シクロプロペニウム (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "シクロプロペニウム" in Japanese language version.

Last modified: 22:24:41, 28 June 2024 (UTC)

Ref.Un. Ref.Website

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1615doi.org

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87nih.gov

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11^th place

22adsabs.harvard.edu

14^th place

60^th place

11books.google.com

3^rd place

40^th place

11pnas.org

1,411^th place

1,422^nd place

11escholarship.org

1,477^th place

3,984^th place

adsabs.harvard.edu (Global: 14^th place; Japanese: 60^th place)

ui.adsabs.harvard.edu

Buchholz, Herwig; Surya Prakash, G. K.; Deffieux, Denis; Olah, George (1999). “Electrochemical preparation of tris(tert-butyldimethylsilyl)cyclopropene and its hydride abstraction to tris(tert-butyldimethylsilyl)cyclopropenium tetrafluoroborate”. Proc. Natl. Acad. Sci. 96 (18): 10003–10005. Bibcode:1999PNAS...9610003B. doi:10.1073/pnas.96.18.10003. PMC 17831. PMID 10468551.
Jiang, Yivan; Freyer, Jessica; Cotanda, Pepa; Brucks, Spencer; Killops, Kato; Bandar, Jeffrey; Torsitano, Christopher; Balsara, Nitash et al. (2015). “The evolution of cyclopropenium ions into functional polyelectrolytes”. Nature Communications 6 (1): 1–7. Bibcode:2015NatCo...6E5950J. doi:10.1038/ncomms6950. PMC 4354017. PMID 25575214.

books.google.com (Global: 3^rd place; Japanese: 40^th place)

Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 0-471-72091-7

doi.org (Global: 2^nd place; Japanese: 3^rd place)

A.Aliab, C.Puzzarinid, "Cyclopropenyl cation – the simplest Huckel's aromatic molecule – and its cyclic methyl derivatives in Titan's upper atmosphere", Planetary and Space Science, Volume 87, October 2013, Pages 96-105. https://doi.org/10.1016/j.pss.2013.07.007
De Meijere, A.; Faber, D.; Noltemeyer, M.; Boese, R.; Haumann, T.; Muller, T.; Bendikov, M.; Matzner, E. et al. (1996). “Tris(trimethylsilyl)cyclopropenylium Cation: The First X-ray Structure Analysis of an α-Silyl-Substituted Carbocation”. J. Org. Chem. 61 (24): 8564. doi:10.1021/jo960478e.
Yadav, Arvind (2012). “Cyclopropenium Ion”. Synlett 23 (16): 2428–2429. doi:10.1055/s-0032-1317230.
Ronald Breslow (1957). “Synthesis of the s-Triphenylcyclopropenyl Cation”. J. Am. Chem. Soc. 79 (19): 5318. doi:10.1021/ja01576a067.
Xu, Ruo; Breslow, Ronald (1997). “1,2,3-Triphenylcyclopropenium Bromide”. Org. Synth. 74: 72. doi:10.15227/orgsyn.074.0072.
Breslow, R.; Groves, J. T. (1970). “Cyclopropenyl Cation. Synthesis and Characterization”. J. Am. Chem. Soc. 92 (4): 984–987. doi:10.1021/ja00707a040.
Glück, C.; Poingée, V.; Schwager, H. (1987). “Improved Synthesis of 7,7-Difluorocyclopropabenzene”. Synthesis 1987 (3): 260–262. doi:10.1055/s-1987-27908.
Buchholz, Herwig; Surya Prakash, G. K.; Deffieux, Denis; Olah, George (1999). “Electrochemical preparation of tris(tert-butyldimethylsilyl)cyclopropene and its hydride abstraction to tris(tert-butyldimethylsilyl)cyclopropenium tetrafluoroborate”. Proc. Natl. Acad. Sci. 96 (18): 10003–10005. Bibcode:1999PNAS...9610003B. doi:10.1073/pnas.96.18.10003. PMC 17831. PMID 10468551.
Bandar, Jeffrey S.; Lambert, Tristan H. (2013). “Aminocyclopropenium ions: synthesis, properties, and applications”. Synthesis 45 (10): 2485–2498. doi:10.1055/s-0033-1338516.
Haley, Michael M.; Gilbertson, Robert D.; Weakley, Timothy J.D. (2000). “Preparation, X-ray Crystal Structures, and Reactivity of Alkynylcyclopropenylium Salts”. Journal of Organic Chemistry 65 (5): 1422–1430. doi:10.1021/jo9915372. PMID 10814104.
Hardee, David J.; Kovalchuke, Lyudmila; Lambert, Tristan H. (2010). “Nucleophilic Acyl Substitution via Aromatic Cation Activation of Carboxylic Acids: Rapid Generation of Acid Chlorides under Mild Conditions”. Journal of the American Chemical Society 132 (14): 5002–5003. doi:10.1021/ja101292a. PMID 20297823.
Nogueira, J. M.; Nguyến, S. H.; Bennett, C. S. (2011). “Cyclopropenium Cation Promoted Dehydrative Glycosylations Using 2-Deoxy- and 2,6-Dideoxy-Sugar Donors”. Journal of the American Chemical Society 13 (11): 2184–2187. doi:10.1021/ol200726v. PMID 21548642.
Yoshida, Zen'ichi; Yoneda, Shigeo; Hirai, Hideo (1981). “A Novel Synthesis of Pyrroles by the Reactions of Tris(alkylthio)cyclopropenium Salt with Amines”. Heterocycles 15 (2): 865. doi:10.3987/S-1981-02-0865.
Chiang, T.; Kerber, R. C.; Kimball, S. D.; Lauher, J. W. (1979). “(η³-Triphenylcyclopropenyl) Tricarbonylcobalt”. Inorganic Chemistry 18 (6): 1687–1691. doi:10.1021/ic50196a058.
Jiang, Yivan; Freyer, Jessica; Cotanda, Pepa; Brucks, Spencer; Killops, Kato; Bandar, Jeffrey; Torsitano, Christopher; Balsara, Nitash et al. (2015). “The evolution of cyclopropenium ions into functional polyelectrolytes”. Nature Communications 6 (1): 1–7. Bibcode:2015NatCo...6E5950J. doi:10.1038/ncomms6950. PMC 4354017. PMID 25575214.

escholarship.org (Global: 1,477^th place; Japanese: 3,984^th place)

cloudfront.escholarship.org

Jiang, Yivan; Freyer, Jessica; Cotanda, Pepa; Brucks, Spencer; Killops, Kato; Bandar, Jeffrey; Torsitano, Christopher; Balsara, Nitash et al. (2015). “The evolution of cyclopropenium ions into functional polyelectrolytes”. Nature Communications 6 (1): 1–7. Bibcode:2015NatCo...6E5950J. doi:10.1038/ncomms6950. PMC 4354017. PMID 25575214.

nih.gov (Global: 5^th place; Japanese: 11^th place)

pubmed.ncbi.nlm.nih.gov

Buchholz, Herwig; Surya Prakash, G. K.; Deffieux, Denis; Olah, George (1999). “Electrochemical preparation of tris(tert-butyldimethylsilyl)cyclopropene and its hydride abstraction to tris(tert-butyldimethylsilyl)cyclopropenium tetrafluoroborate”. Proc. Natl. Acad. Sci. 96 (18): 10003–10005. Bibcode:1999PNAS...9610003B. doi:10.1073/pnas.96.18.10003. PMC 17831. PMID 10468551.
Haley, Michael M.; Gilbertson, Robert D.; Weakley, Timothy J.D. (2000). “Preparation, X-ray Crystal Structures, and Reactivity of Alkynylcyclopropenylium Salts”. Journal of Organic Chemistry 65 (5): 1422–1430. doi:10.1021/jo9915372. PMID 10814104.
Hardee, David J.; Kovalchuke, Lyudmila; Lambert, Tristan H. (2010). “Nucleophilic Acyl Substitution via Aromatic Cation Activation of Carboxylic Acids: Rapid Generation of Acid Chlorides under Mild Conditions”. Journal of the American Chemical Society 132 (14): 5002–5003. doi:10.1021/ja101292a. PMID 20297823.
Nogueira, J. M.; Nguyến, S. H.; Bennett, C. S. (2011). “Cyclopropenium Cation Promoted Dehydrative Glycosylations Using 2-Deoxy- and 2,6-Dideoxy-Sugar Donors”. Journal of the American Chemical Society 13 (11): 2184–2187. doi:10.1021/ol200726v. PMID 21548642.
Jiang, Yivan; Freyer, Jessica; Cotanda, Pepa; Brucks, Spencer; Killops, Kato; Bandar, Jeffrey; Torsitano, Christopher; Balsara, Nitash et al. (2015). “The evolution of cyclopropenium ions into functional polyelectrolytes”. Nature Communications 6 (1): 1–7. Bibcode:2015NatCo...6E5950J. doi:10.1038/ncomms6950. PMC 4354017. PMID 25575214.

ncbi.nlm.nih.gov

Buchholz, Herwig; Surya Prakash, G. K.; Deffieux, Denis; Olah, George (1999). “Electrochemical preparation of tris(tert-butyldimethylsilyl)cyclopropene and its hydride abstraction to tris(tert-butyldimethylsilyl)cyclopropenium tetrafluoroborate”. Proc. Natl. Acad. Sci. 96 (18): 10003–10005. Bibcode:1999PNAS...9610003B. doi:10.1073/pnas.96.18.10003. PMC 17831. PMID 10468551.
Jiang, Yivan; Freyer, Jessica; Cotanda, Pepa; Brucks, Spencer; Killops, Kato; Bandar, Jeffrey; Torsitano, Christopher; Balsara, Nitash et al. (2015). “The evolution of cyclopropenium ions into functional polyelectrolytes”. Nature Communications 6 (1): 1–7. Bibcode:2015NatCo...6E5950J. doi:10.1038/ncomms6950. PMC 4354017. PMID 25575214.

pnas.org (Global: 1,411^th place; Japanese: 1,422^nd place)

Buchholz, Herwig; Surya Prakash, G. K.; Deffieux, Denis; Olah, George (1999). “Electrochemical preparation of tris(tert-butyldimethylsilyl)cyclopropene and its hydride abstraction to tris(tert-butyldimethylsilyl)cyclopropenium tetrafluoroborate”. Proc. Natl. Acad. Sci. 96 (18): 10003–10005. Bibcode:1999PNAS...9610003B. doi:10.1073/pnas.96.18.10003. PMC 17831. PMID 10468551.

シクロプロペニウム (Japanese Wikipedia)

adsabs.harvard.edu (Global: 14th place; Japanese: 60th place)

ui.adsabs.harvard.edu

books.google.com (Global: 3rd place; Japanese: 40th place)

doi.org (Global: 2nd place; Japanese: 3rd place)

escholarship.org (Global: 1,477th place; Japanese: 3,984th place)