DMF as an amine source: iron-catalyzed cyclization of 2H-azirines to imidazoles†
Abstract
A novel method has been developed for the synthesis of 1-methyl-4,5-diaryl-1H-imidazoles through Fe(II)-catalyzed cyclization of 2H-azirines and N,N-dimethylformamide (DMF) as an amine source. This transformation involves the cleavage of C–N and C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) N double bonds and the construction of new C–N and C
N double bonds and the construction of new C–N and C![[double bond, length as m-dash]](https://www.rsc.org/images/entities/char_e001.gif) N double bonds. The reaction has readily available starting materials, a wide range of substrates and mild reaction conditions. In addition, the reaction also facilitated the convenient synthesis of 1-methyl-2,4,5-triaryl-1H-imidazoles.
N double bonds. The reaction has readily available starting materials, a wide range of substrates and mild reaction conditions. In addition, the reaction also facilitated the convenient synthesis of 1-methyl-2,4,5-triaryl-1H-imidazoles.
 
                




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