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Recent Advances in Carbonylative Difunctionalization of Alkenes

Jin‐Bao Peng

2020Advanced Synthesis & Catalysis80 citationsDOI

Abstract

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

Topics & Concepts

CarbonylationChemistryStereocenterFunctional groupCombinatorial chemistrySubstrate (aquarium)NanotechnologyBiochemical engineeringOrganic chemistryCatalysisCarbon monoxideEnantioselective synthesisMaterials scienceOceanographyPolymerEngineeringGeologyCatalytic C–H Functionalization MethodsOxidative Organic Chemistry ReactionsCatalytic Cross-Coupling Reactions
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