyl free radical” transformation mediated by tBuOK or TMSOK in the direct α-C—H alkylation of benzoins is presented. As the parallelly significant issue as aryl free radical generation, the current work, while bringing a rather facile and useful new approach for the synthesis of diverse benzoins, represents also an important step in the alkyl free radical-based synthesis by displaying the higher generality of simple alkali base mediated radical formation.

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来源期刊
Chinese Journal of Chemistry
Chinese Journal of Chemistry 化学-化学综合
CiteScore
8.80
自引率
14.80%
发文量
422
审稿时长
1.7 months
期刊介绍: The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.
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