Fernández de Trocóniz Guillermo, Ochoa de Retana Ana M, Rubiales Gloria, Palacios Francisco
Departamento de Química Orgánica I and Centro de Investigacion Lascaray (Lascaray Research Center) Facultad de Farmacia, Universidad del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU) , Paseo de la Universidad 7, 01006 Vitoria, Spain.
J Org Chem. 2014 Jun 6;79(11):5173-81. doi: 10.1021/jo500745u. Epub 2014 May 13.
A regioselective addition of isocyanates to fluoroalkylated α,β-unsaturated imines 1 is described. Fluoroalkyl-substituted triazinane-2,4-diones 4 are obtained by the reaction of phenyl isocyanate with fluorinated imines 1, while fluorinated dihydropyridin-2(1H)-ones 7 are prepared when tosyl isocyanate is used. Tetrahydro-pyridin-2(1H)-one 10 is obtained by catalytic reduction of dihydropyridin-2(1H)-one 7. Computational studies are performed to explain the different behaviors of both isocyanates and the mechanisms of the processes.
本文描述了异氰酸酯对氟烷基化α,β-不饱和亚胺1的区域选择性加成反应。苯基异氰酸酯与氟化亚胺1反应可得到氟烷基取代的三嗪烷-2,4-二酮4,而使用甲苯磺酰异氰酸酯时则可制备氟化二氢吡啶-2(1H)-酮7。二氢吡啶-2(1H)-酮7经催化还原可得到四氢吡啶-2(1H)-酮10。进行了计算研究以解释两种异氰酸酯的不同行为及反应过程的机理。