THE FIRST EXAMPLE OF AN UNUSUAL REARRANGEMENT IN THE VAN LEUSEN IMIDAZOLE SYNTHESIS
DOI:
https://doi.org/10.1007/2663Ключевые слова:
TosMIC, imidazole, ketimine, enamine, bismuth(III) triflateАннотация
The synthesis of an 1,4-disubstituted 5-methylimidazole is reported by reacting toluenesulfonylmethyl isocyanide with an enaminic tautomeric form of a secondary ketimine in the presence of catalytic amounts of bismuth(III) triflate. A possible mechanism involving a tosyl substitution on the imidazoline intermediate is proposed. This work represents a novel application for the versatile reagent toluenesulfonylmethyl isocyanide that expands its use to the preparation of imidazole starting from ketimine compounds.
How to Cite
Fodili, M.; Nedjar-Kolli, B.; Vedrenne, M.; Saffon-Merceron, N.; Lherbet, C.; Hoffmann, P. Chem. Heterocycl. Compd. 2015, 51, 940. [Khim. Geterotsikl. Soedin. 2015, 51, 940.]
For this article in the English edition see DOI 10.1007/s10593-015-1801-7
