Diol (English Wikipedia)

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

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chemistrysteps.com

Gevorg, Dr S. (2021-11-22). "Diols: Nomenclature, Preparation, and Reactions". Chemistry Steps. Retrieved 2024-04-15.
Gevorg, Dr S. (2021-11-22). "Diols: Nomenclature, Preparation, and Reactions". Chemistry Steps. Retrieved 2024-04-15.

doi.org

doi.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "diols". doi:10.1351/goldbook.D01748.
Advantages of Synthesizing trans-1,2-Cyclohexanediol in a Continuous Flow Microreactor over a Standard Glass Apparatus Andreas Hartung, Mark A. Keane, and Arno Kraft J. Org. Chem. 2007, 72, 10235–10238 doi:10.1021/jo701758p.
Blomquist, A. T.; Goldstein, Albert (1956). "1,2-Cyclodecanediol". Organic Syntheses. 36: 12. doi:10.15227/orgsyn.036.0012.
Bode, Silke E.; Wolberg, Michael; Müller, Michael (2006). "Stereoselective Synthesis of 1,3-Diols". Synthesis (in German). 2006 (4): 557–588. doi:10.1055/s-2006-926315. ISSN 0039-7881.
Werle, Peter; Morawietz, Marcus; Lundmark, Stefan; Sörensen, Kent; Karvinen, Esko; Lehtonen, Juha (2008). "Alcohols, Polyhydric". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_305.pub2. ISBN 978-3527306732.
Angewandte Chemie International Edition in English. Wiley. doi:10.1002/(issn)1521-3773a.

dx.doi.org

Angewandte Chemie International Edition in English. Wiley. doi:10.1002/(issn)1521-3773a.

google.co.in

March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 3rd edition, New York: Wiley, ISBN 9780471854722, OCLC 642506595.

iupac.org

goldbook.iupac.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "diols". doi:10.1351/goldbook.D01748.

nih.gov

ncbi.nlm.nih.gov

Manabe, Shino (2021), Nishihara, Shoko; Angata, Kiyohiko; Aoki-Kinoshita, Kiyoko F.; Hirabayashi, Jun (eds.), "Benzylidene protection of diol", Glycoscience Protocols (GlycoPODv2), Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology, PMID 37590710, retrieved 2024-04-14

pubmed.ncbi.nlm.nih.gov

Manabe, Shino (2021), Nishihara, Shoko; Angata, Kiyohiko; Aoki-Kinoshita, Kiyoko F.; Hirabayashi, Jun (eds.), "Benzylidene protection of diol", Glycoscience Protocols (GlycoPODv2), Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology, PMID 37590710, retrieved 2024-04-14

organic-chemistry.org

"Carbonyl Protecting Groups - Stability". www.organic-chemistry.org. Retrieved 2024-04-15.
"Zirconium Tetrachloride (ZrCl4) Catalyzed Highly Chemoselective and Efficient Acetalization of Carbonyl Compounds". www.organic-chemistry.org. Retrieved 2024-04-14.

orgsynth.org

trans-cyclohexanediol Organic Syntheses, Coll. Vol. 3, p. 217 (1955); Vol. 28, p.35 (1948) http://www.orgsynth.org/orgsyn/pdfs/CV3P0217.pdf.

thieme-connect.de

Bode, Silke E.; Wolberg, Michael; Müller, Michael (2006). "Stereoselective Synthesis of 1,3-Diols". Synthesis (in German). 2006 (4): 557–588. doi:10.1055/s-2006-926315. ISSN 0039-7881.

ucla.edu

chem.ucla.edu

"Illustrated Glossary of Organic Chemistry - Glycol". www.chem.ucla.edu. Retrieved 2024-04-15.

worldcat.org

search.worldcat.org

March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 3rd edition, New York: Wiley, ISBN 9780471854722, OCLC 642506595.
Bode, Silke E.; Wolberg, Michael; Müller, Michael (2006). "Stereoselective Synthesis of 1,3-Diols". Synthesis (in German). 2006 (4): 557–588. doi:10.1055/s-2006-926315. ISSN 0039-7881.