Litcius/Paper detail

Cleavage and Reassembly C≡C Bonds of Ynones to Access Highly Functionalized Ketones

Jiaxin Rong, Haowen Li, Rui Fu, Wangbin Sun, Teck‐Peng Loh, Yaojia Jiang

2020ACS Catalysis22 citationsDOI

Abstract

An economical strategy has been designed to formally cleave C≡C bonds of ynones through copper-catalyzed carbene chemistry. It proceeds under mild reaction conditions in a step-economy process by simultaneously cleaving the C≡C bonds and constructing C–C bonds. Depending on the substitution of the ynones, the reactions can proceed efficiently to generate synthetically useful 1,4-ketoaldehydes and cyclopentenone compounds. A plausible pathway is proposed that involves an active cyclopropane intermediate that consequently undergoes a cascade ring-opening reaction. The method works for a spectrum of ynones and N-tosylhydrazones that give good to excellent yields using a cheap copper catalytic system.

Topics & Concepts

ChemistryCleaveCyclopropaneCyclopentenoneCatalysisCarbeneBond cleavageCyclopropanationCombinatorial chemistryCopperRing (chemistry)Cleavage (geology)StereochemistryOrganic chemistryMaterials scienceComposite materialFracture (geology)EnzymeCyclopropane Reaction MechanismsCatalytic C–H Functionalization MethodsCatalytic Alkyne Reactions