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Enabling the Cross-Coupling of Tertiary Organoboron Nucleophiles through Radical-Mediated Alkyl Transfer

机译:通过自由基介导的烷基转移实现叔有机器官亲核分子的交叉偶联

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摘要

The construction of quaternary centers is a common challenge in the synthesis of complex materials and natural products. Current cross-coupling strategies that can be generalized for setting these centers are sparse and, when known, are typically predicated on the use of reactive organometallic reagents. To address this shortcoming a new, photoredox-Ni dual catalytic strategy for the cross-coupling of tertiary organoboron reagents with aryl halides is reported. In addition to details on the cross-coupling scope and limitations, full screening efforts and mechanistic experiments are communicated.
机译:在复杂材料和天然产物的合成中,四元中心的建设是一个共同的挑战。可以概括用于设置这些中心的当前交叉偶联策略是稀疏的,并且,当已知时,通常以反应性有机金属试剂的使用为前提。为了解决该缺点,报道了用于叔有机硼试剂与芳基卤化物的交叉偶联的新的光氧化还原-Ni双重催化策略。除了交叉耦合范围和限制的详细信息外,还进行了全面的筛选工作和机理实验。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2017年第29期|9847-9850|共4页
  • 作者单位

    Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, PA, United States;

    Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, PA, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 03:08:01

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