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Light-Driven Intramolecular Cyclopropanation of Alkene-Tethered N -Tosylhydrazones: Synthesis of Fused-Cyclopropane γ-Lactones.

Pokhriyal YaminiAkanksha BabbarDongari Yadagiri
Published in: Organic letters (2024)
Fused-cyclopropane ring-containing γ-lactone compounds are versatile building blocks in many fields, including the synthesis of biologically active compounds. Here, we report the light-driven intramolecular cyclopropanation of alkene-tethered N -tosylhydrazones in the presence of Cs 2 CO 3 and visible light. We have synthesized various electronically and sterically substituted and heterocyclic-containing fused-(spiro)cyclopropane γ-lactone compounds in good yields under transition metal-free conditions using a radical-free approach. In addition, the one-pot synthesis of fused-cyclopropane γ-lactones from α-ketoesters and their synthetic utility are also presented.
Keyphrases
  • visible light
  • molecular docking
  • energy transfer
  • molecular dynamics simulations