332174-61-5Relevant academic research and scientific papers
Solvent-free synthesis of 1-amidoalkyl-2-naphthols using magnetic nanoparticle-supported?2-(((4-(1-iminoethyl)phenyl)imino)methyl)phenol Cu (II) or Zn (II) Schiff base complexes
Ghorbani, Fatemeh,Kiyani, Hamzeh,Pourmousavi, Seied Ali,Ajloo, Davood
, p. 3145 - 3164 (2020)
Two magnetic nanoparticle-supported?2-(((4-(1-iminoethyl)phenyl)imino)methyl)phenols were successfully synthesized, characterized, and applied in the one-pot three-component reaction of substituted benzaldehydes, 2-naphthol, and amides for synthesis of 1-
Sulfonated polynaphthalene as an effective and reusable catalyst for the one-pot preparation of amidoalkyl naphthols: DFT and spectroscopic studies
Pourmousavi, Seied Ali,Moghimi, Parvin,Ghorbani, Fatemeh,Zamani, Mehdi
, p. 87 - 102 (2017/05/15)
Sulfonated polynaphthalene (S-PNP) as a carbon-based solid acid efficiently catalyzed the one-pot three-component synthesis of amidoalkyl naphthols. The three-component process of substituted aryl aldehydes, 2-naphthol, and amide (benzamide and acetamide)
Efficient one-pot syntheses of betti bases catalyzed by 1-methyl-3-(2-(sulfooxy)ethyl)-1H-imidazol-3-ium chloride
Wang,Wan,Wang,Zhao,Shi,Zhang,Wu
, p. 496 - 500 (2013/06/27)
The efficient one-pot syntheses of Betti bases by the three-component reaction of aromatic aldehyde, 2-naphthalen, and acetonitrile (or benzamide) catalyzed by 1-methyl-3-(2-(sulfooxy)ethyl)-1H-imidazol-3-ium chloride is reported. The solvent can be recyc
Carboxyl-functionalized ionic liquids based on Benzimidazolium cation: Study of Hammett values and catalytic activity towards one-pot synthesis of 1-amidoalkyl naphthols
Muskawar, Prashant Narayan,Senthil Kumar,Bhagat, Pundlik Rambhau
, p. 112 - 117 (2013/11/19)
A series of new carboxyl-functionalized benzimidazolium based ionic liquids (CFBILs) were synthesized and characterized by FT-IR, NMR and HR-MS (EI). Catalytic activities of CFBILs were evaluated towards the solvent free, one-pot synthesis of 1-amidoalkyl
1,3-Dibromo 5,5-dimethylhydantoin (DBH) catalyzed, microwave-assisted rapid synthesis of 1-amidoalkyl-2-naphthols
Habibzadeh, Setareh,Ghasemnejad-Bosra, Hassan
experimental part, p. 193 - 198 (2012/07/03)
An expeditious synthesis of 1-amidoalkyl-2-naphthols by the condensation of 2-naphthole with various araldehydes and acetamide is described. This greener protocol is catalyzed by 1,3-dibromo 5,5-dimethylhydantoin (DBH), and proceeds efficiently in the abs
Atom-efficient and environment-friendly multicomponent synthesis of amidoalkyl naphthols catalyzed by P2O5
Nandi, Ganesh Chandra,Samai, Subhasis,Kumar, Ram,Singh
experimental part, p. 7220 - 7222 (2010/03/03)
An atom-efficient and environment-friendly approach for the synthesis of amidoalkyl naphthols (4a-x) via multicomponent one-pot reaction of 2-naphthol (1), aromatic aldehyde (2) and amide (3) catalyzed by P2O5 has been developed. The
P2O5-hexamethyldisiloxane (HMDS): An efficient system to induce the three-component reaction of enolic systems, aromatic aldehydes, and acetonitrile
Anary-Abbasinejad, Mohammad,Anaraki-Ardakani, Hossein,Hassanabadi, Alireza
, p. 3706 - 3716 (2008/12/23)
Three-component reaction of an enolizable compound, such as acetophenone, methyl acetoacetate, 4-hydroxycoumarin, 2-naphthol, or 3-hydroxy-2-naphthoic acid; an aromatic aldehyde, and acetonitrile induced by phosphorus pentoxide and hexamethyldisiloxane le
Three-component reaction between 2-naphthol, aromatic aldehydes and acetonitrile in the presence of chlorosulfonic acid yields 1-(acetylamino (aryl)methyl)-2-naphthols
Anary-Abbasinejad, Mohammad,Hassanabadi, Alireza,Kamali-Gharamaleki, Maryam,Saidipoor, Azimeh,Anaraki-Ardakani, Hossein
, p. 644 - 646 (2008/09/18)
The one-pot, three-component reaction between aryl aldehydes, 2-naphthol, and acetonitrile in the presence of chlorosulfonic acid affords 1-[acetylamino(aryl)methyl]-2-naphthols in excellent yields.
