TY  - JOUR
AU  - Martín-Mejías, Irene
AU  - Aragoncillo Abanades, Cristina
AU  - Yanai, Hikaru
AU  - Hoshikawa, Shoki
AU  - Fujimoto, Yuuki
AU  - Matsumoto, Takashi
AU  - Almendros Requena, Pedro
PY  - 2020
DO  - 10.1039/c9cc08930f
SN  - 1359-7345
UR  - https://hdl.handle.net/20.500.14352/91838
T2  - Chemical Communications
AB  - Carbazoles possessing Tf2CHCH2 groups were obtained by the reaction of 1-(indol-2-yl)but-3-yn-1-ols with in situ-generated Tf2CQCH2 through vicinal difunctionalisation of the alkyne moiety, where the vinyl-type carbocation intermediate was selectively...
LA  - eng
M2  - 1795
PB  - The Royal Society of Chemistry
KW  - Carbazole
KW  - Zwitterion
KW  - Alkynol
KW  - Triflyl group
TI  - A catalyst-free bis(triflyl)ethylation/benzannulation reaction: rapid access to carbazole-based superacidic carbon acids from alkynols
TY  - journal article
VL  - 56
ER  -