118988-25-3Relevant articles and documents
I2/TBHP promoted isocyanide insertion cyclization reaction for the synthesis of quinazolin fused benzoimidazole as a selective methanol detection probe
Ahmadi, Fereshteh,Ahmadi, Nafiseh,Balmohammadi, Yaser,Bazgir, Ayoob,Naimi-Jamal, Mohammad Reza
, (2021/06/16)
An efficient I2/TBHP promoted isocyanide insertion cyclization reaction for the synthesis of quinazolines-fused benzoimidazole was reported. The synthesized compounds have a unique potential to use as a selective solvatochromic fluorescence pro
HETEROCYCLIC SYNTHESIS VIA A TANDEM AZA-WITTIG REACTION/ HETEROCUMULENE-MEDIATED ANNULATION REACTION.NEW METHODOLOGY FOR THE PREPARATION OF QUINAZOLINE DERIVATIVES.
Molina, Pedro,Alajarin, Mateo,Vidal, Angel
, p. 3849 - 3852 (2007/10/02)
The aza-Wittig reaction of iminophosphoranes derived from N-substituted o-azidobenzamides or 2-(o-azido)phenyl benzimidazole with isocyanates, carbon dioxide or carbon disulphide, lead to functionalized 4(3H)-quinazolinones and benzimidazoquinazolines respectively.