2-merkaptoetanol (Slovak Wikipedia)

Analysis of information sources in references of the Wikipedia article "2-merkaptoetanol" in Slovak language version.

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1merckmillipore.com

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1organic-chemistry.org

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1chemicalland21.com

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archive.org

Nelson, David R.; Lehninger, Albert L; Cox, Michael. Lehninger principles of biochemistry. New York : W.H. Freeman, 2005. Dostupné online. ISBN 0-7167-4339-6. S. 148.

biopedia.sk

Denaturačná elektroforéza proteínov v polyakrylamidovom géli (SDS-PAGE) [online]. Biopedia.sk, [cit. 2023-01-19]. Dostupné online.

chemicalland21.com

2-Mercaptoethanol [online]. Chemicalland21.com. Dostupné online. Archivované 2006-10-05 z originálu.

doi.org

dx.doi.org

ROY, Kathrin-maria. Thiols and Organic Sulfides. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2000-06-15. Dostupné online. DOI:10.1002/14356007.a26_767 (po anglicky)
Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis. Chem. Rev., 2004, s. 199–250. DOI: 10.1021/cr0200769. PMID 14719975.
Aitken CE; Marshall RA, Puglisi JD. An oxygen scavenging system for improvement of dye stability in single-molecule fluorescence experiments. Biophys J, 2008, s. 1826–35. DOI: 10.1529/biophysj.107.117689. PMID 17921203.
STEVENS R.; Stevens L.; Price N.C.. The Stabilities of Various Thiol Compounds used in Protein Purifications. Biochemical Education, 1983, s. 70. DOI: 10.1016/0307-4412(83)90048-1.
Properties of the NAD(P)H-dependent xylose reductase from the xylose-fermenting yeast Pichia stipitis. The Biochemical Journal, 1985, s. 669–77. DOI: 10.1042/bj2260669. PMID 3921014.
A Nucleophilic Deprotection of Carbamate Mediated by 2-Mercaptoethanol. Organic Letters, 2022, s. 3736–3740. DOI: 10.1021/acs.orglett.2c01410. PMID 35559611.

hazard.com

Material Safety Data Sheet [online]. JT Baker. Dostupné online.

merckmillipore.com

2-Merkaptoetanol SDS [online]. [Cit. 2023-01-18]. Dostupné online.

nih.gov

ncbi.nlm.nih.gov

Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis. Chem. Rev., 2004, s. 199–250. DOI: 10.1021/cr0200769. PMID 14719975.
Aitken CE; Marshall RA, Puglisi JD. An oxygen scavenging system for improvement of dye stability in single-molecule fluorescence experiments. Biophys J, 2008, s. 1826–35. DOI: 10.1529/biophysj.107.117689. PMID 17921203.
Properties of the NAD(P)H-dependent xylose reductase from the xylose-fermenting yeast Pichia stipitis. The Biochemical Journal, 1985, s. 669–77. DOI: 10.1042/bj2260669. PMID 3921014.
A Nucleophilic Deprotection of Carbamate Mediated by 2-Mercaptoethanol. Organic Letters, 2022, s. 3736–3740. DOI: 10.1021/acs.orglett.2c01410. PMID 35559611.

organic-chemistry.org

1,3-Dithiolanes, 1,3-Dithianes [online]. Organic Chemistry Portal. Dostupné online. Archivované 2008-05-17 z originálu.

web.archive.org

1,3-Dithiolanes, 1,3-Dithianes [online]. Organic Chemistry Portal. Dostupné online. Archivované 2008-05-17 z originálu.
2-Mercaptoethanol [online]. Chemicalland21.com. Dostupné online. Archivované 2006-10-05 z originálu.

wiley.com

onlinelibrary.wiley.com

ROY, Kathrin-maria. Thiols and Organic Sulfides. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2000-06-15. Dostupné online. DOI:10.1002/14356007.a26_767 (po anglicky)