4.8 Article

CuI-Catalyzed C1-Alkynylation of Tetrahydroisoquinolines (THIQs) by A3 Reaction with Tunable Iminium Ions

Journal

ORGANIC LETTERS
Volume 15, Issue 23, Pages 5928-5931

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol402517e

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Funding

  1. Natural Science Foundation of China [21232001]
  2. National Basic Research Program of China-973 Program [2010CB833203]

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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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