Litcius/Paper detail

Iron-catalyzed tandem oxidative coupling and acetal hydrolysis reaction to prepare formylated benzothiazoles and isoquinolines

Yue Wu, Peng Guo, Long Chen, Weijie Duan, Zengzhuan Yang, Tao Wang, Ting Chen, Fei Xiong

2021Chemical Communications26 citationsDOI

Abstract

The aldehyde group is one of the most versatile intermediates in synthetic chemistry, and the introduction of an aldehyde group into heteroarenes is important for the transformation of molecular structure. Herein, we achieved the direct formylation of benzothiazo/les and isoquinolines. The reaction features a novel iron-catalyzed Minisci-type oxidative coupling process using commercially available 1,3-dioxolane as a formylated reagent followed by acetal hydrolysis without a separation process. The reaction can be performed under exceedingly mild reaction conditions and exhibits broad functional group tolerance.

Topics & Concepts

AldehydeChemistryAcetalCatalysisHydrolysisTandemOxidative coupling of methaneOxidative phosphorylationTransformation (genetics)Combinatorial chemistryOrganic chemistryMaterials scienceGeneBiochemistryComposite materialCatalytic C–H Functionalization MethodsOxidative Organic Chemistry ReactionsRadical Photochemical Reactions
Iron-catalyzed tandem oxidative coupling and acetal hydrolysis reaction to prepare formylated benzothiazoles and isoquinolines | Litcius