313240-02-7Relevant academic research and scientific papers
A new laccase-catalyzed domino process and its application to the efficient synthesis of 2-aryl-1H-benzimidazoles
Leutbecher, Heiko,Constantin, Mihaela-Anca,Mika, Sabine,Conrad, Jürgen,Beifuss, Uwe
, p. 605 - 608 (2011)
The laccase-catalyzed domino reaction of o-phenylenediamine and benzaldehydes with aerial oxygen as the oxidant exclusively yields 2-aryl-1H-benzimidazoles in good to very good yields. It is easy to perform under very mild reaction conditions.
Opianic acid in the synthesis of benzimidazole derivatives
Borodkin,Ukhin, L. Yu.,Belousova,Shepelenko,Alekseenko
, p. 118 - 120 (2017)
Heating an equimolar mixture of opianic acid and o-phenylenediamine in MeOH or EtOH produced 2-(2-carboxy-3,4-dimethoxyphenyl)benzimidazole, which was readily dehydrated in refluxing acetic or propionic anhydride to 11H-1,2-dimethoxyisoindolo[2,3-a]benzim
