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Rhodium(III)-Catalyzed Synthesis of Isoquinolines from Aryl Ketone <i>O</i>-Acyloxime Derivatives and Internal Alkynes

Organic Letters · 2010 · Vol. 12(24) · pp. 5688–5691
Pei Chui TooYi‐Feng WangShunsuke Chiba

Abstract

A synthetic method of isoquinolines from aryl ketone O-acyloxime derivatives and internal alkynes has been developed using [Cp*RhCl(2)](2)-NaOAc as the potential catalyst system. The present transformation is carried out by a redox-neutral sequence of C-H vinylation via ortho-rhodation and C-N bond formation of the putative vinyl rhodium intermediate on the oxime nitrogen, where the N-O bond of oxime derivatives could work as an internal oxidant to maintain the catalytic cycle.

Catalytic C–H Functionalization MethodsSynthesis and Catalytic ReactionsAsymmetric Hydrogenation and CatalysisChemistryRhodiumOximeCatalysisKetoneArylCatalytic cycleMedicinal chemistryOrganic chemistryCombinatorial chemistry
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