Antiaromaticity (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Antiaromaticity" in English language version.

refsWebsite

Global rank English rank

14doi.org

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5nih.gov

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3harvard.edu

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3iupac.org

538^th place

863^rd place

2semanticscholar.org

11^th place

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1worldcat.org

5^th place

doi.org

"IUPAC Gold Book: Antiaromaticity". doi:10.1351/goldbook.AT06987. Retrieved 27 October 2013.
Wu, Judy I-Chia; Mo, Yirong; Evangelista, Francesco Alfredo; von Ragué Schleyer, Paul (2012). "Is cyclobutadiene really highly destabilized by antiaromaticity?". Chemical Communications. 48 (67): 8437–9. doi:10.1039/c2cc33521b. ISSN 1359-7345. PMID 22801355. S2CID 19920318.
Breslow, Ronald; Brown, John; Gajewski, Joseph J. (August 1967). "Antiaromaticity of cyclopropenyl anions". Journal of the American Chemical Society. 89 (17): 4383–4390. doi:10.1021/ja00993a023.
Moss, G. P.; Smith, P. A. S.; Tavernier, D. (1995). "Glossary of class names of organic compounds and reactivity intermediates based on structure". Pure and Applied Chemistry. 67: 1307–1375. doi:10.1351/pac199567081307.
Podlogar, Brent L.; William A. Glauser; Walter R. Rodriguez; Douglas J. Raber (1988). "A Conformational Criterion for Aromaticity and Antiaromaticity". Journal of Organic Chemistry. 53 (9): 2127–2129. doi:10.1021/jo00244a059.
Breslow, Ronald (December 1973). "Antiaromaticity". Accounts of Chemical Research. 6 (12): 393–398. doi:10.1021/ar50072a001.
Alkorta, Ibon; Rozas, Isabel; Elguero, Jose (June 1992). "An ab initio study of the NMR properties (absolute shielding and NICS) of a series of significant aromatic and antiaromatic compounds". Tetrahedron. 118 (28): 880–885. doi:10.1016/S0040-4020(01)00585-3.
Jusélius, Jonas; Dage Sundholm (2008). "Polycyclic antiaromatic hydrocarbons". Physical Chemistry Chemical Physics. 10 (44): 6630–6634. Bibcode:2008PCCP...10.6630J. doi:10.1039/b808082h. PMID 18989474. S2CID 8205257.
Liu, Binyao; Wei Shen; Xiaohua Xie; Lidan Deng; Ming Li (August 2011). "Theoretical analysis on geometries and electronic structures of antiaromatic pentalene and its N-substituted derivatives: monomer, oligomers and polymer". Journal of Physical Organic Chemistry. 25 (4): 278–286. doi:10.1002/poc.1907.
Jusélias, Jonas; Dage Sundholm (2001). "The aromaticity and antiaromaticity of dehydroannulenes". Physical Chemistry Chemical Physics. 3 (12): 2433–2437. Bibcode:2001PCCP....3.2433J. doi:10.1039/B101179K.
Wörner HJ; Merkt F (July 2007). "Diradicals, antiaromaticity, and the pseudo-Jahn-Teller effect: electronic and rovibronic structures of the cyclopentadienyl cation". Journal of Chemical Physics. 127 (3): 034303. Bibcode:2007JChPh.127c4303W. doi:10.1063/1.2748049. PMID 17655439.
Yi, Li; K. N. Houk (July 2001). "The Dimerization of Cyclobutadiene. An ab Initio CASSCF Theoretical Study". Journal of the American Chemical Society. 57: 6043–6049. doi:10.1016/S0040-4020(01)00585-3.
Miao, Shaobin (2007). "A Thiadiazole-Fused N , N -Dihydroquinoxaline: Antiaromatic but Isolable". Organic Letters. 9 (6): 1073–1076. doi:10.1021/ol070013i. PMID 17309273.
Lawrence, Anthony J.; Hutchings, Michael G.; Kennedy, Alan R.; McDouall, Joseph J. W. (2010). "Benzodifurantrione: A Stable Phenylogous Enol". Journal of Organic Chemistry. 75 (3): 690–701. doi:10.1021/jo9022155. PMID 20055373.

harvard.edu

ui.adsabs.harvard.edu

Jusélius, Jonas; Dage Sundholm (2008). "Polycyclic antiaromatic hydrocarbons". Physical Chemistry Chemical Physics. 10 (44): 6630–6634. Bibcode:2008PCCP...10.6630J. doi:10.1039/b808082h. PMID 18989474. S2CID 8205257.
Jusélias, Jonas; Dage Sundholm (2001). "The aromaticity and antiaromaticity of dehydroannulenes". Physical Chemistry Chemical Physics. 3 (12): 2433–2437. Bibcode:2001PCCP....3.2433J. doi:10.1039/B101179K.
Wörner HJ; Merkt F (July 2007). "Diradicals, antiaromaticity, and the pseudo-Jahn-Teller effect: electronic and rovibronic structures of the cyclopentadienyl cation". Journal of Chemical Physics. 127 (3): 034303. Bibcode:2007JChPh.127c4303W. doi:10.1063/1.2748049. PMID 17655439.

iupac.org

Moss, G. P.; Smith, P. A. S.; Tavernier, D. (1995). "Glossary of class names of organic compounds and reactivity intermediates based on structure". Pure and Applied Chemistry. 67: 1307–1375. doi:10.1351/pac199567081307.
What is aromaticity? Paul von Ragué Schleyer and Haijun Jiao. Pure and Applied Chemistry. Vol. 68, No. 2, pp. 209-218, 1996 Link

goldbook.iupac.org

"IUPAC Gold Book: Antiaromaticity". doi:10.1351/goldbook.AT06987. Retrieved 27 October 2013.

nih.gov

pubmed.ncbi.nlm.nih.gov

Wu, Judy I-Chia; Mo, Yirong; Evangelista, Francesco Alfredo; von Ragué Schleyer, Paul (2012). "Is cyclobutadiene really highly destabilized by antiaromaticity?". Chemical Communications. 48 (67): 8437–9. doi:10.1039/c2cc33521b. ISSN 1359-7345. PMID 22801355. S2CID 19920318.
Jusélius, Jonas; Dage Sundholm (2008). "Polycyclic antiaromatic hydrocarbons". Physical Chemistry Chemical Physics. 10 (44): 6630–6634. Bibcode:2008PCCP...10.6630J. doi:10.1039/b808082h. PMID 18989474. S2CID 8205257.
Wörner HJ; Merkt F (July 2007). "Diradicals, antiaromaticity, and the pseudo-Jahn-Teller effect: electronic and rovibronic structures of the cyclopentadienyl cation". Journal of Chemical Physics. 127 (3): 034303. Bibcode:2007JChPh.127c4303W. doi:10.1063/1.2748049. PMID 17655439.
Miao, Shaobin (2007). "A Thiadiazole-Fused N , N -Dihydroquinoxaline: Antiaromatic but Isolable". Organic Letters. 9 (6): 1073–1076. doi:10.1021/ol070013i. PMID 17309273.
Lawrence, Anthony J.; Hutchings, Michael G.; Kennedy, Alan R.; McDouall, Joseph J. W. (2010). "Benzodifurantrione: A Stable Phenylogous Enol". Journal of Organic Chemistry. 75 (3): 690–701. doi:10.1021/jo9022155. PMID 20055373.

semanticscholar.org

api.semanticscholar.org

Wu, Judy I-Chia; Mo, Yirong; Evangelista, Francesco Alfredo; von Ragué Schleyer, Paul (2012). "Is cyclobutadiene really highly destabilized by antiaromaticity?". Chemical Communications. 48 (67): 8437–9. doi:10.1039/c2cc33521b. ISSN 1359-7345. PMID 22801355. S2CID 19920318.
Jusélius, Jonas; Dage Sundholm (2008). "Polycyclic antiaromatic hydrocarbons". Physical Chemistry Chemical Physics. 10 (44): 6630–6634. Bibcode:2008PCCP...10.6630J. doi:10.1039/b808082h. PMID 18989474. S2CID 8205257.

worldcat.org

search.worldcat.org

Wu, Judy I-Chia; Mo, Yirong; Evangelista, Francesco Alfredo; von Ragué Schleyer, Paul (2012). "Is cyclobutadiene really highly destabilized by antiaromaticity?". Chemical Communications. 48 (67): 8437–9. doi:10.1039/c2cc33521b. ISSN 1359-7345. PMID 22801355. S2CID 19920318.