C(sp 3 )–H cyclizations of 2-(2-vinyl)phenoxy- tert -anilines

Dunkel, Petra ✉ [Dunkel, Petra (Szerves-és gyógys...), author] Department of Organic Chemistry (SU / FP); Bogdán, Dóra [Bogdán, Dóra (Szerves kémia, gy...), author] Department of Organic Chemistry (SU / FP); Deme, Ruth [Deme, Ruth (Szerves-és gyógys...), author] Department of Organic Chemistry (SU / FP); Zimber, Ádám; Ballayová, Veronika; Csizmadia, Eszter; Kontra, Bence [Kontra, Bence (Szerves Kémia), author] Department of Organic Chemistry (SU / FP); BrainVisionCenter Research Institute and Compet...; Kalydi, Eszter [Kalydi, Eszter (NMR spektroszkópia), author] Department of Organic Chemistry (SU / FP); Bényei, Attila [Bényei, Attila Csaba (Polimorfia kutatá...), author] Fizikai Kémiai Tanszék (UD / IChem); Mátyus, Péter [Mátyus, Péter (Szerves- és gyógy...), author] Department of Organic Chemistry (SU / FP); University of Veterinary Medicine Budapest; Mucsi, Zoltán ✉ [Mucsi, Zoltán (szerves kémia), author] Kémiai Intézet (UM / AVK); Femtonics Ltd.; BrainVisionCenter Research Institute and Compet...

English Article (Journal Article) Scientific
Published: RSC ADVANCES 2046-2069 2046-2069 14 (24) pp. 16784-16800 2024
  • SJR Scopus - Chemical Engineering (miscellaneous): Q1
Identifiers
Fundings:
  • (BO/799/21/7) Funder: MTA Bolyai pályázat
  • (ÚNKP-23-ME4)
  • (TKP2021-NVA-14)
  • (2020-2.1.1-ED-2022-00208)
  • (SNN 135825) Funder: NKFIH
Subjects:
  • Chemical sciences
Cyclizations of 2-(2-vinyl)phenoxy- tert -anilines under thermal conditions yield oxazonine or octahydro-dipyrroloquinoline products. The transformations can be considered as further extensions of [1, n ]-H transfer and cyclization of tertiary anilines.
Citing (11)
Citation styles: IEEEACMAPAChicagoHarvardCSLCopyPrint
2025-04-01 23:14