Redox‐Divergent Synthesis of Fluoroalkylated Pyridines and 2‐Pyridones through Cu‐Catalyzed N−O Cleavage of Oxime Acetates
作者:Dachang Bai、Xueli Wang、Guangfan Zheng、Xingwei Li
DOI:10.1002/anie.201802311
日期:2018.5.28
Cu‐catalyzed redox‐divergent [3+3] coupling of oxime esters with β‐CF3 enones and acrylates is described. This redox‐neutral coupling with enones and acrylates affords trifluoromethylated pyridines and pyridones, respectively. Under reductive conditions, difluoromethylated pyridines, difluoromethlated pyridones, and trifluoromethylated dihydropyridones are obtained. The reactions occur under mild conditions
Synthesis of Highly Substituted Pyridines through Copper-Catalyzed Condensation of Oximes and α,β-Unsaturated Imines
作者:Wei Wen Tan、Yew Jin Ong、Naohiko Yoshikai
DOI:10.1002/anie.201704378
日期:2017.7.3
A copper-catalyzed condensation reaction of oxime acetates and α,β-unsaturated ketimines to give pyridine derivatives is reported. The reaction features mild conditions, high functional-group compatibility, and high regioselectivity with respect to unsymmetrical oxime acetates, thus allowing the preparation of a wide range of polysubstituted pyridines, many of which are not readily accessible by conventional
copper-catalyzed coupling of oximeacetates with isothiocyanates. Various 4-substituted and 4,5-disubstituted 2-aminothiazoles were formed smoothly under mild reaction conditions. This process involved copper-catalyzed N–O bond cleavage, activation of vinyl sp2 C–H bonds, and C–S/C–N bond formations. It is noteworthy that the oximeacetates were used not only as a substrate but also as a single oxidant