Pure and Applied Chemistry, 2013, Volume 85, No. 5, pp. 921-940, Cited by

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

http://dx.doi.org/10.1351/PAC-CON-13-01-03

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

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. <http://dx.doi.org/10.1002/poc.3269>
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. <http://dx.doi.org/10.1021/ja4106489>
Lodewyk Michael W., Willenbring Dan, Tantillo Dean J.: Pentalenene formation mechanisms redux. Org. Biomol. Chem. 2014, 12, 887. <http://dx.doi.org/10.1039/c3ob42005a>
Wu Judy I.-Chia, von Rague Schleyer Paul: ChemInform Abstract: Hyperconjugation in Hydrocarbons: Not Just a “Mild Sort of Conjugation”. ChemInform 2013, 44, no. <http://dx.doi.org/10.1002/chin.201349276>