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CuI-Catalyzed C1-Alkynylation of Tetrahydroisoquinolines (THIQs) by A<sup>3</sup> Reaction with Tunable Iminium Ions
109
Citations
42
References
2013
Year
Redox Neutral C1-alkynylationCross-coupling ReactionEngineeringOrganic ChemistryCui-catalyzed AOrganometallic CatalysisCatalysisChemistryCui-catalyzed C1-alkynylationTunable Iminium IonsBiomolecular EngineeringC1-alkynylated Thiq Products
A CuI-catalyzed A(3) (amines, aldehydes and alkynes) reaction of tetrahydroisoquinolines (THIQs), aldehydes, and alkynes to give C1-alkynylated THIQ products (endo-yne-THIQs) was developed. This redox neutral C1-alkynylation of THIQs, which was conducted under mild conditions, has a broad scope for the used aldehydes and alkynes. It was proposed that the A(3) reaction first generates in situ exo-iminium ions, which then isomerize to endo-iminium ions and react with copper acetylides to give the endo alkynylated THIQs (endo-yne-THIQs).
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