Functionalization of 1-methyl-1H-imidazole-5-carboxylic acid at the C-2 position: efficient syntheses of 2-substituted t-butyl 1-methyl-1H-imidazole-5-carboxylates
Jp. Collman et al., Functionalization of 1-methyl-1H-imidazole-5-carboxylic acid at the C-2 position: efficient syntheses of 2-substituted t-butyl 1-methyl-1H-imidazole-5-carboxylates, J CHEM R-S, (5), 2000, pp. 230-231
A number of 2-substituted t-butyl 1-methyl-1H-imidazole-5-carboxylates, whi
ch can be readily converted to the corresponding acids, were efficiently pr
epared from t-butyl 2-bromo-1-methyl-1H-imidazole-5-carboxylate via bromine
lithium exchange or palladium-catalysed coupling.