RT info:eu-repo/semantics/article
T1 Mild-base-promoted arylation of (hetero)arenes with anilines
A1 Martín García, Víctor Sotero
A1 Santos, Tanausú
A1 Monzón, Diego M.
A1 Pinacho-Crisóstomo, F.
A1 Carrillo, Romen
K1 C−C coupling
K1 diazo compounds
K1 dyes/pigments
K1 heterocycles
K1 radical reactions
K1 heterociclos
K1 reacciones radicales
AB Transition metal-free radical arylation of heteroarenes is achieved at room temperature by simply adding aqueous sodium carbonate to a solution of the corresponding heteroarene and arenediazonium salt, which can even be formed in situ. Such an easy, inexpensive and mild methodology has been optimized and applied to the expeditious modification of interesting molecular cores like naphthylimide or bisthienylcyclopentenes.
YR 2018
FD 2018
LK http://riull.ull.es/xmlui/handle/915/16139
UL http://riull.ull.es/xmlui/handle/915/16139
LA en
DS Repositorio institucional de la Universidad de La Laguna
RD 19-abr-2024