%0 Journal Article
%A Luna Costales, Amparo
%A Herrera García, Fernando
%A Almendros Requena, Pedro
%A Fernández López, Israel
%T Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones
%D 2019
%@ 1359-7345
%U https://hdl.handle.net/20.500.14352/113815
%X The controlled synthesis of 1,4-naphthoquinones and tetraphene7,12-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]naphthalen4(2H)-ones.
%~