Imidazol (Swedish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Imidazol" in Swedish language version.

refsWebsite

Global rank Swedish rank

10doi.org

2^nd place

14^th place

5nih.gov

4^th place

17^th place

3harvard.edu

18^th place

162^nd place

2hathitrust.org

441^st place

4,566^th place

2worldcat.org

5^th place

9^th place

1csic.es

2,323^rd place

3,958^th place

1books.google.com

3^rd place

37^th place

1nist.gov

355^th place

299^th place

1sigmaaldrich.com

924^th place

low place

books.google.com

Davis, Jennifer L.; Papich, Mark G.; Heit, Mark C. (2009). ”Chapter 39: Antifungal and Antiviral Drugs”. i Riviere, Jim E.; Papich, Mark G.. Veterinary Pharmacology and Therapeutics (9th). Wiley-Blackwell. Sid. 1019–1020. ISBN 978-0-8138-2061-3.

csic.es

digital.csic.es

Castaño, T.; Encinas, A.; Pérez, C.; Castro, A.; Campillo, N. E.; Gil, C. (2008). ”Design, synthesis, and evaluation of potential inhibitors of nitric oxide synthase”. Bioorg. Med. Chem. 16 (11): sid. 6193–6206. doi:10.1016/j.bmc.2008.04.036. PMID 18477512. https://digital.csic.es/bitstream/10261/87090/1/accesoRestringido.pdf.

doi.org

dx.doi.org

Rosemeyer, H. (2004). ”The Chemodiversity of Purine as a Constituent of Natural Products”. Chemistry & Biodiversity 1 (3): sid. 361–401. doi:10.1002/cbdv.200490033. PMID 17191854.
Christen, Dines; Griffiths, John H.; Sheridan, John (1981). ”The Microwave Spectrum of Imidazole; Complete Structure and the Electron Distribution from Nuclear Quadrupole Coupling Tensors and Dipole Moment Orientation”. Zeitschrift für Naturforschung A 36 (12): sid. 1378–1385. doi:10.1515/zna-1981-1220. Bibcode: 1981ZNatA..36.1378C.
Debus, Heinrich (1858). ”Ueber die Einwirkung des Ammoniaks auf Glyoxal”. Annalen der Chemie und Pharmacie 107 (2): sid. 199–208. doi:10.1002/jlac.18581070209. https://babel.hathitrust.org/cgi/pt?id=njp.32101044011045;view=1up;seq=211. From p. 205: "Die gereinigte Substanz stellt das oxalsaure Salz einer Basis dar, die ich mit Glyoxalin bezeichenen werde." (The purified substance constitutes the oxalic salt of a base, which I will designate as "glyoxaline".)
Crouch, R. David; Howard, Jessica L.; Zile, Jennifer L.; Barker, Kathryn H. (2006). ”Microwave-Mediated Synthesis of Lophine: Developing a Mechanism To Explain a Product”. J. Chem. Educ. 83 (11): sid. 1658. doi:10.1021/ed083p1658. Bibcode: 2006JChEd..83.1658C.
Van Leusen, Albert M.; Wildeman, Jurjen; Oldenziel, Otto H. (1977). ”Chemistry of sulfonylmethyl isocyanides. 12. Base-induced cycloaddition of sulfonylmethyl isocyanides to carbon, nitrogen double bonds. Synthesis of 1,5-disubstituted and 1,4,5-trisubstituted imidazoles from aldimines and imidoyl chlorides”. Journal of Organic Chemistry 42 (7): sid. 1153–1159. doi:10.1021/jo00427a012. Bibcode: 1977JOrgC..42.1153A.
Castaño, T.; Encinas, A.; Pérez, C.; Castro, A.; Campillo, N. E.; Gil, C. (2008). ”Design, synthesis, and evaluation of potential inhibitors of nitric oxide synthase”. Bioorg. Med. Chem. 16 (11): sid. 6193–6206. doi:10.1016/j.bmc.2008.04.036. PMID 18477512. https://digital.csic.es/bitstream/10261/87090/1/accesoRestringido.pdf.
Bogle, R. G.; Whitley, G. S.; Soo, S. C.; Johnstone, A. P.; Vallance, P. (1994). ”Effect of anti-fungal imidazoles on mRNA levels and enzyme activity of inducible nitric oxide synthase”. Br. J. Pharmacol. 111 (4): sid. 1257–1261. doi:10.1111/j.1476-5381.1994.tb14881.x. PMID 7518297.
Khalid, M. H.; Tokunaga, Y.; Caputy, A. J.; Walters, E. (2005). ”Inhibition of tumor growth and prolonged survival of rats with intracranial gliomas following administration of clotrimazole”. J. Neurosurg. 103 (1): sid. 79–86. doi:10.3171/jns.2005.103.1.0079. PMID 16121977.
Sunderland, M. R.; Cruickshank, R. H.; Leighs, S. J. (2014). ”The efficacy of antifungal azole and antiprotozoal compounds in protection of wool from keratin-digesting insect larvae”. Textile Res. J. 84 (9): sid. 924–931. doi:10.1177/0040517513515312.
Molina, F; Rueda, A; Bosque-Sendra, J.M; Megias, L (1996). ”Determination of proteins in the presence of imidazole buffers”. Journal of Pharmaceutical and Biomedical Analysis (Elsevier BV) 14 (3): sid. 273–280. doi:10.1016/0731-7085(95)01615-5. ISSN 0731-7085. PMID 8851751.

harvard.edu

adsabs.harvard.edu

Christen, Dines; Griffiths, John H.; Sheridan, John (1981). ”The Microwave Spectrum of Imidazole; Complete Structure and the Electron Distribution from Nuclear Quadrupole Coupling Tensors and Dipole Moment Orientation”. Zeitschrift für Naturforschung A 36 (12): sid. 1378–1385. doi:10.1515/zna-1981-1220. Bibcode: 1981ZNatA..36.1378C.
Crouch, R. David; Howard, Jessica L.; Zile, Jennifer L.; Barker, Kathryn H. (2006). ”Microwave-Mediated Synthesis of Lophine: Developing a Mechanism To Explain a Product”. J. Chem. Educ. 83 (11): sid. 1658. doi:10.1021/ed083p1658. Bibcode: 2006JChEd..83.1658C.
Van Leusen, Albert M.; Wildeman, Jurjen; Oldenziel, Otto H. (1977). ”Chemistry of sulfonylmethyl isocyanides. 12. Base-induced cycloaddition of sulfonylmethyl isocyanides to carbon, nitrogen double bonds. Synthesis of 1,5-disubstituted and 1,4,5-trisubstituted imidazoles from aldimines and imidoyl chlorides”. Journal of Organic Chemistry 42 (7): sid. 1153–1159. doi:10.1021/jo00427a012. Bibcode: 1977JOrgC..42.1153A.

hathitrust.org

babel.hathitrust.org

Hantzsch, A. and Weber, J. H. (1887) "Ueber Verbindungen des Thiazols (Pyridins der Thiophenreihe)" (On compounds of thiazole (pyridines of the thiophene series), Berichte der deutschen chemischen Gesellschaft, 20 : 3118–3132, see p. 3119. See also: Hantzsch, A. (1888) "Allegemeine Bemerkungen über Azole" (General observations about azoles), Annalen der Chemie, 249 : 1–6. Hantzsch proposed a reform of the nomenclature of azole compounds, including a proposal to call the heterocyclic ring C₃H₃(NH)N "imidazole" ; see pp. 2 and 4.
Debus, Heinrich (1858). ”Ueber die Einwirkung des Ammoniaks auf Glyoxal”. Annalen der Chemie und Pharmacie 107 (2): sid. 199–208. doi:10.1002/jlac.18581070209. https://babel.hathitrust.org/cgi/pt?id=njp.32101044011045;view=1up;seq=211. From p. 205: "Die gereinigte Substanz stellt das oxalsaure Salz einer Basis dar, die ich mit Glyoxalin bezeichenen werde." (The purified substance constitutes the oxalic salt of a base, which I will designate as "glyoxaline".)

nih.gov

ncbi.nlm.nih.gov

Rosemeyer, H. (2004). ”The Chemodiversity of Purine as a Constituent of Natural Products”. Chemistry & Biodiversity 1 (3): sid. 361–401. doi:10.1002/cbdv.200490033. PMID 17191854.
Castaño, T.; Encinas, A.; Pérez, C.; Castro, A.; Campillo, N. E.; Gil, C. (2008). ”Design, synthesis, and evaluation of potential inhibitors of nitric oxide synthase”. Bioorg. Med. Chem. 16 (11): sid. 6193–6206. doi:10.1016/j.bmc.2008.04.036. PMID 18477512. https://digital.csic.es/bitstream/10261/87090/1/accesoRestringido.pdf.
Bogle, R. G.; Whitley, G. S.; Soo, S. C.; Johnstone, A. P.; Vallance, P. (1994). ”Effect of anti-fungal imidazoles on mRNA levels and enzyme activity of inducible nitric oxide synthase”. Br. J. Pharmacol. 111 (4): sid. 1257–1261. doi:10.1111/j.1476-5381.1994.tb14881.x. PMID 7518297.
Khalid, M. H.; Tokunaga, Y.; Caputy, A. J.; Walters, E. (2005). ”Inhibition of tumor growth and prolonged survival of rats with intracranial gliomas following administration of clotrimazole”. J. Neurosurg. 103 (1): sid. 79–86. doi:10.3171/jns.2005.103.1.0079. PMID 16121977.
Molina, F; Rueda, A; Bosque-Sendra, J.M; Megias, L (1996). ”Determination of proteins in the presence of imidazole buffers”. Journal of Pharmaceutical and Biomedical Analysis (Elsevier BV) 14 (3): sid. 273–280. doi:10.1016/0731-7085(95)01615-5. ISSN 0731-7085. PMID 8851751.

nist.gov

webbook.nist.gov

”1H-Imidazole”. https://webbook.nist.gov/cgi/cbook.cgi?ID=C288324&Mask=400. Läst 13 maj 2021.

sigmaaldrich.com

”Optimizing Purification of Histidine-Tagged Proteins”. https://www.sigmaaldrich.com/technical-documents/protocols/biology/affinity-chromatography-tagged-proteins/optimizing-purification-of-histidine-tagged-proteins.html. Läst 13 maj 2021.

worldcat.org

Dawson, R. M. C. (1986). Data for biochemical research. Oxford: Clarendon Press. Sid. 325. ISBN 978-0-19-855299-4. OCLC 11865673.
Molina, F; Rueda, A; Bosque-Sendra, J.M; Megias, L (1996). ”Determination of proteins in the presence of imidazole buffers”. Journal of Pharmaceutical and Biomedical Analysis (Elsevier BV) 14 (3): sid. 273–280. doi:10.1016/0731-7085(95)01615-5. ISSN 0731-7085. PMID 8851751.