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Beilstein J. Org. Chem. 2017, 13, 1669–1669, doi:10.3762/bjoc.13.161
Figure 1: Corrected Figure 6 of the original article. The portion of the norborn-2-en-7-ylmethyl cation PES e...
Beilstein J. Org. Chem. 2016, 12, 377–390, doi:10.3762/bjoc.12.41
Graphical Abstract
Figure 1: Representative terpenes.
Figure 2: Two different models showing how energy evolves throughout the course of a reaction: (a) a two-dime...
Figure 3: A depiction of the “snowboarder” analogy for reactions displaying non-statistical dynamic effects. ...
Figure 4: The tetramethylbromonium ion system [14].
Figure 5: The reaction mechanisms of interest in the PES and dynamics studies of Dupuis and co-workers (R = CH...
Figure 6: The portion of the norborn-2-en-7-ylmethyl cation PES examined by Ghigo et al. [60]. Energies reported ...
Figure 7: The transformation of 2-norbornyl cation to 1,3-dimethylcyclopentyl cation.
Figure 8: Carbocation rearrangements for which trajectory calculations were used to estimate lifetimes of sec...
Figure 9: Carbocation rearrangements involved in abietadiene formation.
Figure 10: Carbocation rearrangements involved in miltiradiene formation.
Figure 11: Top: carbocation rearrangements involved in epi-isozizaene formation. Bottom: reaction coordinate d...