Silyl-substituted diazoacetic esters in superacid media—a stable ion and solvolysis study
作者:Kenneth K. Laali、Gerhard Maas、Monika Gimmy
DOI:10.1039/p29930001387
日期:——
FSO3H or CF3SO3H, protonation, dediazoniation and gegenion addition occur without concomitant desilylation, whereas with HF, partial desilylation takes place. Upon solvolysis of 2, only desilylated esters are obtained. When 1 is allowed to react with the superacid FSO3H·SbF5(1 : 1)/SO2 at ⩽–75 °C, five major ions are formed, among them the silyl-substituted enoldiazonium ions (Z)- and (E)-9 corresponding
对于重氮(三异丙基甲硅烷基)乙酸甲酯(1)和重氮(五甲基二甲硅烷基)乙酸甲酯(2)而言,在超酸中的质子化和随后的化学反应,以及与非水酸(FSO 3 H,CF 3 SO 3 H的溶剂分解反应)(HF)已进行了研究。通过FSO 3 H或CF 3 SO 3 H溶剂化1时,质子化,脱重氮和gegeion加成发生而没有伴随的甲硅烷基化,而在HF的情况下,发生了部分甲硅烷基化。溶剂分解2时,仅获得去甲硅烷基化的酯。当1与超酸FSO 3反应时在⩽–75°C下,H·SbF 5(1:1)/ SO 2形成五个主要离子,其中甲硅烷基取代的烯重氮鎓离子(Z)-和(E)-9对应于O-质子化1和质子化的(氟磺酰氧基)乙酸盐4-H +。在较低酸度超强酸FSO 3 H / SO 2的ö -protonated silyldiazoesters [(Ž)-9,(ë)-9]和Ç,Ô -diprotonated(14 -H +
Laali Kenneth K., Maas Gerhard, Gimmy Monika, J. Chem. Soc. Perkin Trans, (1993) N 7, S 1387-1394
作者:Laali Kenneth K., Maas Gerhard, Gimmy Monika
DOI:——
日期:——
ALLSPACH, T.;GUEMBEL, H.;REGITZ, M., J. ORGANOMET. CHEM., 1985, 290, N 1, 3-39