Recent Advances in Carbonylative Difunctionalization of Alkenes

被引:61
|
作者
Peng, Jin-Bao [1 ]
机构
[1] Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
carbonylative difunctionalization; beta-substituted carbonyl; unactivated alkenes; multicomponent reaction; PALLADIUM-CATALYZED CYCLIZATION; ENANTIOSELECTIVE BIS-ALKOXYCARBONYLATION; ASYMMETRIC BIS(ALKOXYCARBONYLATION) REACTION; INTRAMOLECULAR HECK REACTION; CARBON-MONOXIDE; COUPLING REACTIONS; UNACTIVATED OLEFINS; SELECTIVE SYNTHESIS; CASCADE REACTIONS; METAL CATALYSIS;
D O I
10.1002/adsc.202000500
中图分类号
O69 [应用化学];
学科分类号
081704 ;
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.
引用
收藏
页码:3059 / 3080
页数:22
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