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Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin

Sanliang Li, Qiaoyu Chen, Zhan‐Ming Zhang, Junliang Zhang

2021Green Synthesis and Catalysis28 citationsDOIOpen Access PDF

Abstract

A first palladium-catalyzed asymmetric intramolecular Heck reaction for the construction 3,4-dihydro-1-(2H)-isoquinolinone containing the quaternary carbon chiral center has been developed. The salient features of this reaction include high efficiency, high enantioselectivity, the novel chiral ligand and diverse transformations.

Topics & Concepts

Enantioselective synthesisIntramolecular forceOlefin fiberCatalysisHeck reactionChemistryQuaternary carbonPalladiumLigand (biochemistry)Combinatorial chemistryStereochemistryMedicinal chemistryOrganic chemistryReceptorBiochemistryCatalytic Cross-Coupling ReactionsChemical synthesis and alkaloidsCatalytic C–H Functionalization Methods
Pd-catalyzed enantioselective intramolecular Heck reaction to access disubstituted dihydroisoquinolinone with a terminal olefin | Litcius