144406-85-9Relevant academic research and scientific papers
Tandem pericyclic reactions. The first X-ray structure of an initial pyrone-olefin adduct and an easy, stereocontrolled, entry into polyoxygenated cyclohexanes
Marko,Seres,Swarbrick,Staton,Adams
, p. 5649 - 5652 (1992)
Under high-pressure conditions, 2-pyrone undergoes Diels-Alder reaction with a variety of dienophiles, leading to isolable, bridged, bicyclic lactones. The first X-Ray structure of one of these lactones and its conversion into polyoxygenated cyclohexane d
