RT Journal Article
T1 Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones
A1 Luna Costales, Amparo
A1 Herrera García, Fernando
A1 Almendros Requena, Pedro
A1 Fernández López, Israel
AB 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.
PB Royal Society of Chemistry
SN 1359-7345
YR 2019
FD 2019-12-19
LK https://hdl.handle.net/20.500.14352/113815
UL https://hdl.handle.net/20.500.14352/113815
LA eng
NO Herrera Fernando, Luna Amparo, Fernández Israel,  Almendros Pedro. Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones. Chem. Commun., 2020, 56 (8), 1290-1293
NO Ministerio de Ciencia e Innovación (España)
NO European Commission
DS Docta Complutense
RD 10 abr 2025