Fenol (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fenol" in Serbian language version.

refsWebsite

Global rank Serbian rank

9doi.org

2^nd place

4^th place

3nih.gov

4^th place

8^th place

2cdc.gov

218^th place

138^th place

2books.google.com

3^rd place

2^nd place

2web.archive.org

1^st place

2orgsyn.org

2,971^st place

2,328^th place

2wikipedia.org

low place

1wiley.com

222^nd place

155^th place

1sciencedirect.com

149^th place

283^rd place

1sigmaaldrich.com

924^th place

1,411^th place

1acs.org

1,248^th place

389^th place

1chemguide.co.uk

9,416^th place

3,356^th place

1harvard.edu

18^th place

28^th place

1handle.net

102^nd place

266^th place

1organic-chemistry.org

low place

483^rd place

acs.org

pubs.acs.org

McMurry John E. (1992). Fundamentals of Organic Chemistry (3rd изд.). Belmont: Wadsworth. ISBN 0-534-16218-5.

books.google.com

Smith, Michael B.; March, Jerry (2007). Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th изд.). New York: Wiley-Interscience. ISBN 0-471-72091-7.
Roscoe, Henry (1891). A treatise on chemistry, Volume 3, Part 3. London: Macmillan & Co. стр. 23.

cdc.gov

NIOSH Džepni vodič hemijskih hazarda 0493
„Phenol”. Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).

chemguide.co.uk

„The Acidity of Phenol”. ChemGuide. Jim Clark. Приступљено 5. 8. 2007.

doi.org

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Evan E. Bolton; Yanli Wang; Paul A. Thiessen; Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry. 4: 217—241. doi:10.1016/S1574-1400(08)00012-1.
Kütt, Agnes; Movchun, Valeria; Rodima, Toomas; Dansauer, Timo; Rusanov, Eduard B.; Leito, Ivo; Kaljurand, Ivari; Koppel, Juta; Pihl, Viljar; Koppel, Ivar; Ovsjannikov, Gea; Toom, Lauri; Mishima, Masaaki; Medebielle, Maurice; Lork, Enno; Röschenthaler, Gerd-Volker; Koppel, Ilmar A.; Kolomeitsev, Alexander A. (2008). „Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity of Pentakis(trifluoromethyl)benzene, -toluene, -phenol, and -aniline”. The Journal of Organic Chemistry. 73 (7): 2607—2620. PMID 18324831. doi:10.1021/jo702513w.
Manfred Weber, Markus Weber, Michael Kleine-Boymann "Phenol" in Ullmann's Encyclopedia of Industrial Chemistry 2004, Wiley-VCH. . doi:10.1002/14356007.a19_299.pub2. Недостаје или је празан параметар |title= (помоћ).
Silva, Pedro J. (2009). „Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens.”. J. Org. Chem. 74 (2): 914—916. PMID 19053615. doi:10.1021/jo8018736. hdl:10284/3294.
David Y. Curtin and Allan R. Stein (1966). „2,6,6-Trimethyl-2,4-Cyclohexadione.”. Organic Syntheses. 46: 115. doi:10.15227/orgsyn.046.0115. Архивирано из оригинала 05. 06. 2011. г. Приступљено 20. 07. 2011.
Capponi, Marco; Gut, Ivo G.; Hellrung, Bruno; Persy, Gaby; Wirz, Jakob (1999). „Ketonization equilibria of phenol in aqueous solution”. Can. J. Chem. 77 (5–6): 605—613. doi:10.1139/cjc-77-5-6-605.
Curtin, David Y.; Stein, Allan R. (1966). „2,6,6-Trimethyl-2,4-Cyclohexadione”. Organic Syntheses. 46: 115. doi:10.15227/orgsyn.046.0115. Архивирано из оригинала 05. 06. 2011. г. Приступљено 20. 07. 2011. Непознати параметар |name-list-style= игнорисан (помоћ)

handle.net

hdl.handle.net

Silva, Pedro J. (2009). „Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens.”. J. Org. Chem. 74 (2): 914—916. PMID 19053615. doi:10.1021/jo8018736. hdl:10284/3294.

harvard.edu

isites.harvard.edu

„David A. Evans's explanation” (PDF).

nih.gov

ncbi.nlm.nih.gov

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
Kütt, Agnes; Movchun, Valeria; Rodima, Toomas; Dansauer, Timo; Rusanov, Eduard B.; Leito, Ivo; Kaljurand, Ivari; Koppel, Juta; Pihl, Viljar; Koppel, Ivar; Ovsjannikov, Gea; Toom, Lauri; Mishima, Masaaki; Medebielle, Maurice; Lork, Enno; Röschenthaler, Gerd-Volker; Koppel, Ilmar A.; Kolomeitsev, Alexander A. (2008). „Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity of Pentakis(trifluoromethyl)benzene, -toluene, -phenol, and -aniline”. The Journal of Organic Chemistry. 73 (7): 2607—2620. PMID 18324831. doi:10.1021/jo702513w.
Silva, Pedro J. (2009). „Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens.”. J. Org. Chem. 74 (2): 914—916. PMID 19053615. doi:10.1021/jo8018736. hdl:10284/3294.

organic-chemistry.org

Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (I изд.). Oxford University Press. стр. 531. ISBN 978-0-19-850346-0.

orgsyn.org

David Y. Curtin and Allan R. Stein (1966). „2,6,6-Trimethyl-2,4-Cyclohexadione.”. Organic Syntheses. 46: 115. doi:10.15227/orgsyn.046.0115. Архивирано из оригинала 05. 06. 2011. г. Приступљено 20. 07. 2011.
Curtin, David Y.; Stein, Allan R. (1966). „2,6,6-Trimethyl-2,4-Cyclohexadione”. Organic Syntheses. 46: 115. doi:10.15227/orgsyn.046.0115. Архивирано из оригинала 05. 06. 2011. г. Приступљено 20. 07. 2011. Непознати параметар |name-list-style= игнорисан (помоћ)

sciencedirect.com

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

sigmaaldrich.com

Sigma-Aldrich Co. Retrieved on 24. 03. 2022.

web.archive.org

David Y. Curtin and Allan R. Stein (1966). „2,6,6-Trimethyl-2,4-Cyclohexadione.”. Organic Syntheses. 46: 115. doi:10.15227/orgsyn.046.0115. Архивирано из оригинала 05. 06. 2011. г. Приступљено 20. 07. 2011.
Curtin, David Y.; Stein, Allan R. (1966). „2,6,6-Trimethyl-2,4-Cyclohexadione”. Organic Syntheses. 46: 115. doi:10.15227/orgsyn.046.0115. Архивирано из оригинала 05. 06. 2011. г. Приступљено 20. 07. 2011. Непознати параметар |name-list-style= игнорисан (помоћ)

wikipedia.org

sr.wikipedia.org

Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today. 15 (23-24): 1052—7. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

en.wikipedia.org

Silva, Pedro J. (2009). „Inductive and Resonance Effects on the Acidities of Phenol, Enols, and Carbonyl α-Hydrogens.”. J. Org. Chem. 74 (2): 914—916. PMID 19053615. doi:10.1021/jo8018736. hdl:10284/3294.

wiley.com

onlinelibrary.wiley.com

Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.