State Key Laboratory of Respiratory Disease, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, China.
Chemistry. 2012 Oct 29;18(44):13964-7. doi: 10.1002/chem.201202271. Epub 2012 Sep 20.
A metal-free synthesis of diversified benzimidazoles from N-arylamidines through a phenyliodine(III) diacetate (PIDA) promoted intramolecular direct C(sp(2))-H imidation has been developed. The reaction proceeds smoothly at 0 °C or ambient temperature to provide the desired products in good to excellent yields. The synthesis of 2-alkyl- or 2-alkyl-fused benzimidazoles, which are generally inaccessible by similar Pd- or Cu-catalyzed approaches, can also be achieved.
一种通过苯碘酰二乙酸(PIDA)促进的分子内直接 C(sp(2))-H 亚胺化反应,从 N-芳基酰胺合成多样化苯并咪唑的无金属合成方法已经被开发出来。该反应在 0°C 或室温下顺利进行,以良好至优异的收率提供所需产物。通过类似的 Pd 或 Cu 催化方法通常难以合成的 2-烷基-或 2-烷基稠合苯并咪唑也可以通过这种方法合成。