Wu, Judy I.

Aromaticity: Quo Vadis

Merino, G., Solà, M., Fernández, I., Foroutan-Nejad, C., Lazzeretti, P., Frenking, G., Anderson, H. L., Sundholm, D., Cossío, F. P., Petrukhina, M. A., et al. (2023) · Chemical Science

Synthesis and Properties of Aromatic CompoundsCyclization and Aryne Chemistry

Cited by 210

Excited-state proton transfer relieves antiaromaticity in molecules

Wu, C.-H., Karas, L. J., Ottosson, H., & Wu, J. I.-C. (2019) · Proceedings of the National Academy of Sciences

Photochemistry and Electron Transfer StudiesPhotolysis and Reactive Intermediates

Cited by 110

Is cyclobutadiene really highly destabilized by antiaromaticity?

Wu, J. I.-C., Mo, Y., Evangelista, F. A., & von Ragué Schleyer, P. (2012) · Chemical Communications

Synthesis and Properties of Aromatic CompoundsOrganic Chemistry Cycloaddition Reactions

Cited by 85

Why Cyclooctatetraene Is Highly Stabilized: The Importance of “Two-Way” (Double) Hyperconjugation

Wu, J. I., Fernández, I., Mo, Y., & Schleyer, P. V. R. (2012) · Journal of Chemical Theory and Computation

Synthesis and Properties of Aromatic CompoundsAdvanced Chemical Physics Studies

Cited by 58

Electron-driven proton transfer relieves excited-state antiaromaticity in photoexcited DNA base pairs

Karas, L. J., Wu, C.-H., Ottosson, H., & Wu, J. I. (2020) · Chemical Science

Photochemistry and Electron Transfer StudiesDNA and Nucleic Acid Chemistry

Cited by 41