882866-41-3Relevant articles and documents
Mild, rapid and efficient metal-free synthesis of 2-aryl-4-aryloxyquinolines via direct Csp2[sbnd]O bond formation by using diaryliodonium salts
Nahide, Pradip D.,Solorio-Alvarado, César R.
, p. 279 - 284 (2017)
An efficient ligand- and transition metal-free procedure for the direct Csp2[sbnd]O bond formation for the arylation of 2-aryl-4-quinolones was developed. The synthesis of the starting quinolones was carried out under our optimized C
Photoredox halogenation of quinolones: The dual role of halo-fluorescein dyes
Ritu,Kumar, Sharvan,Chauhan, Parul,Jain, Nidhi
, p. 4585 - 4592 (2021/05/31)
An efficient C-3 halogenation of quinolin-4-ones is reported with halogenated fluorescein dyes which serve both as a halogen source and photocatalyst. This reaction shows broad substrate scope and gives good to excellent yields of C-3 brominated/iodinated
Synthesis and cyclisation studies of (E)-2-aryl-1-methyl-3-styrylquinolin-4(1H)-ones
Rocha, Djenisa H.A.,Pinto, Diana C.G.A.,Silva, Artur M.S.
supporting information, p. 7717 - 7721 (2015/09/07)
The synthesis of (E)-2-aryl-1-methyl-3-styrylquinolin-4(1H)-ones, through the Heck reaction of 2-aryl-3-iodo-1-methyl-quinolin-4(1H)-ones with styrene is described. 2-Aryl-3-iodo-1-methyl-2-quinolin-4(1H)-ones can be obtained efficiently in a two-step tra
