羰基化
化学
立体中心
功能群
组合化学
基质(水族馆)
纳米技术
生化工程
有机化学
催化作用
一氧化碳
对映选择合成
工程类
材料科学
聚合物
地质学
海洋学
标识
DOI:10.1002/adsc.202000500
摘要
Abstract 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 β ‐substituted carbonyl compounds. The carbonylative difunctionalization of alkenes involves the formation of three σ ‐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. magnified image
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