A series of monoterpenoids differing in the number of double bonds and the pattern of their substitution were tested in the liquid-phase noncatalytic oxidation with nitrous oxide (N2O). The structure of olefins has a significant effect on the oxidation route. In the case of terpenoids containing 1,1-disubstituted double bond, nor-carbonyl compounds are formed with high selectivity.
一系列在双键数量和取代模式上不同的单
萜类化合物在液相非催化氧化中与
一氧化氮(
N2O)进行了测试。烯烃的结构对氧化路线有显著影响。在包含1,1-二取代双键的
萜类化合物的情况下,具有高选择性地生成诺羰基化合物。