2007
DOI: 10.1002/chin.200802077
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ChemInform Abstract: Ferric Perchlorate‐Catalyzed One‐Pot Synthesis of α‐Aminonitriles Using Trimethylsilylcyanide.

Abstract: Nitriles Q 0520Ferric Perchlorate-Catalyzed One-Pot Synthesis of α-Aminonitriles Using Trimethylsilylcyanide. -(OSKOOIE, H. A.; HERAVI*, M. M.; SADNIA, A.; JANNATI, F.; BEHBAHANI, F. K.; Synth. Commun. 37 (2007) 15, 2543-2548; Dep. Chem., Sch. Sci., Azzahra Univ., Vanak, Tehran, Iran; Eng.) -R. Langenstrassen 02-077

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“…The 2-aryl-1-arylmethyl-1H-1,3-benzimidazoles were obtained in good yields by the reaction of o-phenylenediamine derivatives with various aldehydes in the presence of ferric perchlorate in the absence of solvent at ambient temperature. The method has the ability to tolerate other functional groups such as methyl, methoxy, nitro and chloro groups (Scheme 19) [120].…”
Section: Scheme 18mentioning
confidence: 99%
“…The 2-aryl-1-arylmethyl-1H-1,3-benzimidazoles were obtained in good yields by the reaction of o-phenylenediamine derivatives with various aldehydes in the presence of ferric perchlorate in the absence of solvent at ambient temperature. The method has the ability to tolerate other functional groups such as methyl, methoxy, nitro and chloro groups (Scheme 19) [120].…”
Section: Scheme 18mentioning
confidence: 99%