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Recent Advances in Carbonylative Difunctionalization of Alkenes

机译:烯基的羰基化双官能化的最新进展

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摘要

The carbonylation reaction represents one of the most powerful methods for the rapid build-up of carbonyl structures and has widely applied in both academic and industry fields. Carbonylative difunctionalization of alkenes, which installs a unique functional group and a carbonyl group across the C-C double bonds, offers a high potential strategy for the selective synthesis of beta-substituted carbonyl compounds. The carbonylative difunctionalization of alkenes involves the formation of three sigma-bonds and two stereocenters as well as a carbonyl group in a single transformation. Careful design of the substrate and control of reaction pathway would result unexpected advantages in constructing complex structures, which are ubiquitous in natural products, pharmaceuticals and functional materials. In this Review, the important advances and contributions in carbonylative difunctionalization of alkenes are summarized based on the different reaction types, with the wish to inspire future studies and promote further developments in this field.
机译:羰基化反应是羰基结构快速积聚的最强大方法之一,并且在学术界和工业领域广泛应用。在C-C双键上安装独特的官能团和羰基的羰基双官能化提供了对选择性合成β取代的羰基化合物的高潜在策略。烯基的羰基化双官能化涉及形成三个σ-键和两个立体封闭剂以及单一转化中的羰基。仔细设计基材和反应途径的控制会导致构建复杂结构方面的意外优点,这在天然产物,药物和功能材料中普遍存在。在本文中,基于不同的反应类型,总结了烯基双核化化的重要进展和贡献,希望激励未来的研究,促进该领域的进一步发展。

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