Thiophenol (English Wikipedia)

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

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7doi.org

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4orgsyn.org

2,971^st place

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2cdc.gov

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2semanticscholar.org

11^th place

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1espacenet.com

800^th place

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1nih.gov

4^th place

1handle.net

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cdc.gov

NIOSH Pocket Guide to Chemical Hazards. "#0050". National Institute for Occupational Safety and Health (NIOSH).
CDC - NIOSH Pocket Guide to Chemical Hazards

doi.org

"Front Matter". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. P001–P004. doi:10.1039/9781849733069-FP001 (inactive 2024-06-30). ISBN 978-0-85404-182-4.{{cite book}}: CS1 maint: DOI inactive as of June 2024 (link)
Bordwell, Frederick G.; Hughes, David L. (1982). "Thiol acidities and thiolate ion reactivities toward butyl chloride in dimethyl sulfoxide solution. The question of curvature in Broensted plots". The Journal of Organic Chemistry. 47 (17): 3224–3232. doi:10.1021/jo00138a005.
Melvin S. Newman and Frederick W. Hetzel (1971). "Thiophenols from Phenols: 2-Naphthalenethiol". Organic Syntheses. 51: 139. doi:10.15227/orgsyn.051.0139.
Tarbell, D. S.; Fukushima, D. K. (1947). "m-Thiocresol". Organic Syntheses. 27: 81. doi:10.15227/orgsyn.027.0081; Collected Volumes, vol. 3, p. 809.
Kazem-Rostami, Masoud; Khazaei, Ardeshir; Moosavi-Zare, Ahmad; Bayat, Mohammad; Saednia, Shahnaz (2012). "One-pot synthesis of thiophenols". Synlett. 23 (13): 1893–1896. doi:10.1055/s-0032-1316557. S2CID 196805424.
Jiang, Y.; Qin, Y.; Xie, S.; Zhang, X.; Dong, J.; Ma, D., A (2009). "General and Efficient Approach to Aryl Thiols: CuI-Catalyzed Coupling of Aryl Iodides with Sulfur and Subsequent Reduction". Organic Letters. 22 (1): 52–56. doi:10.1021/acs.orglett.9b03866. PMID 31833778. S2CID 209341111.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Campopiano, O. (2004). "Thiophenol". Encyclopedia of Reagents for Organic Synthesis. New York: John Wiley & Sons. doi:10.1002/047084289X. hdl:10261/236866. ISBN 9780471936237..

espacenet.com

worldwide.espacenet.com

US Patent 2,490,257, Duncan J. Crowley & Alvin L Kosak, "Mono- and Polyalkyl Mono- and Polynuclear Mercaptans", issued 1949-12-06, assigned to Socony-Vacuum Oil Co.

handle.net

hdl.handle.net

Campopiano, O. (2004). "Thiophenol". Encyclopedia of Reagents for Organic Synthesis. New York: John Wiley & Sons. doi:10.1002/047084289X. hdl:10261/236866. ISBN 9780471936237..

nih.gov

pubmed.ncbi.nlm.nih.gov

Jiang, Y.; Qin, Y.; Xie, S.; Zhang, X.; Dong, J.; Ma, D., A (2009). "General and Efficient Approach to Aryl Thiols: CuI-Catalyzed Coupling of Aryl Iodides with Sulfur and Subsequent Reduction". Organic Letters. 22 (1): 52–56. doi:10.1021/acs.orglett.9b03866. PMID 31833778. S2CID 209341111.{{cite journal}}: CS1 maint: multiple names: authors list (link)

orgsyn.org

Adams, R.; C. S. Marvel, C. S. "Thiophenol". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 1, p. 504..
Tarbell, D. S.; Fukushima, D. K. (1947). "m-Thiocresol". Organic Syntheses. 27: 81. doi:10.15227/orgsyn.027.0081; Collected Volumes, vol. 3, p. 809.
Barrett, A. G. M.; Dhanak, D.; Graboski, G. G.; Taylor, S. J. (1993). "(Phenylthio)nitromethane". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 8, p. 550.
Posner, G. H.; Whitten, C. E. "Secondary and Tertiary Alkyl Ketones from Carboxylic Acid Chlorides and Lithium Phenylthio(alkyl)cuprate Reagents: tert-Butyl Phenyl Ketone". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 6, p. 248.

semanticscholar.org

api.semanticscholar.org

Kazem-Rostami, Masoud; Khazaei, Ardeshir; Moosavi-Zare, Ahmad; Bayat, Mohammad; Saednia, Shahnaz (2012). "One-pot synthesis of thiophenols". Synlett. 23 (13): 1893–1896. doi:10.1055/s-0032-1316557. S2CID 196805424.
Jiang, Y.; Qin, Y.; Xie, S.; Zhang, X.; Dong, J.; Ma, D., A (2009). "General and Efficient Approach to Aryl Thiols: CuI-Catalyzed Coupling of Aryl Iodides with Sulfur and Subsequent Reduction". Organic Letters. 22 (1): 52–56. doi:10.1021/acs.orglett.9b03866. PMID 31833778. S2CID 209341111.{{cite journal}}: CS1 maint: multiple names: authors list (link)