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Enantiospecific Synthesis of Alkylboronate Esters Enabled by Carbopalladation of C─C σ-Bond and Novel Tsuji–Trost-Type Allylations

Enantiospecific Synthesis of Alkylboronate Esters Enabled by Carbopalladation of C─C σ-Bond and Novel Tsuji–Trost-Type Allylations
通过 CâC Ï 键的碳钯化和新型 TsujiâTrost 型烯丙基化实现烷基硼酸酯的对映特异性合成
批准号:
442129649
负责人:
Dr. Hui Wang
金额:
$0.0万
依托单位:
依托单位国家:
德国
项目类别:
Research Fellowships
财政年份:
2020
资助国家:
德国
项目状态:
已结题
起止时间:
2019-12-31 至 2021-12-31

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中文摘要
翻译
手性硼酸及其相关衍生物在立体选择性有机合成中是非常有价值的构件,因为它们可以经历大量的不对称转化。由于硼化学的巨大潜力,我们的目标是开发新的和不同的反应,使我们能够合成新的和有价值的手性硼化合物。Aggarwal基团在锂硼化反应和手性硼化合物及其天然产物的流水线合成方面取得了显着进展。Aggarwal等人通过C-Cσ-键的碳偶联(使用环-应变策略)进行的史无前例的远端交叉偶联反应。开辟了有机硼化学的新方向。在这一点上,开发一种高效的催化金属酸移位转化以使C-─C-σ-键在较不紧张的底物上发生碳转移是非常有必要的。同时,利用外消旋α-卤代烯丙基硼酸酯进行的Tsuji-Trost反应也为合成富含对映体的烷基硼酸酯提供了很好的机会。在这项研究中,我们将研究和设计更通用和更少应变的底物来实现催化的‘连接’交叉偶联,并合成广泛的外消旋α-卤代烯丙基硼酸酯,以实现与不同亲核试剂的Tsuji-Trost反应。我们预见,这些转化可以为构建用于不对称合成的手性烷基硼酸酯构筑块提供新的机会。
英文摘要
Chiral boronic acids and related derivatives are highly valuable building blocks in stereoselective organic synthesis because of the multitude of asymmetric transformations that they can undergo. Due to the tremendous potential of boron chemistry, our aim here is to develop new and different reactions that enable us to synthesize novel and valuable chiral boron-compounds. Aggarwal group has made remarkable progresses in lithiation-borylation and assembly-line synthesis of chiral boron-compounds and natural products. The unprecedented distal cross-coupling reaction via carbopalladation of C–C σ-bonds (using a ring-strain strategy) by Aggarwal et al. opens up a new direction in organoboron chemistry. In this regard, developing an efficient catalytic metalate-shift-based transformation to enable C─C σ-bond carbopalladation in less strained substrates is highly desirable. Meanwhile, the Tsuji-Trost reaction utilizing a racemic α-halo allyl boronic ester also provides great opportunities for the synthesis of enantioenriched alkyl boronate esters. In this research, we will investigate and design more general and less strained substrates to accomplish catalytic ‘conjunctive’ cross-couplings and synthesize a wide range of racemic α-halo allyl boronic esters to achieve Tsuji-Trost reactions with different nucleophiles. We envision that these transformations can provide new opportunities for the construction of chiral alkyl boronic ester building blocks for use in asymmetric synthesis.
期刊论文(2)
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国内基金
海外基金
新型滤波器综合技术-直接综合技术(Direct synthesis Technique)的研究及应用
  • 批准号:
    61671111
  • 项目类别:
    面上项目
  • 资助金额:
    58.0万元
  • 批准年份:
    2016
  • 负责人:
    肖飞
  • 依托单位: