ALKYLATION OF IMIDAZOLE AND BENZIMIDAZOLE DERIVATIVES WITH 1-(IODOMETHYL)-1,1,3,3,3-PENTAMETHYLDISILOXANE – A NEW METHOD FOR THE PREPARATION OF ORGANOCYCLOSILOXANE IODIDES
DOI:
https://doi.org/10.1007/2302Keywords:
2-aminobenzimidazole, benzimidazole, imidazole, 1-(iodomethyl)-1, 1, 3, 3-pentamethyldisiloxane, 2-methylimidazole, organocyclosiloxanes, alkylationAbstract
The reaction of imidazole and benzimidazole derivatives with 1-(iodomethyl)-1,1,3,3,3-pentamethyldisiloxane resulted in N1,3-alkylation, cleavage of siloxane bonds by the evolved hydrogen iodide, and the formation of cyclic organosilicon iodides and triiodides.
How to Cite
Zhilitskaya, L. V.; Yarosh, N. O.; Shagun, L. G.; Dorofeev, I. A.; Larina, L. I. Chem. Heterocycl. Compd. 2015, 51, 381. [Khim. Geterotsikl. Soedin. 2015, 51, 381.]
For this article in the English edition see DOI 10.1007/s10593-015-1711-8