RT Journal Article
T1 Synthesis of polycyclic aromatic hydrocarbons decorated by fluorinated carbon acids/carbanions
A1 Hoshikawa, Shoki
A1 Yanai, Hikaru
A1 Martín‐Mejías, Irene
A1 Lázaro Milla, Carlos
A1 Aragoncillo Abanades, Cristina
A1 Almendros Requena, Pedro
A1 Matsumoto, Takashi
AB The carboarylation reaction of biphenyl‐alkynes was successfully triggered by electrophilic attack of 1,1‐bis(triflyl)ethylene on the alkyne moiety to give polycyclic aromatic hydrocarbons (PAHs) decorated by superacidic carbon acid functionality. Neutralisation of thus obtained acids with NaHCO3 yielded the corresponding sodium salts, which showed improved solubility in both aqueous and organic solvents.
PB Wiley-VCH GmbH
SN 0947-6539
YR 2021
FD 2021
LK https://hdl.handle.net/20.500.14352/91828
UL https://hdl.handle.net/20.500.14352/91828
LA eng
NO Hoshikawa S, Yanai H, Martín-Mejías I, Lázaro-Milla C, Aragoncillo C, Almendros P, Matsumoto T. Synthesis of Polycyclic Aromatic Hydrocarbons Decorated by Fluorinated Carbon Acids/Carbanions, 2021, 27, 16112-16116.
NO Ministerio de Ciencia e Innovación (España)
NO European Commission
DS Docta Complutense
RD 31 ago 2024