Abstract
Trimethylsilylation of 1,2,3-triazole regioselectively proceeded to give 2-trimethylsilyl-2H-1,2,3-triazole, which was treated with primary alkyl halides in the presence of tetrabutylammonium fluoride to give 1-alkyl-1H- 1,2,3-triazoles as a Sole product 1-Methyl-5-substituted 1H-1,2,3-triazoles were prepared by alkylation of 5-lithio-1-methyl-1H-1,2,3-triazole, and 1- methyl-4-substituted 1H-1,2,3-triazoles were obtained by alkylation of 4- lithio-1-methyl-5-phenylthio-1H-1,2,3-triazole followed by reductive desulfurization.
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CITATION STYLE
Ohta, S., Kawasaki, I., Uemura, T., Yamashita, M., Yoshioka, T., & Yamaguchi, S. (1997). Alkylation and acylation of the 1,2,3,triazole ring. Chemical and Pharmaceutical Bulletin, 45(7), 1140–1145. https://doi.org/10.1248/cpb.45.1140
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