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Recent Advances in the Activation of Boron and Silicon Reagents for Stereocontrolled Allylation Reactions

机译:立体控制烯丙基化反应中硼和硅试剂活化的最新进展

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Despite the popularity of boron and silicon allylation reagents in stereocontrolled synthesis, they suffer from a number of inherent limitations that have slowed down their development as synthetic tools for nucleophilic additions to carbonyl compounds and imine derivatives. These limitations are the low reactivity and diastereoselectivity of allyl trialkylsilane reagents, and the lack of catalytic systems for the activation and substoichiometric control of enantioselectivity in the additions of allyl boron reagents. To develop more efficient and general methods for the control of absolute stereochemistry in the resulting homoallylic alcohols, new approaches aimed at solving the problem of activation of allylic boron and silicon reagents are needed. This Minireview describes a number of recent approaches that have been devised to address this problem.
机译:尽管硼和硅烯丙基化试剂在立体控制的合成中很受欢迎,但它们仍遭受许多固有的局限性,这些局限性使其作为羰基化合物和亚胺衍生物进行亲核加成的合成工具的发展减慢了速度。这些限制是烯丙基三烷基硅烷试剂的低反应性和非对映选择性,以及在添加烯丙基硼试剂中缺少用于活化和亚化学计量控制对映选择性的催化体系。为了开发用于控制所得均烯丙基醇中的绝对立体化学的更有效和通用的方法,需要旨在解决烯丙基硼和硅试剂的活化问题的新方法。此Minireview描述了为解决此问题而设计的许多最新方法。

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