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. 2018 Jul 11;8(44):24913–24922. doi: 10.1039/c8ra04389b

Scheme 1. Synthesis of triazoles 4–9 and 12–15. Reagents and conditions: (a) NaOMe, MeOH, rt; (b) alkyne, CuI, DIPEA, MeCN, 50 °C; (c) (i). 1-{[2-(Trimethylsilyl)ethoxy]methyl}-4-[2-(trimethylsilyl)ethynyl]-1H-imidazole, CuI, DIPEA, MeCN, 50 °C; (ii). BF3OEt2, CH2Cl2, rt; (d) methyl thioglycolate, BF3 OEt2, CH2Cl2, rt; (e) (i). Alkyne, CuI, DIPEA, MeCN, 50 °C; (ii). NaOMe, MeOH, rt; (iii). LiOH, THF : H2O (9 : 1), rt. Tol = p-methylphenyl.

Scheme 1