1,4-ciclohexanodiol (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "1,4-ciclohexanodiol" in Spanish language version.

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3patents.google.com

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acs.org

pubs.acs.org

Bonnet, M.; Geneste, P.; Rodriguez, M. (1980). «Liquid-phase catalytic hydrogenation of 1,4-cyclohexanedione: activity and selectivity». Journal of Organic Chemistry 45 (1): 40-43. Consultado el 24 de octubre de 2018.
Lam, K.; Markó, I.E. (2009). «Chemoselective Chemical and Electrochemical Deprotections of Aromatic Esters». Organic Letters 11 (13): 2752-2755. Consultado el 24 de octubre de 2018.

chemspider.com

1,4-Cyclohexanediol (ChemSpider)

fishersci.com

1,4-Cyclohexanediol, mixture of cis and trans. Safety Data Sheet (ThermoFisher)

jst.go.jp

jstage.jst.go.jp

Kamochi, Y.; Kudo, T.; Masuda, T.; Takadate, A. (2005). «Facile Deoxygenation of Dicarbonyl Compounds Using a Samarium Diiodide–Additive System». Chemical and Pharmaceutical Bulletin 53 (8): 1017-1020. Consultado el 24 de octubre de 2018.

molbase.com

nih.gov

pubchem.ncbi.nlm.nih.gov

1,4-Cyclohexanediol (PubChem)

ncbi.nlm.nih.gov

Li, N.; Jia, W.; Zhang, Y.; Tan, F.; Zhang, J. (2011). «Synergistic effect of 1,4-cyclohexanediol and 1,2-hexanediol on percutaneous absorption and penetration of metronidazole». Int. J .Pharm. 415 (1-2): 169-174. Consultado el 24 de septiembre de 2018.

nist.gov

webbook.nist.gov

Número CAS

patents.google.com

sciencedirect.com

Kamochi, Y.; Kudo, T. (1994). «Novel and facile reduction of phenol derivatives with samarium diiodide-base system». Tetrahedron Letters 35 (24): 4169-4172. Consultado el 24 de octubre de 2018.
Fischer, A; Mallat, T; Baiker, A. (1999). «Synthesis of 1,4-Diaminocyclohexane in Supercritical Ammonia». Journal of Catalysis 182 (2): 289-291. Consultado el 7 de junio de 2016.

springer.com

link.springer.com

Li, N.; Jia, W.; Zhang, Y.;, Zhang, M.C.; Tan, F.; Zhang, J. (2014). «Effect of Hydrocarbon Chain Length in 1,2-Alkanediols on Percutaneous Absorption of Metronidazole: Toward Development of a General Vehicle for Controlled Release». AAPS PharmSciTech 15 (2): 354-363. Consultado el 29 de septiembre de 2018.

tandfonline.com

Rostami, A.; Ahmad-Jangi, F.; Zarebin, M.R.; Akradi, J. (2010). «Green and Efficient Procedure for the Trimethylsilylation of Hydroxy Groups and Their Regeneration Using Sulfamic Acid as Recyclable Catalyst». Synthetic Communications 40 (10): 1500-1507. Consultado el 24 de octubre de 2018.