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| Supporting Information File 2: Copies of 1H and 13C NMR spectra for compounds 3a–l. | ||
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Cite the Following Article
Regioselective palladium-catalyzed ring-opening reactions of C1-substituted oxabicyclo[2,2,1]hepta-2,5-diene-2,3-dicarboxylates
Michael Edmunds, Mohammed Abdul Raheem, Rebecca Boutin, Katrina Tait and William Tam
Beilstein J. Org. Chem. 2016, 12, 239–244.
https://doi.org/10.3762/bjoc.12.25
How to Cite
Edmunds, M.; Raheem, M. A.; Boutin, R.; Tait, K.; Tam, W. Beilstein J. Org. Chem. 2016, 12, 239–244. doi:10.3762/bjoc.12.25
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Scholarly Works
- Pounder, A.; King, N.; Tam, W. Ruthenium‐Catalyzed Isomerization of Oxabicyclic Alkenes to 1,2‐Naphthalene Oxides: A Density Functional Theory Study. European Journal of Organic Chemistry 2025, 28. doi:10.1002/ejoc.202500192
- Lough, A. J.; Ho, A.; Tam, W. [(1R*,3S*,4S*)-3-(2-Hydroxybenzoyl)-1,2,3,4-tetrahydro-1,4-epoxynaphthalen-1-yl]methyl 4-nitrobenzoate. IUCrData 2020, 5, x200265. doi:10.1107/s2414314620002655
- Wicks, C.; Koh, S.; Pounder, A.; Carlson, E.; Tam, W. Acid-catalyzed intramolecular ring-opening reactions of cyclopropanated oxabenzonorbornadienes with alcohol nucleophiles. Tetrahedron Letters 2019, 60, 151228. doi:10.1016/j.tetlet.2019.151228
- Boutin, R.; Koh, S.; Tam, W. Recent Advances in Transition Metal-Catalyzed Reactions of Oxabenzonorbornadiene. Current organic synthesis 2019, 16, 460–484. doi:10.2174/1570179416666181122094643
- Lough, A. J.; Hill, J.; Tam, W. 1-[(1R*,2R*)-1,2-Dihydroxy-1,2-dihydronaphthalen-1-yl]ethan-1-one. IUCrData 2019, 4. doi:10.1107/s2414314619006096
- Edmunds, M.; Raheem, M. A.; Boutin, R.; Tait, K.; Tam, W. Regioselective Palladium-Catalyzed Ring-Opening Reactions of C1-Substituted Oxabicyclo[2,2,1]hepta-2,5-diene-2,3-dicarboxylates. ChemInform 2016, 47. doi:10.1002/chin.201621129
