Cubane (English Wikipedia)

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

Last modified: 19:41:02, 29 August 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

2922doi.org

2^nd place

1814adsabs.harvard.edu

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116nih.gov

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106worldcat.org

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75ic.ac.uk

low place

75web.archive.org

1^st place

63semanticscholar.org

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8^th place

41nsf.gov

3,608^th place

2,387^th place

22books.google.com

3^rd place

22archive.org

6^th place

11dtic.mil

934^th place

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11wiley.com

150^th place

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11acs.org

865^th place

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11compchemhighlights.org

low place

11hal.science

2,005^th place

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11nature.com

207^th place

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acs.org (Global: 865^th place; English: 887^th place)

pubs.acs.org

Cassar, Luigi; Eaton, Philip E.; Halpern, Jack (1970). "Catalysis of symmetry-restricted reactions by transition metal compounds. Valence isomerization of cubane". Journal of the American Chemical Society. 92 (11): 3515–3518. Bibcode:1970JAChS..92.3515C. doi:10.1021/ja00714a075. ISSN 0002-7863.

adsabs.harvard.edu (Global: 14^th place; English: 9^th place)

ui.adsabs.harvard.edu

Eaton, Philip E.; Cole, Thomas W. (1964). "Cubane". J. Am. Chem. Soc. 86 (15): 3157–3158. Bibcode:1964JAChS..86.3157E. doi:10.1021/ja01069a041.
Wiesenfeldt, Mario P.; Rossi-Ashton, James A.; Perry, Ian B.; Diesel, Johannes; Garry, Olivia L.; Bartels, Florian; Coote, Susannah C.; Ma, Xiaoshen; Yeung, Charles S.; Bennett, David J.; MacMillan, David W. C. (June 2023). "General access to cubanes as benzene bioisosteres". Nature. 618 (7965): 513–518. Bibcode:2023Natur.618..513W. doi:10.1038/s41586-023-06021-8. ISSN 1476-4687. PMC 10680098. PMID 37015289.
Eaton, Philip E.; Cole, Thomas W. (1964). "The Cubane System". J. Am. Chem. Soc. 86 (5): 962–964. Bibcode:1964JAChS..86..962E. doi:10.1021/ja01059a072.
Eaton, Philip E. (1992). "Cubane: Ausgangsverbindungen für die Chemie der neunziger Jahre und des nächsten Jahrhunderts". Angewandte Chemie (in German). 104 (11): 1447–1462. Bibcode:1992AngCh.104.1447E. doi:10.1002/ange.19921041105.
Cassar, Luigi; Eaton, Philip E.; Halpern, Jack (1970). "Catalysis of symmetry-restricted reactions by transition metal compounds. Valence isomerization of cubane". Journal of the American Chemical Society. 92 (11): 3515–3518. Bibcode:1970JAChS..92.3515C. doi:10.1021/ja00714a075. ISSN 0002-7863.
Pichierri, F. (2014). "Hypercubane: DFT-based prediction of an O_h-symmetric double-shell hydrocarbon". Chem. Phys. Lett. 612: 198–202. Bibcode:2014CPL...612..198P. doi:10.1016/j.cplett.2014.08.032.
Freedman, H. H. (1961). "Tetraphenylcyclobutadiene Derivatives. II.1 Chemical Evidence for the Triplet State". J. Am. Chem. Soc. 83 (9): 2195–2196. Bibcode:1961JAChS..83.2195F. doi:10.1021/ja01470a037.
Freedman, H. H.; Petersen, D. R. (1962). "Tetraphenylcyclobutadiene Derivatives. IV.1 "Octaphenylcubane"; A Dimer of Tetraphenylcyclobutadiene". J. Am. Chem. Soc. 84 (14): 2837–2838. Bibcode:1962JAChS..84.2837F. doi:10.1021/ja00873a046.
Pawley, G. S.; Lipscomb, W. N.; Freedman, H. H. (1964). "Structure of the Dimer of tetraphenylcyclobutadiene". J. Am. Chem. Soc. 86 (21): 4725–4726. Bibcode:1964JAChS..86.4725P. doi:10.1021/ja01075a042.
Sugiyama M, Akiyama M, Yonezawa Y, Komaguchi K, Higashi M, Nozaki K, Okazoe T (August 2022). "Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptor". Science. 377 (6607): 756–759. Bibcode:2022Sci...377..756S. doi:10.1126/science.abq0516. PMID 35951682. S2CID 251515925.
Krafft MP, Riess JG (August 2022). "Perfluorocubane-a tiny electron guzzler". Science. 377 (6607): 709. Bibcode:2022Sci...377..709K. doi:10.1126/science.adc9195. PMID 35951708. S2CID 251517529.
Eaton, Philip E.; Maggini, Michele (1988). "Cubene (1,2-dehydrocubane)". J. Am. Chem. Soc. 110 (21): 7230–7232. Bibcode:1988JAChS.110.7230E. doi:10.1021/ja00229a057.
Gilardi, Richard.; Maggini, Michele.; Eaton, Philip E. (1 October 1988). "X-ray structures of cubylcubane and 2-tert-butylcubylcubane: short cage-cage bonds". Journal of the American Chemical Society. 110 (21): 7232–7234. Bibcode:1988JAChS.110.7232G. doi:10.1021/ja00229a058. ISSN 0002-7863.
Huang, Haw-Tyng; Zhu, Li; Ward, Matthew D.; Wang, Tao; Chen, Bo; Chaloux, Brian L.; Wang, Qianqian; Biswas, Arani; Gray, Jennifer L.; Kuei, Brooke; Cody, George D.; Epshteyn, Albert; Crespi, Vincent H.; Badding, John V.; Strobel, Timothy A. (21 January 2020). "Nanoarchitecture through Strained Molecules: Cubane-Derived Scaffolds and the Smallest Carbon Nanothreads". Journal of the American Chemical Society. 142 (42): 17944–17955. Bibcode:2020JAChS.14217944H. doi:10.1021/jacs.9b12352. ISSN 0002-7863. PMID 31961671. S2CID 210870993.

archive.org (Global: 6^th place; English: 6^th place)

Smith, Michael B.; March, Jerry (2001). March's Advanced Organic Chemistry (5th ed.). John Wiley & Sons. p. 1459. ISBN 0-471-58589-0.
Minyaev, Ruslan M.; Minkin, Vladimir I.; Gribanova, Tatyana N. (2009). "2.3 A Theoretical Approach to the Study and Design of Prismane Systems". In Dodziuk, Helena (ed.). Strained Hydrocarbons. Wiley. p. 55. ISBN 9783527627141.

books.google.com (Global: 3^rd place; English: 3^rd place)

Teachers, University of New South Wales Summer School for Chemistry (1963). Approach to Chemistry: Lectures and Workshop Reports of the ... Summer School for Chemistry Teachers. The University. p. 98. "This compound was described only a few months ago and, curiously enough, it is quite easy to make, although only a year ago I would have predicted that it would be difficult, or even impossible, to synthesize."
Moore, John W.; Stanitski, Conrad L.; Jurs, Peter C. (2002). Chemistry: The Molecular Science. Harcourt College Publishers. p. 372. ISBN 978-0-03-032011-8. "This sharp bond angle creates severe bond strain in cubane, a compound thought previously impossible to synthesize because of the required 90° bond angles."

compchemhighlights.org (Global: low place; English: low place)

"Hypercubane: DFT-based prediction of an Oh-symmetric double-shell hydrocarbon".

doi.org (Global: 2^nd place; English: 2^nd place)

Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 169. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. The retained names adamantane and cubane are used in general nomenclature and as preferred IUPAC names.
Biegasiewicz, Kyle; Griffiths, Justin; Savage, G. Paul; Tsanakstidis, John; Priefer, Ronny (2015). "Cubane: 50 years later". Chemical Reviews. 115 (14): 6719–6745. doi:10.1021/cr500523x. PMID 26102302.
Eaton, Philip E.; Cole, Thomas W. (1964). "Cubane". J. Am. Chem. Soc. 86 (15): 3157–3158. Bibcode:1964JAChS..86.3157E. doi:10.1021/ja01069a041.
Wiesenfeldt, Mario P.; Rossi-Ashton, James A.; Perry, Ian B.; Diesel, Johannes; Garry, Olivia L.; Bartels, Florian; Coote, Susannah C.; Ma, Xiaoshen; Yeung, Charles S.; Bennett, David J.; MacMillan, David W. C. (June 2023). "General access to cubanes as benzene bioisosteres". Nature. 618 (7965): 513–518. Bibcode:2023Natur.618..513W. doi:10.1038/s41586-023-06021-8. ISSN 1476-4687. PMC 10680098. PMID 37015289.
Eaton, Philip E.; Cole, Thomas W. (1964). "The Cubane System". J. Am. Chem. Soc. 86 (5): 962–964. Bibcode:1964JAChS..86..962E. doi:10.1021/ja01059a072.
Bliese, Marianne; Tsanaktsidis, John (1997). "Dimethyl Cubane-1,4-dicarboxylate: A Practical Laboratory Scale Synthesis". Australian Journal of Chemistry. 50 (3): 189. doi:10.1071/C97021.
Eaton, Philip E. (1992). "Cubane: Ausgangsverbindungen für die Chemie der neunziger Jahre und des nächsten Jahrhunderts". Angewandte Chemie (in German). 104 (11): 1447–1462. Bibcode:1992AngCh.104.1447E. doi:10.1002/ange.19921041105.
Kindler, K.; Lührs, K. (1966). "Studien über den Mechanismus chemischer Reaktionen, XXIII. Hydrierungen von Nitrilen unter Verwendung von Terpenen als Wasserstoffdonatoren". Chem. Ber. 99: 227–232. doi:10.1002/cber.19660990135.
Cassar, Luigi; Eaton, Philip E.; Halpern, Jack (1970). "Catalysis of symmetry-restricted reactions by transition metal compounds. Valence isomerization of cubane". Journal of the American Chemical Society. 92 (11): 3515–3518. Bibcode:1970JAChS..92.3515C. doi:10.1021/ja00714a075. ISSN 0002-7863.
Bashir-Hashemi, A.; Gelber, Nathan; Gilardi, Richard (1997). "Norcubanes from Cubanes: Novel reactions of amidocubanes with oxalyl chloride". Tetrahedron Letters. 38 (47). Pergamon (Elsevier): 8137–8140. doi:10.1016/S0040-4039(97)10185-X.
Pichierri, F. (2014). "Hypercubane: DFT-based prediction of an O_h-symmetric double-shell hydrocarbon". Chem. Phys. Lett. 612: 198–202. Bibcode:2014CPL...612..198P. doi:10.1016/j.cplett.2014.08.032.
Freedman, H. H. (1961). "Tetraphenylcyclobutadiene Derivatives. II.1 Chemical Evidence for the Triplet State". J. Am. Chem. Soc. 83 (9): 2195–2196. Bibcode:1961JAChS..83.2195F. doi:10.1021/ja01470a037.
Freedman, H. H.; Petersen, D. R. (1962). "Tetraphenylcyclobutadiene Derivatives. IV.1 "Octaphenylcubane"; A Dimer of Tetraphenylcyclobutadiene". J. Am. Chem. Soc. 84 (14): 2837–2838. Bibcode:1962JAChS..84.2837F. doi:10.1021/ja00873a046.
Pawley, G. S.; Lipscomb, W. N.; Freedman, H. H. (1964). "Structure of the Dimer of tetraphenylcyclobutadiene". J. Am. Chem. Soc. 86 (21): 4725–4726. Bibcode:1964JAChS..86.4725P. doi:10.1021/ja01075a042.
Sugiyama M, Akiyama M, Yonezawa Y, Komaguchi K, Higashi M, Nozaki K, Okazoe T (August 2022). "Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptor". Science. 377 (6607): 756–759. Bibcode:2022Sci...377..756S. doi:10.1126/science.abq0516. PMID 35951682. S2CID 251515925.
Pichierri, F. Substituent effects in cubane and hypercubane: a DFT and QTAIM study. Theor Chem Acc 2017; 136: 114. doi:10.1007/s00214-017-2144-5
Krafft MP, Riess JG (August 2022). "Perfluorocubane-a tiny electron guzzler". Science. 377 (6607): 709. Bibcode:2022Sci...377..709K. doi:10.1126/science.adc9195. PMID 35951708. S2CID 251517529.
Eaton, Philip E.; Maggini, Michele (1988). "Cubene (1,2-dehydrocubane)". J. Am. Chem. Soc. 110 (21): 7230–7232. Bibcode:1988JAChS.110.7230E. doi:10.1021/ja00229a057.
Ding, Jiaming; French, Sarah A.; Rivera, Christina A.; Tena Meza, Arismel; Witkowski, Dominick C.; Houk, K. N.; Garg, Neil K. (2026-01-21). "Hyperpyramidalized alkenes with bond orders near 1.5 as synthetic building blocks". Nature Chemistry: 1–10. doi:10.1038/s41557-025-02055-9. ISSN 1755-4349.
Eaton, Philip E. (1992). "Cubanes: Starting Materials for the Chemistry of the 1990s and the New Century". Angewandte Chemie International Edition in English. 31 (11): 1421–1436. doi:10.1002/anie.199214211. ISSN 1521-3773.
Gilardi, Richard.; Maggini, Michele.; Eaton, Philip E. (1 October 1988). "X-ray structures of cubylcubane and 2-tert-butylcubylcubane: short cage-cage bonds". Journal of the American Chemical Society. 110 (21): 7232–7234. Bibcode:1988JAChS.110.7232G. doi:10.1021/ja00229a058. ISSN 0002-7863.
Huang, Haw-Tyng; Zhu, Li; Ward, Matthew D.; Wang, Tao; Chen, Bo; Chaloux, Brian L.; Wang, Qianqian; Biswas, Arani; Gray, Jennifer L.; Kuei, Brooke; Cody, George D.; Epshteyn, Albert; Crespi, Vincent H.; Badding, John V.; Strobel, Timothy A. (21 January 2020). "Nanoarchitecture through Strained Molecules: Cubane-Derived Scaffolds and the Smallest Carbon Nanothreads". Journal of the American Chemical Society. 142 (42): 17944–17955. Bibcode:2020JAChS.14217944H. doi:10.1021/jacs.9b12352. ISSN 0002-7863. PMID 31961671. S2CID 210870993.

dtic.mil (Global: 934^th place; English: 530^th place)

apps.dtic.mil

Fluorochem, Inc (July 1989). "Cubane Derivatives for Propellant Applications" (PDF). Archived (PDF) from the original on 2021-07-09.

hal.science (Global: 2,005^th place; English: 1,689^th place)

Krafft MP, Riess JG (August 2022). "Perfluorocubane-a tiny electron guzzler". Science. 377 (6607): 709. Bibcode:2022Sci...377..709K. doi:10.1126/science.adc9195. PMID 35951708. S2CID 251517529.

ic.ac.uk (Global: low place; English: low place)

ch.ic.ac.uk

"Start".
Muir, B. "Reactivity". Cubane. Imperial College London. Archived from the original on 19 Jan 2024. Retrieved 22 May 2025.
Muir, B. "Properties". Cubane. Imperial College London. The nature of the C–H bond. Archived from the original on 19 Jan 2024. Retrieved 22 May 2025.
Muir, B. "Further topics". Cubane. Imperial College London. Archived from the original on 19 January 2024. Retrieved 22 May 2025.
Muir, B. "Applications". Cubane. Imperial College London. Polymers. Archived from the original on 8 May 2024. Retrieved 22 May 2025.

nature.com (Global: 207^th place; English: 347^th place)

Ding, Jiaming; French, Sarah A.; Rivera, Christina A.; Tena Meza, Arismel; Witkowski, Dominick C.; Houk, K. N.; Garg, Neil K. (2026-01-21). "Hyperpyramidalized alkenes with bond orders near 1.5 as synthetic building blocks". Nature Chemistry: 1–10. doi:10.1038/s41557-025-02055-9. ISSN 1755-4349.

nih.gov (Global: 5^th place; English: 5^th place)

pubmed.ncbi.nlm.nih.gov

Biegasiewicz, Kyle; Griffiths, Justin; Savage, G. Paul; Tsanakstidis, John; Priefer, Ronny (2015). "Cubane: 50 years later". Chemical Reviews. 115 (14): 6719–6745. doi:10.1021/cr500523x. PMID 26102302.
Wiesenfeldt, Mario P.; Rossi-Ashton, James A.; Perry, Ian B.; Diesel, Johannes; Garry, Olivia L.; Bartels, Florian; Coote, Susannah C.; Ma, Xiaoshen; Yeung, Charles S.; Bennett, David J.; MacMillan, David W. C. (June 2023). "General access to cubanes as benzene bioisosteres". Nature. 618 (7965): 513–518. Bibcode:2023Natur.618..513W. doi:10.1038/s41586-023-06021-8. ISSN 1476-4687. PMC 10680098. PMID 37015289.
Sugiyama M, Akiyama M, Yonezawa Y, Komaguchi K, Higashi M, Nozaki K, Okazoe T (August 2022). "Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptor". Science. 377 (6607): 756–759. Bibcode:2022Sci...377..756S. doi:10.1126/science.abq0516. PMID 35951682. S2CID 251515925.
Krafft MP, Riess JG (August 2022). "Perfluorocubane-a tiny electron guzzler". Science. 377 (6607): 709. Bibcode:2022Sci...377..709K. doi:10.1126/science.adc9195. PMID 35951708. S2CID 251517529.
Huang, Haw-Tyng; Zhu, Li; Ward, Matthew D.; Wang, Tao; Chen, Bo; Chaloux, Brian L.; Wang, Qianqian; Biswas, Arani; Gray, Jennifer L.; Kuei, Brooke; Cody, George D.; Epshteyn, Albert; Crespi, Vincent H.; Badding, John V.; Strobel, Timothy A. (21 January 2020). "Nanoarchitecture through Strained Molecules: Cubane-Derived Scaffolds and the Smallest Carbon Nanothreads". Journal of the American Chemical Society. 142 (42): 17944–17955. Bibcode:2020JAChS.14217944H. doi:10.1021/jacs.9b12352. ISSN 0002-7863. PMID 31961671. S2CID 210870993.

ncbi.nlm.nih.gov

Wiesenfeldt, Mario P.; Rossi-Ashton, James A.; Perry, Ian B.; Diesel, Johannes; Garry, Olivia L.; Bartels, Florian; Coote, Susannah C.; Ma, Xiaoshen; Yeung, Charles S.; Bennett, David J.; MacMillan, David W. C. (June 2023). "General access to cubanes as benzene bioisosteres". Nature. 618 (7965): 513–518. Bibcode:2023Natur.618..513W. doi:10.1038/s41586-023-06021-8. ISSN 1476-4687. PMC 10680098. PMID 37015289.

nsf.gov (Global: 3,608^th place; English: 2,387^th place)

par.nsf.gov

Huang, Haw-Tyng; Zhu, Li; Ward, Matthew D.; Wang, Tao; Chen, Bo; Chaloux, Brian L.; Wang, Qianqian; Biswas, Arani; Gray, Jennifer L.; Kuei, Brooke; Cody, George D.; Epshteyn, Albert; Crespi, Vincent H.; Badding, John V.; Strobel, Timothy A. (21 January 2020). "Nanoarchitecture through Strained Molecules: Cubane-Derived Scaffolds and the Smallest Carbon Nanothreads". Journal of the American Chemical Society. 142 (42): 17944–17955. Bibcode:2020JAChS.14217944H. doi:10.1021/jacs.9b12352. ISSN 0002-7863. PMID 31961671. S2CID 210870993.

semanticscholar.org (Global: 15^th place; English: 8^th place)

api.semanticscholar.org

Sugiyama M, Akiyama M, Yonezawa Y, Komaguchi K, Higashi M, Nozaki K, Okazoe T (August 2022). "Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptor". Science. 377 (6607): 756–759. Bibcode:2022Sci...377..756S. doi:10.1126/science.abq0516. PMID 35951682. S2CID 251515925.
Krafft MP, Riess JG (August 2022). "Perfluorocubane-a tiny electron guzzler". Science. 377 (6607): 709. Bibcode:2022Sci...377..709K. doi:10.1126/science.adc9195. PMID 35951708. S2CID 251517529.
Huang, Haw-Tyng; Zhu, Li; Ward, Matthew D.; Wang, Tao; Chen, Bo; Chaloux, Brian L.; Wang, Qianqian; Biswas, Arani; Gray, Jennifer L.; Kuei, Brooke; Cody, George D.; Epshteyn, Albert; Crespi, Vincent H.; Badding, John V.; Strobel, Timothy A. (21 January 2020). "Nanoarchitecture through Strained Molecules: Cubane-Derived Scaffolds and the Smallest Carbon Nanothreads". Journal of the American Chemical Society. 142 (42): 17944–17955. Bibcode:2020JAChS.14217944H. doi:10.1021/jacs.9b12352. ISSN 0002-7863. PMID 31961671. S2CID 210870993.

web.archive.org (Global: 1^st place; English: 1^st place)

Fluorochem, Inc (July 1989). "Cubane Derivatives for Propellant Applications" (PDF). Archived (PDF) from the original on 2021-07-09.
Muir, B. "Reactivity". Cubane. Imperial College London. Archived from the original on 19 Jan 2024. Retrieved 22 May 2025.
Muir, B. "Properties". Cubane. Imperial College London. The nature of the C–H bond. Archived from the original on 19 Jan 2024. Retrieved 22 May 2025.
Muir, B. "Further topics". Cubane. Imperial College London. Archived from the original on 19 January 2024. Retrieved 22 May 2025.
Muir, B. "Applications". Cubane. Imperial College London. Polymers. Archived from the original on 8 May 2024. Retrieved 22 May 2025.

wiley.com (Global: 150^th place; English: 174^th place)

onlinelibrary.wiley.com

Eaton, Philip E. (1992). "Cubane: Ausgangsverbindungen für die Chemie der neunziger Jahre und des nächsten Jahrhunderts". Angewandte Chemie (in German). 104 (11): 1447–1462. Bibcode:1992AngCh.104.1447E. doi:10.1002/ange.19921041105.

worldcat.org (Global: 4^th place; English: 4^th place)

search.worldcat.org

Wiesenfeldt, Mario P.; Rossi-Ashton, James A.; Perry, Ian B.; Diesel, Johannes; Garry, Olivia L.; Bartels, Florian; Coote, Susannah C.; Ma, Xiaoshen; Yeung, Charles S.; Bennett, David J.; MacMillan, David W. C. (June 2023). "General access to cubanes as benzene bioisosteres". Nature. 618 (7965): 513–518. Bibcode:2023Natur.618..513W. doi:10.1038/s41586-023-06021-8. ISSN 1476-4687. PMC 10680098. PMID 37015289.
Cassar, Luigi; Eaton, Philip E.; Halpern, Jack (1970). "Catalysis of symmetry-restricted reactions by transition metal compounds. Valence isomerization of cubane". Journal of the American Chemical Society. 92 (11): 3515–3518. Bibcode:1970JAChS..92.3515C. doi:10.1021/ja00714a075. ISSN 0002-7863.
Ding, Jiaming; French, Sarah A.; Rivera, Christina A.; Tena Meza, Arismel; Witkowski, Dominick C.; Houk, K. N.; Garg, Neil K. (2026-01-21). "Hyperpyramidalized alkenes with bond orders near 1.5 as synthetic building blocks". Nature Chemistry: 1–10. doi:10.1038/s41557-025-02055-9. ISSN 1755-4349.
Eaton, Philip E. (1992). "Cubanes: Starting Materials for the Chemistry of the 1990s and the New Century". Angewandte Chemie International Edition in English. 31 (11): 1421–1436. doi:10.1002/anie.199214211. ISSN 1521-3773.
Gilardi, Richard.; Maggini, Michele.; Eaton, Philip E. (1 October 1988). "X-ray structures of cubylcubane and 2-tert-butylcubylcubane: short cage-cage bonds". Journal of the American Chemical Society. 110 (21): 7232–7234. Bibcode:1988JAChS.110.7232G. doi:10.1021/ja00229a058. ISSN 0002-7863.
Huang, Haw-Tyng; Zhu, Li; Ward, Matthew D.; Wang, Tao; Chen, Bo; Chaloux, Brian L.; Wang, Qianqian; Biswas, Arani; Gray, Jennifer L.; Kuei, Brooke; Cody, George D.; Epshteyn, Albert; Crespi, Vincent H.; Badding, John V.; Strobel, Timothy A. (21 January 2020). "Nanoarchitecture through Strained Molecules: Cubane-Derived Scaffolds and the Smallest Carbon Nanothreads". Journal of the American Chemical Society. 142 (42): 17944–17955. Bibcode:2020JAChS.14217944H. doi:10.1021/jacs.9b12352. ISSN 0002-7863. PMID 31961671. S2CID 210870993.

Cubane (English Wikipedia)

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