Siklooktatetraen (Uzbek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Siklooktatetraen" in Uzbek language version.

refsWebsite

Global rank Uzbek rank

19doi.org

2^nd place

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5harvard.edu

18^th place

35^th place

3nih.gov

4^th place

7^th place

1zenodo.org

621^st place

872^nd place

1jstor.org

26^th place

78^th place

1acs.org

1,248^th place

1,669^th place

1jst.go.jp

1,903^rd place

4,282^nd place

1web.archive.org

1^st place

acs.org

pubs.acs.org

Zimmerman, H. E.; Grunewald, G. L. (1966). „The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene“ (PDF). J. Am. Chem. Soc. 88-jild, № 1. 183–184-bet. doi:10.1021/ja00953a045.

doi.org

Mason, S. (February 1997). „The Science and Humanism of Linus Pauling (1901−1994)“. Chem. Soc. Rev. 26-jild. 29–39-bet. doi:10.1039/CS9972600029.
Richard Willstätter; Ernst Waser (1911). „Über Cyclo-octatetraen“. Berichte der Deutschen Chemischen Gesellschaft. 44-jild, № 3. 3423–3445-bet. doi:10.1002/cber.191104403216. {{cite magazine}}: Unknown parameter |trans_title= ignored (|trans-title= suggested) (yordam)
Reppe, Walter; Schlichting, Otto; Klager, Karl; Toepel, Tim (1948). „Cyclisierende Polymerisation von Acetylen. I. Über Cyclooctatetraen“. Justus Liebigs Annalen der Chemie. 560-jild, № 1. 1–92-bet. doi:10.1002/jlac.19485600102. {{cite magazine}}: Unknown parameter |trans_title= ignored (|trans-title= suggested) (yordam)
Cope, Arthur C.; Overberger, C. G. (1947). „The synthesis of cycloöctatetraene from pseudopelletierine“. Journal of the American Chemical Society. 69-jild, № 4. 976-bet. doi:10.1021/ja01196a513. PMID 20292490.
Cope, Arthur C.; Overberger, C. G. (1947). „Cyclic Polyolefins. I. Synthesis of Cycloöctatetraene from Pseudopelletierine“. Journal of the American Chemical Society. 70-jild, № 4. 1433–1437-bet. doi:10.1021/ja01184a041. PMID 18915758.
Bastiensen, O.; Hassel, O.; Langseth, A. (1947). „The 'Octa-Benzene', Cyclo-octatetraene (C₈H₈)“. Nature. 160-jild, № 4056. 128-bet. Bibcode:1947Natur.160..128B. doi:10.1038/160128a0.
Kaufman, H. S.; Fankuchen, I.; H., Mark (1948). „Structure of Cyclo-octatetraene“. Nature. 161-jild, № 4083. 165-bet. Bibcode:1948Natur.161..165K. doi:10.1038/161165a0.
Thomas, P. M.; Weber, A. (1978). „High resolution Raman spectroscopy of gases with laser sources. XIII – the pure rotational spectra of 1,3,5,7-cyclooctatetraene and 1,5-cyclooctadiene“. J. Raman Spectr. 7-jild, № 6. 353–357-bet. Bibcode:1978JRSp....7..353T. doi:10.1002/jrs.1250070614.
Claus, K. H.; Krüger, C. (15–sentabr 1988–yil). „Structure of cyclooctatetraene at 129 K“. Acta Crystallogr. C. 44-jild, № 9. 1632–1634-bet. doi:10.1107/S0108270188005840.{{cite magazine}}: CS1 maint: date format ()
Nishinaga, Tohru; Ohmae, Takeshi; Iyoda, Masahiko (5–fevral 2010–yil). „Recent Studies on the Aromaticity and Antiaromaticity of Planar Cyclooctatetraene“. Symmetry. 2-jild, № 1. 76–97-bet. Bibcode:2010Symm....2...76N. doi:10.3390/sym2010076.{{cite magazine}}: CS1 maint: date format ()
Zimmerman, H. E.; Grunewald, G. L. (1966). „The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene“ (PDF). J. Am. Chem. Soc. 88-jild, № 1. 183–184-bet. doi:10.1021/ja00953a045.
Wang, C.; Yuan, J.; Li, G.; Wang, Z.; Zhang, S.; Xi, Z. (2006). „Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes“. J. Am. Chem. Soc. 128-jild, № 14. 4564–4565-bet. doi:10.1021/ja0579208. PMID 16594680.
Stinson, M.; Ezra, D.; Hess, W. M.; Sears, J.; Strobel, G. (2003). „An endophytic Gliocladium sp. of Eucryphia cordifolia producing selective volatile antimicrobial compounds“. Plant Sci. 165-jild, № 4. 913–922-bet. doi:10.1016/S0168-9452(03)00299-1.
Moorhead, Eric J.; Wenzel, Anna G. (August 2009). „Two Undergraduate Experiments in Organic Polymers: The Preparation of Polyacetylene and Telechelic Polyacetylene via Ring-Opening Metathesis Polymerization“. Journal of Chemical Education. 86-jild, № 8. 973-bet. Bibcode:2009JChEd..86..973M. doi:10.1021/ed086p973.
Holovka, J. M.; Gardner, P. D.; Strow, C. B.; Hill, M. L.; Van Auken, T. V. (1968). „Photolysis and photoisomerization of cyclooctatetraene oxide“. Journal of the American Chemical Society. 90-jild, № 18. 5041–5043-bet. doi:10.1021/ja01020a058.
Katz, Thomas J. (1960). „The cyclooctatetraenyl dianion“. J. Am. Chem. Soc. 82-jild, № 14. 3784–3785-bet. doi:10.1021/ja01499a077.
Cotton, F. Albert; Hunter, Douglas L. (1976). „Carbon-13 Nuclear Magnetic Resonance Study of the Fluxional Behavior of Cyclooctatetraenetricarbonyliron and -Ruthenium“. Journal of the American Chemical Society. 98-jild, № 6. 1413–1417-bet. doi:10.1021/ja00422a022.
R. Pettit and J. Henery (1970). „cis-dichlorocyclobutene“. Organic Syntheses. 50-jild. 36-bet. doi:10.15227/orgsyn.050.0036.
„CYCLOBUTADIENE IN SYNTHESIS: Endo-TRICYCLO[4.4.0.02,5]DECA-3,8-DIENE-7,10-DIONE“. Organic Syntheses. 55-jild. 1976. 43-bet. doi:10.15227/orgsyn.055.0043.

harvard.edu

ui.adsabs.harvard.edu

Bastiensen, O.; Hassel, O.; Langseth, A. (1947). „The 'Octa-Benzene', Cyclo-octatetraene (C₈H₈)“. Nature. 160-jild, № 4056. 128-bet. Bibcode:1947Natur.160..128B. doi:10.1038/160128a0.
Kaufman, H. S.; Fankuchen, I.; H., Mark (1948). „Structure of Cyclo-octatetraene“. Nature. 161-jild, № 4083. 165-bet. Bibcode:1948Natur.161..165K. doi:10.1038/161165a0.
Thomas, P. M.; Weber, A. (1978). „High resolution Raman spectroscopy of gases with laser sources. XIII – the pure rotational spectra of 1,3,5,7-cyclooctatetraene and 1,5-cyclooctadiene“. J. Raman Spectr. 7-jild, № 6. 353–357-bet. Bibcode:1978JRSp....7..353T. doi:10.1002/jrs.1250070614.
Nishinaga, Tohru; Ohmae, Takeshi; Iyoda, Masahiko (5–fevral 2010–yil). „Recent Studies on the Aromaticity and Antiaromaticity of Planar Cyclooctatetraene“. Symmetry. 2-jild, № 1. 76–97-bet. Bibcode:2010Symm....2...76N. doi:10.3390/sym2010076.{{cite magazine}}: CS1 maint: date format ()
Moorhead, Eric J.; Wenzel, Anna G. (August 2009). „Two Undergraduate Experiments in Organic Polymers: The Preparation of Polyacetylene and Telechelic Polyacetylene via Ring-Opening Metathesis Polymerization“. Journal of Chemical Education. 86-jild, № 8. 973-bet. Bibcode:2009JChEd..86..973M. doi:10.1021/ed086p973.

jst.go.jp

nanostruct-mater.jst.go.jp

„JST Nanostructed Materials Project Highlights – Prof. Nakajima's Presentation“. 2008-yil 19-fevralda asl nusxadan arxivlangan. Qaraldi: 2005-yil 24-noyabr.

jstor.org

Johnson, A. W. (1947). „Organic Chemistry“. Sci. Progr. 35-jild, № 139. 506–515-bet. JSTOR 43413011.

nih.gov

pubmed.ncbi.nlm.nih.gov

Cope, Arthur C.; Overberger, C. G. (1947). „The synthesis of cycloöctatetraene from pseudopelletierine“. Journal of the American Chemical Society. 69-jild, № 4. 976-bet. doi:10.1021/ja01196a513. PMID 20292490.
Cope, Arthur C.; Overberger, C. G. (1947). „Cyclic Polyolefins. I. Synthesis of Cycloöctatetraene from Pseudopelletierine“. Journal of the American Chemical Society. 70-jild, № 4. 1433–1437-bet. doi:10.1021/ja01184a041. PMID 18915758.
Wang, C.; Yuan, J.; Li, G.; Wang, Z.; Zhang, S.; Xi, Z. (2006). „Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes“. J. Am. Chem. Soc. 128-jild, № 14. 4564–4565-bet. doi:10.1021/ja0579208. PMID 16594680.

web.archive.org

„JST Nanostructed Materials Project Highlights – Prof. Nakajima's Presentation“. 2008-yil 19-fevralda asl nusxadan arxivlangan. Qaraldi: 2005-yil 24-noyabr.

zenodo.org

Richard Willstätter; Ernst Waser (1911). „Über Cyclo-octatetraen“. Berichte der Deutschen Chemischen Gesellschaft. 44-jild, № 3. 3423–3445-bet. doi:10.1002/cber.191104403216. {{cite magazine}}: Unknown parameter |trans_title= ignored (|trans-title= suggested) (yordam)