72853-74-8Relevant academic research and scientific papers
Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: Controlled access to functionalized quinones
Herrera, Fernando,Luna, Amparo,Fernández, Israel,Almendros, Pedro
supporting information, p. 1290 - 1293 (2020/02/04)
The controlled synthesis of 1,4-naphthoquinones and tetraphene-7,12-diones, which bear the ABCD-ring of landomycins, has been accomplished directly through oxidative rearrangement of common stable precursors, namely, previously non-isolable cyclobuta[a]naphthalen-4(2H)-ones.
Facile Photochemical Synthesis of Polycyclic Aromatic Compounds
Maruyama, Kazuhiro,Otsuki, Tetsuo,Mitsui, Kiichiro
, p. 1424 - 1428 (2007/10/02)
A variety of polycyclic aromatic quinones, which easily reduced to the corresponding aromatic hydrocarbons, were synthesized via one-pot photocycloaddition reaction of simple 2-halogenated 1,4-naphthoquinone derivatives with 1,1-disubstituted ethylenes.Th
