作者:W.J. Middleton、E.M. Bingham
DOI:10.1016/s0022-1139(00)81231-2
日期:1983.6
Several novel α-trifluoromethylarylacetic acids were synthesized, utilizing chloropentafluoroacetone as the source of the trifluoromethyl group. One of these new acids, the trifluoro- analog (30) of ibuprofen, showed antiinflammatory, analgesic, and ulcerogenic properties similar to ibuprofen.
利用氯五氟丙酮作为三氟甲基的来源,合成了几种新型的α-三氟甲基芳基乙酸。这些新酸中的一种,布洛芬的三氟类似物(30)具有与布洛芬相似的抗炎,镇痛和促溃疡作用。