This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2006, 2, No. 26, doi:10.1186/1860-5397-2-26
Graphical Abstract
Figure 1: Bicyclic quinones explored for the transannular interaction.
Figure 2: Conformation A of compound 2.
Figure 3: Conformation B of compound 2.
Figure 4: First formal redox-potentials of compounds 1–5 vs. their calculated LUMO energies.
Figure 5: First formal redox-potentials of compounds 1–5 vs. their calculated energies of reduction.
Figure 6: Second formal redox-potentials of compounds 1–5 vs. their calculated LUMO+1 energies.
Figure 7: LUMO of Compound 1.
Figure 8: LUMO+1 of Compound 1.
Figure 9: LUMO of Compound 2.
Figure 10: LUMO+1 of Compound 2.
Figure 11: LUMO of Compound 4.
Figure 12: LUMO+1 of Compound 4.
Figure 13: LUMO of Compound 5.
Figure 14: LUMO+1 of Compound 5.
Figure 15: LUMO of the reduced species 5·−.
Figure 16: CV for p-benzoquinone and quinone 3.