The DOI matches its Crossref record; 17 of the 17 references it cites were found in a registry or an index.
Quantitative characterization of the global electrophilicity power of common diene/dienophile pairs in Diels–Alder reactions
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Citations
Cites
Density-functional thermochemistry. III. The role of exact exchange
Becke, A. D. (1993) · The Journal of Chemical Physics · doi:10.1063/1.464913 · Cited by 103,767
Lee, C., Yang, W., & Parr, R. G. (1988) · Physical Review B · doi:10.1103/physrevb.37.785 · Cited by 100,874
Intermolecular interactions from a natural bond orbital, donor-acceptor viewpoint
Reed, A. E., Curtiss, L. A., & Weinhold, F. (1988) · Chemical Reviews · doi:10.1021/cr00088a005 · Cited by 17,359
Density-functional theory of atoms and molecules
Patterson, J. D. (1989) · Annals of Nuclear Energy · doi:10.1016/0306-4549(89)90016-9 · Cited by 12,545
Density Functional Theory of Atoms and Molecules
Parr, R. G. (1980) · Horizons of Quantum Chemistry · doi:10.1007/978-94-009-9027-2_2 · Cited by 11,964
Reed, A. E., Weinstock, R. B., & Weinhold, F. (1985) · The Journal of Chemical Physics · doi:10.1063/1.449486 · Cited by 9,925
Absolute hardness: companion parameter to absolute electronegativity
Parr, R. G., & Pearson, R. G. (1983) · Journal of the American Chemical Society · doi:10.1021/ja00364a005 · Cited by 7,910
Parr, R. G., Szentpály, L. V., & Liu, S. (1999) · Journal of the American Chemical Society · doi:10.1021/ja983494x · Cited by 7,465
The Conservation of Orbital Symmetry
Woodward, R. B., & Hoffmann, R. (1969) · Angewandte Chemie International Edition in English · doi:10.1002/anie.196907811 · Cited by 4,090
Chemical reactivity and the concept of charge- and frontier-controlled reactions
Klopman, G. (1968) · Journal of the American Chemical Society · doi:10.1021/ja01004a002 · Cited by 1,546
Cited by
Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry Reactivity
Domingo, L., Ríos-Gutiérrez, M., & Pérez, P. (2016) · Molecules · doi:10.3390/molecules21060748 · Cited by 1,304
Self-citationEss, D. H., Jones, G. O., & Houk, K. N. (2006) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200600431 · Cited by 285
Metadata
- Authors
- Domingo, L. R., Aurell, M. J., Pérez, P., & Contreras, R.
- Venue
- Tetrahedron
- Publisher
- Elsevier BV
- Published
- 2002-05
- Volume
- 58
- Issue
- 22
- Pages
- 4417-4423
- ISSN
- 0040-4020 (ISSN-L)
- OpenAlex
- W2011241123
- Cited by
- 1,075
- References
- 17
- FWCI
- 10.51
- Type
- journal article
- Language
- en
- Open access
- green
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- The paper
- Domingo, L. R., Aurell, M. J., Pérez, P., & Contreras, R. (2002). Quantitative characterization of the global electrophilicity power of common diene/dienophile pairs in Diels–Alder reactions. Tetrahedron. https://doi.org/10.1016/s0040-4020(02)00410-6
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
