753000-30-5Relevant academic research and scientific papers
Facile synthesis of oxabicyclic alkenes by ultrasonication-promoted Diels-Alder cycloaddition of furano Dienes
Wei, Kun,Gao, Hai-Tao,Li, Wei-Dong Z.
, p. 5763 - 5765 (2007/10/03)
Ultrasonic irradiation effectively promotes the Diels-Alder reaction of substituted furans with reactive dienophiles (i.e., dimethyl acetylenedicarboxylate (DMAD) and dimethyl maleate). Regiospecific furano Diels-Alder cycloaddition of 2-vinylic furans with DMAD furnished functionalized oxabicyclic alkenes in good yield under ultrasonication condition.
