4.7 Article

NbCl3-Catalyzed Intermolecular [2+2+2] Cycloaddition of Alkynes and α,ω-Dienes: Highly Chemo- and Regioselective Formation of 5-(ω-Alkenyl-1,4-substituted-1,3-cyclohexadiene Derivatives

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 75, Issue 17, Pages 6046-6049

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo101229u

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Funding

  1. MEXT, Japan
  2. Japan Science and Technology Agency (JST)
  3. Kansai University
  4. MEXT

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Intermolecular [2+2+2] cycloaddition of tert-butylacetylene with alpha,omega-dienes was successfully achieved by NbCl3(DME) catalyst to afford 5-omega-alkenyl-1,4-disubstituted-1,3-cyclohexadienes in excellent yields with high chemo- and regioselectivity.

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