作者:Toshihide Hatsui、Nobumasa Suzuki、Hitoshi Takeshita
DOI:10.1246/cl.1985.639
日期:1985.5.5
9,10-Dicyanoanthracene-sensitized photooxygenation of thujopsene proceeded by singlet oxygen, but the reaction with added biphenyl caused an electron transfer and produced a novel product which has no longer possessed the cyclopropane ring. The ring cleavage is best explained in terms of intermediary formation of a radical cation.
9,10-二氰基蒽敏化thujopsene的光氧化由单线态氧进行,但与加入的联苯反应引起电子转移并产生不再具有环丙烷环的新产物。环裂解最好用自由基阳离子的中间形成来解释。