Ácido glioxílico (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ácido glioxílico" in Spanish language version.

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archive.org

Escher CL, Widmer F (1997). «Lipid mobilization and gluconeogenesis in plants: do glyoxylate cycle enzyme activities constitute a real cycle? A hypothesis». Biol Chem. 378 (8): 803-813. PMID 9377475.

docs.google.com

Kamlet, Jonas; and Mathieson, Olin (1953). Manufacture of vanillin and its homologues U.S. Patent 2,640,083. U.S. Patent Office.

doi.org

dx.doi.org

Georges Mattioda and Yani Christidis “Glyoxylic Acid” Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. doi 10.1002/14356007.a12_495
Ip, H. S. Simon; Huang, X. H. Hilda; Yu, Jian Zhen. «Effective Henry's law constants of glyoxal, glyoxylic acid, and glycolic acid». Geophysical Research Letters 36 (1). doi:10.1029/2008GL036212.
Tafel, Julius; and Friedrichs, Gustav (1904). «Elektrolytische Reduction von Carbonsäuren und Carbonsäureestern in schwefelsaurer Lösung». Berichte der deutschen chemischen Gesellschaft 37 (3): 3187-3191. doi:10.1002/cber.190403703116. Consultado el 19 de diciembre de 2013.
Fatiadi, Alexander; and Schaffer, Robert (1974). «An Improved Procedure for Synthesis of DL-4-Hydroxy-3-methoxymandelic Acid (DL-"Vanillyl"-mandelic Acid, VMA)». Journal of Research of the National Bureau of Standards - A. Physics and Chemistry. 78A (3): 411-412. doi:10.6028/jres.078A.024. Consultado el 19 de diciembre de 2013.
Anderson SE1, Ham JE, Munson AE. (2008). «Irritancy and Sensitization Potential of Glyoxylic Acid». J Immunotoxicol. 5(2):93-8. PMID 18569377. doi:10.1080/15476910802085681. Consultado el 14-9-16.

nih.gov

ncbi.nlm.nih.gov

Holms WH (1987). «Control of flux through the citric acid cycle and the glyoxylate bypass in Escherichia coli». Biochem Soc Symp. 54: 17-31. PMID 3332993.
Escher CL, Widmer F (1997). «Lipid mobilization and gluconeogenesis in plants: do glyoxylate cycle enzyme activities constitute a real cycle? A hypothesis». Biol Chem. 378 (8): 803-813. PMID 9377475.
Anderson SE1, Ham JE, Munson AE. (2008). «Irritancy and Sensitization Potential of Glyoxylic Acid». J Immunotoxicol. 5(2):93-8. PMID 18569377. doi:10.1080/15476910802085681. Consultado el 14-9-16.

nist.gov

webbook.nist.gov

Número CAS

nvlpubs.nist.gov

Fatiadi, Alexander; and Schaffer, Robert (1974). «An Improved Procedure for Synthesis of DL-4-Hydroxy-3-methoxymandelic Acid (DL-"Vanillyl"-mandelic Acid, VMA)». Journal of Research of the National Bureau of Standards - A. Physics and Chemistry. 78A (3): 411-412. doi:10.6028/jres.078A.024. Consultado el 19 de diciembre de 2013.

psu.edu

research.chem.psu.edu

pKa Data Compiled by R. Williams, «Copia archivada». Archivado desde el original el 2 de junio de 2010. Consultado el 2 de junio de 2010. .

sciencemadness.org

Cohen, Julius (1920). Practical Organic Chemistry 2nd Ed.. Londres: Macmillan and Co. Limited. pp. 102-104.

tandfonline.com

Anderson SE1, Ham JE, Munson AE. (2008). «Irritancy and Sensitization Potential of Glyoxylic Acid». J Immunotoxicol. 5(2):93-8. PMID 18569377. doi:10.1080/15476910802085681. Consultado el 14-9-16.

web.archive.org

pKa Data Compiled by R. Williams, «Copia archivada». Archivado desde el original el 2 de junio de 2010. Consultado el 2 de junio de 2010. .

wiley.com

onlinelibrary.wiley.com

Tafel, Julius; and Friedrichs, Gustav (1904). «Elektrolytische Reduction von Carbonsäuren und Carbonsäureestern in schwefelsaurer Lösung». Berichte der deutschen chemischen Gesellschaft 37 (3): 3187-3191. doi:10.1002/cber.190403703116. Consultado el 19 de diciembre de 2013.

zirchrom.com

Dissociation Constants Of Organic Acids and Bases (600 compounds), http://zirchrom.com/organic.htm.