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Pure Appl. Chem., 2013, Vol. 85, No. 5, pp. 921-940

Published online 2013-04-29

Hyperconjugation in hydrocarbons: Not just a “mild sort of conjugation”*

Judy I-Chia Wu* and Paul von Ragué Schleyer

Department of Chemistry, Center for Computational Quantum Chemistry, University of Georgia, Athens, GA 30602, USA

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  • Roth Heinz D., Sauers Ronald R., Theisen Kevin J., Neshchadin Dmytro, Gescheidt Georg: Radical cations of disubstituted cyclopropanes: stereoelectronic effects on hyperfine coupling. J. Phys. Org. Chem. 2014, 27, 218. <>
  • Hong Young J., Tantillo Dean J.: Branching Out from the Bisabolyl Cation. Unifying Mechanistic Pathways to Barbatene, Bazzanene, Chamigrene, Chamipinene, Cumacrene, Cuprenene, Dunniene, Isobazzanene, Iso-γ-bisabolene, Isochamigrene, Laurene, Microbiotene, Sesquithujene, Sesquisabinene, Thujopsene, Trichodiene, and Widdradiene Sesquiterpenes. J. Am. Chem. Soc. 2014, 136, 2450. <>
  • Lodewyk Michael W., Willenbring Dan, Tantillo Dean J.: Pentalenene formation mechanisms redux. Org. Biomol. Chem. 2014, 12, 887. <>
  • Wu Judy I.-Chia, von Rague Schleyer Paul: ChemInform Abstract: Hyperconjugation in Hydrocarbons: Not Just a “Mild Sort of Conjugation”. ChemInform 2013, 44, no. <>