Resorcinol (English Wikipedia)

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

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18doi.org

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7nih.gov

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3books.google.com

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2worldcat.org

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2harvard.edu

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acs.org

cen.acs.org

McCoy, Michael. "Resorcinol plant to close". Chemical & Engineering News. American Chemical Society. Retrieved 6 December 2023.

books.google.com

Wood adhesives, Pizzi & Mittal, 2010
Weselsky, P (1871). "Neue Derivate des Resorcins" [New derivatives of resorcinol]. Berichte der Deutschen Chemischen Gesellschaft. 4: 32–33. doi:10.1002/cber.18710040114.
Piccard, J.; Humbert, A. (1876). "Ueber eine Resorcindisulfosäure" [On a resorcinol disulfonic acid]. Berichte der Deutschen Chemischen Gesellschaft. 9 (2): 1479–1483. doi:10.1002/cber.187600902133.

cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0543". National Institute for Occupational Safety and Health (NIOSH).

chemicalwatch.com

"Resorcinol to be added to REACH candidate list after long battle". Chemical Watch. 10 February 2022. Retrieved 16 August 2022.

doi.org

"Front Matter". Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 691. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
Gawron, O.; Duggan, M.; Grelechi, C. (1952). "Manometric Determination of Dissociation Constants of Phenols". Analytical Chemistry. 24 (6): 969–970. doi:10.1021/ac60066a013.
Lander, John J.; Svirbely, John J. Lander, W. J. (1945). "The Dipole Moments of Catechol, Resorcinol and Hydroquinone". Journal of the American Chemical Society. 67 (2): 322–324. doi:10.1021/ja01218a051.{{cite journal}}: CS1 maint: multiple names: authors list (link)
K. W. Schmiedel; D. Decker (2012). "Resorcinol". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a23_111.pub2. ISBN 978-3527306732.
Meyer, J (1897). "Notiz über die Umwandlung von Aminen in Phenole". Berichte der Deutschen Chemischen Gesellschaft. 30 (3): 2568–2569. doi:10.1002/cber.18970300334.
Thompson, R. B. (1947). "Dihydroresorcinol". Org. Synth. 27: 21. doi:10.15227/orgsyn.027.0021.
Mekler, A. B.; Ramachandran, S.; Swaminathan, S.; Newman, Melvin S. (1961). "Methyl-1,3-Cyclohexanedione". Org. Synth. 41: 56. doi:10.15227/orgsyn.041.0056.
Nencki, M.; Sieber, N. (1881). "Über die Verbindungen der ein- und zweibasischen Fettsäuren mit Phenolen". Journal für Praktische Chemie. 23 (1): 147–156. doi:10.1002/prac.18810230111.
Traub, M. C.; Hock, C. (1884). "Ueber ein Lakmoid". Berichte der Deutschen Chemischen Gesellschaft. 17 (2): 2615–2617. doi:10.1002/cber.188401702192.
Michael, Arthur (1888). "Ueber das Verhalten von Natriummalonäther gegen Resorcinol". Journal für Praktische Chemie. 37 (1): 469–471. doi:10.1002/prac.18880370144.
Cheng, H. A.; Drinnan, C. T.; Pleshko, N.; Fisher, O. Z. (21 October 2015). "Pseudotannins Self-assembled into Antioxidant Complexes". Soft Matter. 11 (39): 7783–7791. Bibcode:2015SMat...11.7783C. doi:10.1039/c5sm01224d. ISSN 1744-683X. PMC 4589535. PMID 26313262.
Suzuki, Y (1999). "Structures of 5-alkylresorcinol-related analogues in rye". Phytochemistry. 52 (2): 281–289. doi:10.1016/S0031-9422(99)00196-X.
Boer, J; Jemec, GB (2010). "Resorcinol peels as a possible self-treatment of painful nodules in hidradenitis suppurativa". Clinical and Experimental Dermatology. 35 (1): 36–40. doi:10.1111/j.1365-2230.2009.03377.x. PMID 19549239. S2CID 1794323.
Weselsky, P (1871). "Neue Derivate des Resorcins" [New derivatives of resorcinol]. Berichte der Deutschen Chemischen Gesellschaft. 4: 32–33. doi:10.1002/cber.18710040114.
Piccard, J.; Humbert, A. (1876). "Ueber eine Resorcindisulfosäure" [On a resorcinol disulfonic acid]. Berichte der Deutschen Chemischen Gesellschaft. 9 (2): 1479–1483. doi:10.1002/cber.187600902133.
Sidera, K.; Patsavoudi, E. (January 2014). "HSP90 inhibitors: current development and potential in cancer therapy". Recent Patents on Anti-Cancer Drug Discovery. 9 (1): 1–20. doi:10.2174/15748928113089990031. PMID 23312026.
Biamonte, M. A.; Van de Water, R.; Arndt, J. W.; Scannevin, R. H.; Perret, D.; Lee, W.-C. (January 2010). "Heat shock protein 90: Inhibitors in clinical trials". Journal of Medicinal Chemistry. 53 (1): 3–17. doi:10.1021/jm9004708. PMID 20055425.
McConnell, Virginia F. (1953). "Hlasiwetz and Barth — Pioneers in the structural aspects of plant products". Journal of Chemical Education. 30 (8): 380. Bibcode:1953JChEd..30..380M. doi:10.1021/ed030p380.

elsevier.com

linkinghub.elsevier.com

Suzuki, Y (1999). "Structures of 5-alkylresorcinol-related analogues in rye". Phytochemistry. 52 (2): 281–289. doi:10.1016/S0031-9422(99)00196-X.

harvard.edu

ui.adsabs.harvard.edu

Cheng, H. A.; Drinnan, C. T.; Pleshko, N.; Fisher, O. Z. (21 October 2015). "Pseudotannins Self-assembled into Antioxidant Complexes". Soft Matter. 11 (39): 7783–7791. Bibcode:2015SMat...11.7783C. doi:10.1039/c5sm01224d. ISSN 1744-683X. PMC 4589535. PMID 26313262.
McConnell, Virginia F. (1953). "Hlasiwetz and Barth — Pioneers in the structural aspects of plant products". Journal of Chemical Education. 30 (8): 380. Bibcode:1953JChEd..30..380M. doi:10.1021/ed030p380.

hathitrust.org

babel.hathitrust.org

H. Hlasiwetz and L. Barth (1864) "Ueber einen neuen, dem Orcin homologen Körper" (On a new substance homologous to orcin), Annalen der Chemie, 130 (3) : 354-359. Resorcinol is named on p. 358: "Wir nennen den neuen Körper, da wir gefunden haben, dass er auch aus dem Ammoniakgummiharz erhalten werden kann, Resorcin, um an seine Entstehung aus Harzen und seine Beziehung zum Orcin zu erinnern." (We name the new substance, since we have found that it can be obtained from ammoniated resin gum, resorcin, in order to recall its creation from resin and its relation to orcin.)

nih.gov

pubmed.ncbi.nlm.nih.gov

Cheng, H. A.; Drinnan, C. T.; Pleshko, N.; Fisher, O. Z. (21 October 2015). "Pseudotannins Self-assembled into Antioxidant Complexes". Soft Matter. 11 (39): 7783–7791. Bibcode:2015SMat...11.7783C. doi:10.1039/c5sm01224d. ISSN 1744-683X. PMC 4589535. PMID 26313262.
Boer, J; Jemec, GB (2010). "Resorcinol peels as a possible self-treatment of painful nodules in hidradenitis suppurativa". Clinical and Experimental Dermatology. 35 (1): 36–40. doi:10.1111/j.1365-2230.2009.03377.x. PMID 19549239. S2CID 1794323.
Wipperman, J; Bragg, DA; Litzner, B (1 November 2019). "Hidradenitis Suppurativa: Rapid Evidence Review". American Family Physician. 100 (9): 562–569. PMID 31674740.
Sidera, K.; Patsavoudi, E. (January 2014). "HSP90 inhibitors: current development and potential in cancer therapy". Recent Patents on Anti-Cancer Drug Discovery. 9 (1): 1–20. doi:10.2174/15748928113089990031. PMID 23312026.
Biamonte, M. A.; Van de Water, R.; Arndt, J. W.; Scannevin, R. H.; Perret, D.; Lee, W.-C. (January 2010). "Heat shock protein 90: Inhibitors in clinical trials". Journal of Medicinal Chemistry. 53 (1): 3–17. doi:10.1021/jm9004708. PMID 20055425.

ncbi.nlm.nih.gov

Cheng, H. A.; Drinnan, C. T.; Pleshko, N.; Fisher, O. Z. (21 October 2015). "Pseudotannins Self-assembled into Antioxidant Complexes". Soft Matter. 11 (39): 7783–7791. Bibcode:2015SMat...11.7783C. doi:10.1039/c5sm01224d. ISSN 1744-683X. PMC 4589535. PMID 26313262.

pubchem.ncbi.nlm.nih.gov

Euresol, PubChem

semanticscholar.org

api.semanticscholar.org

Boer, J; Jemec, GB (2010). "Resorcinol peels as a possible self-treatment of painful nodules in hidradenitis suppurativa". Clinical and Experimental Dermatology. 35 (1): 36–40. doi:10.1111/j.1365-2230.2009.03377.x. PMID 19549239. S2CID 1794323.

worldcat.org

search.worldcat.org

CRC handbook of chemistry and physics: a ready-reference book of chemical and physical data. William M. Haynes, David R. Lide, Thomas J. Bruno (2016-2017, 97th ed.). Boca Raton, Florida. 2016. ISBN 978-1-4987-5428-6. OCLC 930681942.{{cite book}}: CS1 maint: location missing publisher (link) CS1 maint: others (link)
Cheng, H. A.; Drinnan, C. T.; Pleshko, N.; Fisher, O. Z. (21 October 2015). "Pseudotannins Self-assembled into Antioxidant Complexes". Soft Matter. 11 (39): 7783–7791. Bibcode:2015SMat...11.7783C. doi:10.1039/c5sm01224d. ISSN 1744-683X. PMC 4589535. PMID 26313262.

zenodo.org

Meyer, J (1897). "Notiz über die Umwandlung von Aminen in Phenole". Berichte der Deutschen Chemischen Gesellschaft. 30 (3): 2568–2569. doi:10.1002/cber.18970300334.
Nencki, M.; Sieber, N. (1881). "Über die Verbindungen der ein- und zweibasischen Fettsäuren mit Phenolen". Journal für Praktische Chemie. 23 (1): 147–156. doi:10.1002/prac.18810230111.
Traub, M. C.; Hock, C. (1884). "Ueber ein Lakmoid". Berichte der Deutschen Chemischen Gesellschaft. 17 (2): 2615–2617. doi:10.1002/cber.188401702192.
Michael, Arthur (1888). "Ueber das Verhalten von Natriummalonäther gegen Resorcinol". Journal für Praktische Chemie. 37 (1): 469–471. doi:10.1002/prac.18880370144.