Zur anodischen Dehydrodimerisierung von Triacylmethanen: Synthese und Reaktionen substituierter 4,7,8-Trioxabicyclo[3.2.1]octene-(2)
作者:Hans Günter Thomas、Ulrich Wellen、Josef Simons、Gerhard Raabe
DOI:10.1055/s-1993-26012
日期:——
On the Anodic Dehydrodimerization of Triacylmethanes: Synthesis and Reactions of Substituted 4,7,8-Trioxabicyclo[3.2.1]octenes ß-Tricarbonylic compounds 1 can be oxidized anodically in acetonitrile containing some triethylamine. Dependent on the substitution pattern of the starting material one obtains C,C- or C,O- coupling products. These represent the new ring system of trioxabicyclo[3.2.1]octenes 3, which react with electrophiles and nucleophiles yielding tricyclic systems, whereas under hydrolytic conditions furans 14 may result.
关于三酰基甲烷的阳极脱氢二聚:取代的 4,7,8-三氧杂双环[3.2.1]辛烯 ß-三羰基化合物 1 的合成和反应可以在含有一些三乙胺的乙腈中进行阳极氧化。根据起始材料的取代模式,可以获得C,C-或C,O-偶联产物。这些代表三氧杂双环[3.2.1]辛烯3的新环系,其与亲电子试剂和亲核试剂反应产生三环系统,而在水解条件下可能产生呋喃14。