Phenols (English Wikipedia)

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

refsWebsite

Global rank English rank

13doi.org

2^nd place

6nih.gov

4^th place

3zenodo.org

621^st place

380^th place

2bnf.fr

124^th place

544^th place

2semanticscholar.org

11^th place

8^th place

1iupac.org

538^th place

863^rd place

1orgsynth.org

low place

1harvard.edu

18^th place

17^th place

1books.google.com

3^rd place

1acs.org

1,248^th place

1,104^th place

1worldcat.org

5^th place

acs.org

pubs.acs.org

Scott, Kevin A.; Cox, Philip B.; Njardarson, Jon T. (2022-05-26). "Phenols in Pharmaceuticals: Analysis of a Recurring Motif". Journal of Medicinal Chemistry. 65 (10): 7044–7072. doi:10.1021/acs.jmedchem.2c00223. ISSN 0022-2623. PMID 35533692. S2CID 248667453.

bnf.fr

gallica.bnf.fr

Bamberger, E. (1894). "Ueber die Reduction der Nitroverbindungen". Chemische Berichte. 27 (2): 1347–1350. doi:10.1002/cber.18940270229.
Bamberger, E. (1894). "Über das Phenylhydroxylamin". Chemische Berichte. 27 (2): 1548–1557. doi:10.1002/cber.18940270276.

books.google.com

Wilfred Vermerris and Ralph Nicholson. Phenolic Compound Biochemistry Springer, 2008.

doi.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "phenols". doi:10.1351/goldbook.P04539
Hättenschwiler, Stephan; Vitousek, Peter M. (2000). "The role of polyphenols in terrestrial ecosystem nutrient cycling". Trends in Ecology & Evolution. 15 (6): 238–243. doi:10.1016/S0169-5347(00)01861-9. PMID 10802549.
Fiege H; Voges H-W; Hamamoto T; Umemura S; Iwata T; Miki H; Fujita Y; Buysch H-J; Garbe D; Paulus W (2000). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313. ISBN 978-3527306732. {{cite encyclopedia}}: |work= ignored (help)
Carreño, M. Carmen; González-López, Marcos; Urbano, Antonio (2006). "Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet Oxygen". Angewandte Chemie International Edition. 45 (17): 2737–2741. doi:10.1002/anie.200504605. PMID 16548026.
Fries, K.; Finck, G. (1908). "Über Homologe des Cumaranons und ihre Abkömmlinge". Chemische Berichte. 41 (3): 4271–4284. doi:10.1002/cber.190804103146.
Fries, K.; Pfaffendorf, W. (1910). "Über ein Kondensationsprodukt des Cumaranons und seine Umwandlung in Oxindirubin". Chemische Berichte. 43 (1): 212–219. doi:10.1002/cber.19100430131.
Bamberger, E. (1894). "Ueber die Reduction der Nitroverbindungen". Chemische Berichte. 27 (2): 1347–1350. doi:10.1002/cber.18940270229.
Bamberger, E. (1894). "Über das Phenylhydroxylamin". Chemische Berichte. 27 (2): 1548–1557. doi:10.1002/cber.18940270276.
H. Bucherer (1904). "Über die Einwirkung schwefligsaurer Salze auf aromatische Amido- und Hydroxylverbindungen". J. Prakt. Chem. (in German). 69 (1): 49–91. doi:10.1002/prac.19040690105.
H. E. Ungnade, E. F. Orwoll (1943). "3-Bromo-4-hydroxytoluene". Organic Syntheses. 23: 11. doi:10.15227/orgsyn.023.0011.
Bracegirdle, Sonia; Anderson, Edward A. (2010). "Arylsilane oxidation—new routes to hydroxylated aromatics". Chem. Comm. 46 (20): 3454–6. doi:10.1039/b924135c. PMID 20582346. S2CID 31736757.
Le Valliant, Franck; Mateos Calbet, Ana; González-Pelayo, Silvia; Reijerse, Edward J.; Ni, Shengyang; Busch, Julia; Cornella, Josep (2022). "Catalytic synthesis of phenols with nitrous oxide". Nature. 604 (7907): 677–683. Bibcode:2022Natur.604..677L. doi:10.1038/s41586-022-04516-4. PMC 9046086. PMID 35478236.
Scott, Kevin A.; Cox, Philip B.; Njardarson, Jon T. (2022-05-26). "Phenols in Pharmaceuticals: Analysis of a Recurring Motif". Journal of Medicinal Chemistry. 65 (10): 7044–7072. doi:10.1021/acs.jmedchem.2c00223. ISSN 0022-2623. PMID 35533692. S2CID 248667453.

harvard.edu

ui.adsabs.harvard.edu

Le Valliant, Franck; Mateos Calbet, Ana; González-Pelayo, Silvia; Reijerse, Edward J.; Ni, Shengyang; Busch, Julia; Cornella, Josep (2022). "Catalytic synthesis of phenols with nitrous oxide". Nature. 604 (7907): 677–683. Bibcode:2022Natur.604..677L. doi:10.1038/s41586-022-04516-4. PMC 9046086. PMID 35478236.

iupac.org

goldbook.iupac.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "phenols". doi:10.1351/goldbook.P04539

nih.gov

pubmed.ncbi.nlm.nih.gov

Hättenschwiler, Stephan; Vitousek, Peter M. (2000). "The role of polyphenols in terrestrial ecosystem nutrient cycling". Trends in Ecology & Evolution. 15 (6): 238–243. doi:10.1016/S0169-5347(00)01861-9. PMID 10802549.
Carreño, M. Carmen; González-López, Marcos; Urbano, Antonio (2006). "Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet Oxygen". Angewandte Chemie International Edition. 45 (17): 2737–2741. doi:10.1002/anie.200504605. PMID 16548026.
Bracegirdle, Sonia; Anderson, Edward A. (2010). "Arylsilane oxidation—new routes to hydroxylated aromatics". Chem. Comm. 46 (20): 3454–6. doi:10.1039/b924135c. PMID 20582346. S2CID 31736757.
Le Valliant, Franck; Mateos Calbet, Ana; González-Pelayo, Silvia; Reijerse, Edward J.; Ni, Shengyang; Busch, Julia; Cornella, Josep (2022). "Catalytic synthesis of phenols with nitrous oxide". Nature. 604 (7907): 677–683. Bibcode:2022Natur.604..677L. doi:10.1038/s41586-022-04516-4. PMC 9046086. PMID 35478236.
Scott, Kevin A.; Cox, Philip B.; Njardarson, Jon T. (2022-05-26). "Phenols in Pharmaceuticals: Analysis of a Recurring Motif". Journal of Medicinal Chemistry. 65 (10): 7044–7072. doi:10.1021/acs.jmedchem.2c00223. ISSN 0022-2623. PMID 35533692. S2CID 248667453.

ncbi.nlm.nih.gov

Le Valliant, Franck; Mateos Calbet, Ana; González-Pelayo, Silvia; Reijerse, Edward J.; Ni, Shengyang; Busch, Julia; Cornella, Josep (2022). "Catalytic synthesis of phenols with nitrous oxide". Nature. 604 (7907): 677–683. Bibcode:2022Natur.604..677L. doi:10.1038/s41586-022-04516-4. PMC 9046086. PMID 35478236.

orgsynth.org

2,4-Hexadienedioic acid, monomethyl ester, (Z,Z)- Organic Syntheses, Coll. Vol. 8, p. 490 (1993); Vol. 66, p. 180 (1988) Article.

semanticscholar.org

api.semanticscholar.org

Bracegirdle, Sonia; Anderson, Edward A. (2010). "Arylsilane oxidation—new routes to hydroxylated aromatics". Chem. Comm. 46 (20): 3454–6. doi:10.1039/b924135c. PMID 20582346. S2CID 31736757.
Scott, Kevin A.; Cox, Philip B.; Njardarson, Jon T. (2022-05-26). "Phenols in Pharmaceuticals: Analysis of a Recurring Motif". Journal of Medicinal Chemistry. 65 (10): 7044–7072. doi:10.1021/acs.jmedchem.2c00223. ISSN 0022-2623. PMID 35533692. S2CID 248667453.

worldcat.org

Scott, Kevin A.; Cox, Philip B.; Njardarson, Jon T. (2022-05-26). "Phenols in Pharmaceuticals: Analysis of a Recurring Motif". Journal of Medicinal Chemistry. 65 (10): 7044–7072. doi:10.1021/acs.jmedchem.2c00223. ISSN 0022-2623. PMID 35533692. S2CID 248667453.

zenodo.org

Fries, K.; Finck, G. (1908). "Über Homologe des Cumaranons und ihre Abkömmlinge". Chemische Berichte. 41 (3): 4271–4284. doi:10.1002/cber.190804103146.
Fries, K.; Pfaffendorf, W. (1910). "Über ein Kondensationsprodukt des Cumaranons und seine Umwandlung in Oxindirubin". Chemische Berichte. 43 (1): 212–219. doi:10.1002/cber.19100430131.
H. Bucherer (1904). "Über die Einwirkung schwefligsaurer Salze auf aromatische Amido- und Hydroxylverbindungen". J. Prakt. Chem. (in German). 69 (1): 49–91. doi:10.1002/prac.19040690105.