Synthesis , 2010,06, 979-984
DOI: 10.1055/s-0029-1218633
Khodakovskiy P. V.; Mykhailiuk P. K.; Volochnyuk D. M.; Tolmachev A. A.
A set of electrophilic 2-(trifluoroacetyl)-1,3-azoles demonstrated excellent activity in the C-oxyalkylation of pyrrole, furan, thiophene, 1,3-thiazole, and 1,2-oxazole derivatives. The reaction conditions and the yields of the corresponding trifluoromethyl-substituted alcohols depend strongly on both the electronic and steric nature of the 1,3-azole unit.
Khodakovskiy P. V.; Mykhailiuk P. K.; Volochnyuk D. M.; Tolmachev A. A.
Synthesis 2010, 06, 979-984
DOI: 10.1055/s-0029-1218633