4.8 Article

Exploring the Reactivity of N-Alkynylated Sulfoximines: [2+2]-Cycloadditions

Journal

ORGANIC LETTERS
Volume 15, Issue 21, Pages 5397-5399

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol4026028

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Funding

  1. Alexander von Humboldt Foundation
  2. Cluster of Excellence (Tailor-Made Fuels from Biomass)
  3. Excellence Initiative of the German federal and state governments

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To assess the potential of N-alkynylated sulfoximines as new (chiral) reagents for organic synthesis, their reactivity profile in numerous synthetic processes is under investigation. When reacted with ketenes, the alkynylated-sulfoximines undergo a [2 + 2]-cycloaddition process to afford sulfoximine-functionalized cyclobutenones in excellent yields.

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