TY  - JOUR
AU  - Luna Costales, Amparo
AU  - Herrera García, Fernando
AU  - Almendros Requena, Pedro
AU  - Fernández López, Israel
PY  - 2019
DO  - 10.1039/C9CC08628E
SN  - 1359-7345
UR  - https://hdl.handle.net/20.500.14352/113815
T2  - Chemical Communications
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...
LA  - eng
M2  - 1290
PB  - Royal Society of Chemistry
KW  - quinone
KW  - 1,4-naphthoquinones
KW  - allenynols
TI  - Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones
TY  - journal article
VL  - 56
ER  -