4.8 Article

Synthesis of Spirocyclic γ-Lactones by Cascade Beckwith-Dowd Ring Expansion/Cyclization

Journal

ORGANIC LETTERS
Volume 14, Issue 13, Pages 3412-3415

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol301386k

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Funding

  1. ARC
  2. Monash Research Accelerator Program

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A range of spirocyclic gamma-lactones have been prepared exploiting a Beckwith-Dowd ring expansion cascade involving 1-, 3-, 4-, and 5-carbon expansion of cyclopentanone and cyclohexanone followed by 5-exo-trig or 5-exo-dig cyclization. This radical cascade reaction can be achieved with various substrates to provide a broad range of gamma-lactones spirofused to 6- to 10-membered cycloalkanones.

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