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Sequential Catalytic Functionalization of Aryltriazenyl Aldehydes for the Synthesis of Complex Benzenes

Sangwon Seo, Ming Gao, Eva Paffenholz, Michael C. Willis

2021ACS Catalysis20 citationsDOIOpen Access PDF

Abstract

We demonstrate that aryltriazenes can promote three distinctive types of C-H functionalization reactions, allowing the preparation of complex benzene molecules with diverse substitution patterns. 2-Triazenylbenzaldehydes are shown to be efficient substrates for Rh(I)-catalyzed intermolecular alkyne hydroacylation reactions. The resulting triazene-substituted ketone products can then undergo either a Rh(III)-catalyzed C-H activation, or an electrophilic aromatic substitution reaction, achieving multifunctionalization of the benzene core. Subsequent triazene derivatization provides traceless products.

Topics & Concepts

TriazeneChemistryCatalysisHydroacylationKetoneAlkyneElectrophilic aromatic substitutionElectrophileSurface modificationDerivatizationBenzeneIntermolecular forceCombinatorial chemistryOrganic chemistryMoleculeAldehydeHigh-performance liquid chromatographyPhysical chemistryCatalytic C–H Functionalization MethodsCatalytic Cross-Coupling ReactionsRadical Photochemical Reactions
Sequential Catalytic Functionalization of Aryltriazenyl Aldehydes for the Synthesis of Complex Benzenes | Litcius