863311-15-3Relevant academic research and scientific papers
Competition of the R3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: A novel binucleophilic system for three-component synthesis of 2-aminofurans
Alizadeh, Abdolali,Rostamnia, Sadegh,Zhu, Long-Guan
, p. 1788 - 1792 (2008)
We recently reported a new class of triphenylphosphine and isocyanide based multicomponent reactions (Ph3P/DAAD and IMCRs/DAAD) mediated by R3P/DAAD and RNC/DAAD zwitterionic intermediates in the presence of CH, OH, and NH acids. Her
A modified and green methodology for preparation of polysubstituted furans
Azizian, Javad,Mohammadizadeh, Mohammad R.,Mohammadi, Ali A.,Karimi, Ali R.
, p. 259 - 262 (2005)
In this study, we introduced a very simple, one-pot and green methodology for preparation of polysubstituted furans by reaction of aromatic aldehydes, DMAD, and alkylisocyanides in water and at room temperature.
A novel synthesis of aminofurans using a four-component reaction
Alizadeh, Abdolali,Rostamnia, Sadegh,Zoreh, Nasrin,Oskueyan, Qasem
, p. 1610 - 1612 (2007)
Protonation of the reactive intermediate produced in the reaction between triphenylphosphine and dialkyl acetylenedicarboxylates by carboxylic acid leads to vinylphosphonium salts, which undergo nucleophilic reaction with carboxylate anion to produce dial
Reaction between isocyanides, dialkyl acetylenedicarboxylates and 2-hydroxy-1-aryl-2-(arylamino)ethanones: One-pot synthesis of highly functionalized 2-aminofurans
Mosslemin, Mohammad Hossein,Anary-Abbasinejad, Mohammad,Anaraki-Ardakani, Hossein
experimental part, p. 2676 - 2678 (2010/03/03)
A facile synthesis of highly functionalized 2-aminofuran derivatives by the multicomponent reaction of alkyl isocyanides, dialkyl acetylenedicarboxylates and 2-hydroxy-1-aryl-2-(arylamino)ethanone is described. The reaction is characterized by mild condit
Reaction of benzoyl chlorides with Huisgen's zwitterion: synthesis of functionalized 2,5-dihydro-1H-pyrroles and tetrasubstituted furans
Yavari, Issa,Mokhtarporyani-Sanandaj, Ako,Moradi, Loghman,Mirzaei, Anvar
, p. 5221 - 5225 (2008/09/21)
The 1:1 intermediate generated by the addition of alkyl(aryl) isocyanides to dimethyl acetylenedicarboxylate is trapped by benzoyl chloride to yield functionalized 2,5-dihydro-1H-pyrroles. The presence of electron-withdrawing groups at the para position o
