The regioselectivity and siteselectivity of above cycloadditions can be elucidated by FMO theory.
用前线分子轨道(FMO)理论可以说明上述反应的区域选择性与位置选择性。
2
The strong acid is the active site for creaking para-diethylbenzene and ethylbenzene and it has little effect on p-isomer selectivity of disproportionation and isomerization.