作者:Teruzo Asahara、Katsumichi Ono、Kazuki Tanaka
DOI:10.1246/bcsj.44.1130
日期:1971.4
The pyrolysis reactions of dihalocyclopropanes and monohalocyclopropanes were carried out at 200–400°C. Bromo-substituted cyclopropanes were readily decomposed in this temperature range. In all cases, the pyrolysis products were ring-opened olefinic hydrocarbons. As for the monohalocyclopropanes, the reactions proceed in a stereospecific manner. The possible mechanism was discussed in terms of the
二卤环丙烷和单卤环丙烷的热解反应在 200-400°C 下进行。溴取代的环丙烷在此温度范围内很容易分解。在所有情况下,热解产物都是开环烯烃。至于单卤代环丙烷,反应以立体定向方式进行。根据电环开环的要求讨论了可能的机制。