We investigated the site selectivity switch in BF3-catalyzed dual skeletal rearrangements of cyclobutene-fused diarylhomobenzoquinones by changing the stoichiometric amount of acid concentration. From
The datasets included in this submission include the calculations carried out for an optimization study. They also include the raw mass loss vs time data for a large number of kinetic studies carried
Numerical data on coulomb-corrected strong field approximation for hydrogen datalai provided by Lai (see file name for association to figures and figure description in the published work),
