RT info:eu-repo/semantics/article
T1 Straight access to highly fluorescent angular indolocarbazoles via merging Au- and Mo-catalysis
A1 Martínez Lara, Fernando
A1 Suárez, Anisley
A1 Suarez Pantiga, Samuel
A1 Tapia Estévez, M" José
A1 Sanz Díez, Roberto
K1 Química orgánica
K1 Chemistry, Organic
AB A straightforward and efficient synthesis of the two less explored types of indolocarbazoles has beendeveloped. Two different processes for the carbazole nucleus preparation, a gold-catalysed regioselectivecyclization followed by the dioxomolybdenum-catalysed version of Cadogan reductive cyclization,enables the sequential construction of two carbazole cores. The procedure features total regioselectivityand high overall yields. The required starting α-indol-3-ylalkyl propargylic alcohols are easily and efficientlyaccessed from commercially available reagents. In addition, the photoluminescent properties of twoindolo[2,3-c]carbazoles, with fluorescence quantum yields around 0.7, have been studied.
PB Royal Society of Chemistry
YR 2020
FD 2020-07
LK http://hdl.handle.net/10259/5401
UL http://hdl.handle.net/10259/5401
LA eng
NO Junta de Castilla y León and FEDER (BU291P18) and Ministerio de Ciencia e Innovación and FEDER (CTQ2016-75023-C2-1-P)
DS Repositorio Institucional de la Universidad de Burgos
RD 26-abr-2024