作者:Kenneth B. Wiberg、John R. Snoonian、Paul M. Lahti
DOI:10.1016/0040-4039(96)01938-7
日期:1996.11
The diazoketone derived from tricyclo[4.1.0.01,3]heptan-4-one on photolysis in dimethylamine leads to a novel product that appears to be formed via a cyclopropylcarbene rearrangement followed by dimethylamine addition and the cleavage of one of the cyclobutane rings. In a matrix at 15K, photolysis led to the loss of the 2085 cm−1 diazo band and the formation of a new band at 2117 cm−1 which is characteristic
在二甲胺中光解时,由三环[4.1.0.0 1,3 ]庚烷-4-酮衍生的重氮酮可导致形成一种新产物,该产物似乎是通过环丙基卡宾重排,随后加入二甲胺和裂解一个环丁烷环而形成的。在15K的基质中,光解导致2085 cm -1的重氮带丢失,并在2117 cm -1处形成新的带,这是小环烯酮(如环丙基烯酮)的特征。