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.
2025
carbocycles; cascade reactions; heterocycles; small ring systems; synthetic methods
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/447646
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