A cascade reaction has been established that enables access to structurally diverse 2-oxabicyclo[3.2.0]heptan-3-ones bearing a benzo[d]oxazol-2(3H)-one moiety at the bridgehead quaternary center in moderate to good yields in a single operation. The reaction illustrates the potential of 2-hydroxycyclobutanone as a substrate for the rapid preparation of unusual and complex molecular frameworks.
Synthesis of β‐N‐Heterocyclic‐Cyclobutane‐Fused Bicyclic γ‐Lactones from 2‐Hydroxycyclobutanone and Carboxamide‐Bearing Wittig Reagents
Barranco, Stefano;Uras, Mauro;Frau, Veronica;Caboni, Pierluigi;Frongia, Angelo
2025-01-01
Abstract
A cascade reaction has been established that enables access to structurally diverse 2-oxabicyclo[3.2.0]heptan-3-ones bearing a benzo[d]oxazol-2(3H)-one moiety at the bridgehead quaternary center in moderate to good yields in a single operation. The reaction illustrates the potential of 2-hydroxycyclobutanone as a substrate for the rapid preparation of unusual and complex molecular frameworks.File in questo prodotto:
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Eur J Org Chem - 2025 - Barranco - Synthesis of ‐N‐Heterocyclic‐Cyclobutane‐Fused Bicyclic ‐Lactones from.pdf
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