Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52056 Aachen, Germany.
Org Lett. 2011 Feb 18;13(4):768-71. doi: 10.1021/ol103030w. Epub 2011 Jan 14.
N-Protected trifluoromethyl-substituted sulfoximines have been prepared by treatment of sulfonimidoyl fluorides with a combination of the Ruppert-Prakash reagent (TMSCF(3)) and tetrabutyl ammonium fluoride (TBAF). The starting materials were accessed following two synthetic routes, and for each reaction sequence the substrate scope was evaluated. Accordingly, a wide variety of aryl-substituted products were obtained in moderate to good yield.
N-保护的三氟甲基取代的亚磺酰胺已通过磺酰亚胺氟化物与 Ruppert-Prakash 试剂(TMSCF(3))和四丁基氟化铵(TBAF)的组合处理来制备。起始材料是通过两种合成路线获得的,并且对于每个反应序列都评估了底物范围。因此,以中等至良好的收率获得了各种芳基取代的产物。