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Tin-Free Radical Carbon-Carbon Bond-Forming Reactions Based on alpha-Scission of Alkylsulfonyl Radicals

机译:基于烷基磺酰基的α-ScOS - 自由基碳 - 碳键 - 形成反应

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摘要

Tin-free radical reactions based on alpha-scission of alkylsulfonyl radicals are very useful for the formation of carbon-carbon bonds and include allylation, acylation, cyanation, vinylation, and carbonylation. For secondary, tertiary, and benzylic radicals, it is possible to use the corresponding iodides as precursors but the primary radicals still require the use of phenyl tellurides or alkyl allyl sulfones. Especially, alkyl allyl sulfones are highly efficient and most reliable primary alkyl radical precursors for the further formation of carbon-carbon bonds. The present approach is very useful for introducing various functional groups such as carbonyl and alkenyl groups under tin-free conditions.
机译:基于α-rOUncons的甲酸氨基分泌的无酸的自由基反应对于形成碳 - 碳键,并包括烯丙基化,酰化,氰化,乙烯化和羰基化。 对于次级,三级和苄基自由基,可以使用相应的碘化物作为前体,但主要基团仍然需要使用苯基碲化物或烷基烯丙基砜。 特别是,烷基烯丙基砜是高效且最可靠的初级烷基基质前体,用于进一步形成碳键。 本方法对于在无锡条件下将各种官能团如羰基和链烯基引入诸如羰基和链烯基的方法非常有用。

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  • 作者

    Sunggak Kim; Sangmo Kim;

  • 作者单位

    Center for Molecular Design &

    Synthesis and Department of Chemistry School of Molecular Science Korea Advanced Institute of Science and Technology Daejeon 305-701 Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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