作者:R.D Miller、W Theis
DOI:10.1016/s0040-4039(00)84552-9
日期:1986.1
The title compound undergoes an unusual thermal cyclobutyl to cyclopentyl rearrangement initiated by the intramolecular reaction of a ketene moiety produced in situ with the pendant functionality.
标题化合物经历不寻常的热环丁基到环戊基的重排,这是由就地产生的具有悬垂官能团的乙烯酮部分的分子内反应引发的。