Litcius/Paper detail

Carbon-Chain Elongation by Co-Catalyzed Selective C–C Bond Cleavage and Subsequent Silylperoxylation of Alkene Substrates

Jiahao Xie, Terumasa Kato, Keiji Maruoka

2024ACS Catalysis6 citationsDOI

Abstract

A Co-catalyzed selective C–C bond cleavage followed by the silylperoxylation of alkene substrates generated a series of alkylsilyl peroxides with good yields and selectivities. Further transformation through transition-metal-catalyzed cleavage of the resulting alkylsilyl peroxides and subsequent functionalization with coupling partners could generate a series of dicarbonyl compounds. This two-step transformation was carried out in a one-pot manner, which enhances the practicability of this approach. A plausible reaction mechanism was proposed to interpret the C–C bond cleavage and subsequent silylperoxylation of the alkene substrates.

Topics & Concepts

AlkeneCatalysisChemistryCleavage (geology)Bond cleavageCarbon fibersElongationPhotochemistryOrganic chemistryStereochemistryPolymer chemistryMaterials scienceComposite materialComposite numberUltimate tensile strengthMetallurgyFracture (geology)Oxidative Organic Chemistry ReactionsCatalytic C–H Functionalization MethodsSynthetic Organic Chemistry Methods
Carbon-Chain Elongation by Co-Catalyzed Selective C–C Bond Cleavage and Subsequent Silylperoxylation of Alkene Substrates | Litcius