Alcohol (chemistry) (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alcohol (chemistry)" in English language version.

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  • "alcohols". IUPAC Gold Book. 2014. doi:10.1351/goldbook.A00204. Retrieved 16 December 2013.
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Alcohols". doi:10.1351/goldbook.A00204
  • Saul Patai, ed. (1971). The Hydroxyl Group. PATAI'S Chemistry of Functional Groups. doi:10.1002/9780470771259. ISBN 978-0-470-77125-9.
  • Armstrong HE (8 July 1892). "Contributions to an international system of nomenclature. The nomenclature of cycloids". Proc. Chem. Soc. 8 (114): 128. doi:10.1039/PL8920800127. As ol is indicative of an OH derivative, there seems no reason why the simple word acid should not connote carboxyl, and why al should not connote COH; the names ethanol ethanal and ethanoic acid or simply ethane acid would then stand for the OH, COH and COOH derivatives of ethane.
  • Falbe J, Bahrmann H, Lipps W, Mayer D. "Alcohols, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_279. ISBN 978-3527306732..
  • Schep LJ, Slaughter RJ, Vale JA, Beasley DM (30 September 2009). "A seaman with blindness and confusion". BMJ. 339: b3929. doi:10.1136/bmj.b3929. PMID 19793790. S2CID 6367081.
  • Zimmerman HE, Burkhart KK, Donovan JW (1999). "Ethylene glycol and methanol poisoning: diagnosis and treatment". Journal of Emergency Nursing. 25 (2): 116–20. doi:10.1016/S0099-1767(99)70156-X. PMID 10097201.
  • Lobert S (2000). "Ethanol, isopropanol, methanol, and ethylene glycol poisoning". Critical Care Nurse. 20 (6): 41–7. doi:10.4037/ccn2000.20.6.41. PMID 11878258.
  • Nimz HH, Schmitt U, Schwab E, Wittmann O, Wolf F (2000). "Wood". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a28_305. ISBN 978-3-527-30385-4.
  • Lichtenthaler FW (2010). "Carbohydrates as Organic Raw Materials". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.n05_n07. ISBN 978-3-527-30673-2.
  • Zverlov W, Berezina O, Velikodvorskaya GA, Schwarz WH (August 2006). "Bacterial acetone and butanol production by industrial fermentation in the Soviet Union: use of hydrolyzed agricultural waste for biorefinery". Applied Microbiology and Biotechnology. 71 (5): 587–97. doi:10.1007/s00253-006-0445-z. PMID 16685494. S2CID 24074264.
  • Ahmed J, Swain AK, Das A, Govindarajan R, Bhunia M, Mandal SK (14 November 2019). "A K-arylacetylide complex for catalytic terminal alkyne functionalization using KOtBu as a precatalyst". Chemical Communications. 55 (92): 13860–13863. doi:10.1039/C9CC07833A. ISSN 1364-548X. PMID 31670328. S2CID 204974842.
  • Brown GW (1971). "Displacement of Hydroxyl Groups". The Hydroxyl Group (1971). PATai's Chemistry of Functional Groups. pp. 593–639. doi:10.1002/9780470771259.ch11. ISBN 978-0-470-77125-9.
  • Gessner T, Mayer U (2000). "Triarylmethane and Diarylmethane Dyes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a27_179. ISBN 978-3527306732.

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iupac.org

goldbook.iupac.org

  • "alcohols". IUPAC Gold Book. 2014. doi:10.1351/goldbook.A00204. Retrieved 16 December 2013.
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Alcohols". doi:10.1351/goldbook.A00204

msu.edu

cem.msu.edu

  • William Reusch. "Alcohols". VirtualText of Organic Chemistry. Archived from the original on 19 September 2007. Retrieved 14 September 2007.

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  • WO1994012457A1, Babler, James H., "Process for preparing tertiary alkynols", issued 1994-06-09 

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web.archive.org

  • William Reusch. "Alcohols". VirtualText of Organic Chemistry. Archived from the original on 19 September 2007. Retrieved 14 September 2007.

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