Diethylazodikarboxylát (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Diethylazodikarboxylát" in Czech language version.

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archive.org

W. L. F. Armarego. Purification of laboratory chemicals. [s.l.]: Butterworth-Heinemann, 2009-05-22. Dostupné online. ISBN 978-1-85617-567-8. S. 124-.

doi.org

dx.doi.org

Fumio Yoneda; Kunio Suzuki; Yoshihiro Nitta. A new hydrogen-abstracting reaction with diethyl azodicarboxylate. The Journal of Organic Chemistry. 1967, s. 727–729. ISSN 0022-3263. DOI 10.1021/jo01278a049.
Eric J. Stoner; Amy C. Hart. Encyclopedia of Reagents for Organic Synthesis, 8 Volume Set. [s.l.]: [s.n.], 2010. ISBN 978-0471936237. DOI 10.1002/047084289X.rd176.pub2. Kapitola Diethyl Azodicarboxylate.
Rabjohn, N. Diethyl azodicarboxylate. Organic Syntheses. 1948, s. 58. DOI 10.15227/orgsyn.028.0058.
O. Mitsunobu; Y. Yamada. Preparation of Esters of Carboxylic and Phosphoric Acid via Quaternary Phosphonium Salts. Bulletin of the Chemical Society of Japan. 1967, s. 2380–2382. DOI 10.1246/bcsj.40.2380.
Oyo Mitsunobu. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products. Synthesis. 1981, s. 1–28. DOI 10.1055/s-1981-29317.
CZERNECKI, Stanislas; VALÉRY, Jean-Marc. An Efficient Synthesis of 3′-Azido-3′-deoxythymidine (AZT). Synthesis. 1991, s. 239. DOI 10.1055/s-1991-26434.
Kim L. Dueholm; Youssef L. Aly; Per T. Jørgensen; Ahmed A. El-Barbary; Erik B. Pedersen; Claus Nielsen. Convergent synthesis of 2′,3′-dideoxy-3′-methylthio and 2′,3′-dideoxy-3′-mercapto nucleosides and their disulfide analogues — Potential anti-HIV agents. Monatshefte für Chemie - Chemical Monthly. 1993, s. 37–53. DOI 10.1007/BF00808508.
David Farquhar; Saeed Khan; Devendra N. Srivastva; Priscilla P. Saunders. Synthesis and Antitumor Evaluation of Bis[(pivaloyloxy)methyl] 2'-Deoxy-5-fluorouridine 5'-Monophosphate (FdUMP): A Strategy To Introduce Nucleotides into Cells. Journal of Medicinal Chemistry. 1994, s. 3902–3909. DOI 10.1021/jm00049a009. PMID 7966151.
Ionic and Covalent Copper(II)-Based Catalysts for Michael Additions. The Mechanism. The Journal of Organic Chemistry. 2004, s. 6834–6842. DOI 10.1021/jo049373z. PMID 15387609.
Takeshi Uemura. Copper Salt Catalyzed Addition of Arylboronic Acids to Azodicarboxylates. The Journal of Organic Chemistry. 2005, s. 8631. DOI 10.1021/jo051387x. PMID 16209627.
P. G. Gassman. Bicyclo[2.1.0]pentane. Organic Syntheses. 1969, s. 1. ISSN 0078-6209. DOI 10.15227/orgsyn.049.0001.
Min Shi. Aza-Baylis–Hillman reactions of diisopropyl azodicarboxylate or diethyl azodicarboxylate with acrylates and acrylonitrile. Tetrahedron. 2004, s. 2083–2089. DOI 10.1016/j.tet.2003.12.059.
Vijay Nair; Akkattu T. Biju. A Novel Reaction of the "Huisgen Zwitterion" with Chalcones and Dienones: An Efficient Strategy for the Synthesis of Pyrazoline and Pyrazolopyridazine Derivatives. Angewandte Chemie International Edition. 2007, s. 2070–2073. DOI 10.1002/anie.200604025. PMID 17286329.

nih.gov

ncbi.nlm.nih.gov

David Farquhar; Saeed Khan; Devendra N. Srivastva; Priscilla P. Saunders. Synthesis and Antitumor Evaluation of Bis[(pivaloyloxy)methyl] 2'-Deoxy-5-fluorouridine 5'-Monophosphate (FdUMP): A Strategy To Introduce Nucleotides into Cells. Journal of Medicinal Chemistry. 1994, s. 3902–3909. DOI 10.1021/jm00049a009. PMID 7966151.
Ionic and Covalent Copper(II)-Based Catalysts for Michael Additions. The Mechanism. The Journal of Organic Chemistry. 2004, s. 6834–6842. DOI 10.1021/jo049373z. PMID 15387609.
Takeshi Uemura. Copper Salt Catalyzed Addition of Arylboronic Acids to Azodicarboxylates. The Journal of Organic Chemistry. 2005, s. 8631. DOI 10.1021/jo051387x. PMID 16209627.
Vijay Nair; Akkattu T. Biju. A Novel Reaction of the "Huisgen Zwitterion" with Chalcones and Dienones: An Efficient Strategy for the Synthesis of Pyrazoline and Pyrazolopyridazine Derivatives. Angewandte Chemie International Edition. 2007, s. 2070–2073. DOI 10.1002/anie.200604025. PMID 17286329.

pubchem.ncbi.nlm.nih.gov

Diethoxycarbonyldiazene. pubchem.ncbi.nlm.nih.gov [online]. PubChem [cit. 2021-05-24]. Dostupné online. (anglicky)

orgsyn.org

KAUER, J. C. Diethyl azodicarboxylate. Org. Synth.. Dostupné online. ; Coll. Vol.. S. 411.

ox.ac.uk

msds.chem.ox.ac.uk

Safety (MSDS) data for diethyl azodicarboxylate Archivováno 9. 12. 2010 na Wayback Machine. Msds.chem.ox.ac.uk. Retrieved on 2011-03-15
Safety (MSDS) data for diethyl azodicarboxylate Archivováno 9. 12. 2010 na Wayback Machine.. Msds.chem.ox.ac.uk. Retrieved on 2011-03-15.

tamu.edu

repository.tamu.edu

Kelmara K. Kelly (2009) Novel isotope effects and organic reaction mechanisms, PhD thesis, Texas A&M University, p. 81

web.archive.org

Safety (MSDS) data for diethyl azodicarboxylate Archivováno 9. 12. 2010 na Wayback Machine. Msds.chem.ox.ac.uk. Retrieved on 2011-03-15
Safety (MSDS) data for diethyl azodicarboxylate Archivováno 9. 12. 2010 na Wayback Machine.. Msds.chem.ox.ac.uk. Retrieved on 2011-03-15.

worldcat.org

Fumio Yoneda; Kunio Suzuki; Yoshihiro Nitta. A new hydrogen-abstracting reaction with diethyl azodicarboxylate. The Journal of Organic Chemistry. 1967, s. 727–729. ISSN 0022-3263. DOI 10.1021/jo01278a049.
P. G. Gassman. Bicyclo[2.1.0]pentane. Organic Syntheses. 1969, s. 1. ISSN 0078-6209. DOI 10.15227/orgsyn.049.0001.