Hantzschova syntéza pyridinů (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hantzschova syntéza pyridinů" in Czech language version.

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Jie Jack Li. Name reactions in heterocyclic chemistry. [s.l.]: [s.n.], 2004-10-11. Dostupné online. ISBN 0-471-30215-5. S. 304.

doi.org

dx.doi.org

A. Hantzsch. Condensationprodukte aus Aldehydammoniak und Ketonartigen Verbindungen. Chemische Berichte. 1881, s. 1637–1638. Dostupné online. DOI 10.1002/cber.18810140214.
J. J. Xia; G. W. Wang. One-Pot Synthesis and Aromatization of 1,4-Dihydropyridines in Refluxing Water. Synthesis. 2005, s. 2379–2383. DOI 10.1055/s-2005-870022.
J. J. van den Eynde; A. Mayence. Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview. Molecules. 2003, s. 381–391. Dostupné online. DOI 10.3390/80400381.
Vanessa G. Santos. The Multicomponent Hantzsch Reaction: Comprehensive Mass Spectrometry Monitoring Using Charge-Tagged Reagants. Chemistry – A European Journal. 2014, s. 12808–12816. DOI 10.1002/chem.201303065. PMID 25179028.
Alan R. Katrinsky; Daryl L. Ostercamp; Taher I. Yousaf. The mechanism of the hantzsch pyridine synthesis: A study by ¹⁵N and ¹³C NMR spectroscopy. Tetrahedron. 1986, s. 5729–5738. Dostupné online. DOI 10.1016/S0040-4020(01)88178-3.
Atul Kumar. ChemInform Abstract: Efficient Synthesis of Hantzsch Esters and Polyhydroquinoline Derivatives in Aqueous Micelles.Chybí název periodika! 2008-08-05. DOI 10.1002/chin.200832145.
Sabir H. Mashraqui. Bismuth Nitrate Pentahydrate: A Convenient Reagent for the Oxidation of Hantzsch 1,4-Dihydropyridines. Synthesis. 1998, s. 713–714. DOI 10.1055/s-1998-4516.
Jhillu S. Yadav. Aromatization of Hantzsch 1,4-Dihydropyridines with I₂-MeOH. Synthesis. 2000, s. 1532–1534. DOI 10.1055/s-2000-7613.
Kwang-Youn Ko. Aromatization of Hantzsch 1,4-Dihydropyridines with Magtrieve. Tetrahedron Letters. 1999, s. 3207–3208. DOI 10.1016/S0040-4039(99)00467-0.
Xiali Liao. Oxidative aromatization of Hantzsch 1,4-dihydropyridines by sodium chlorite. Tetrahedron Letters. 2010, s. 3859–3861. DOI 10.1016/j.tetlet.2010.05.091.
Xiaojing Wei. Metal-Free-Mediated Oxidation Aromatization of 1,4-Dihydropyridines to Pyridines Using Visible Light and Air. Chinese Journal of Chemistry. 2014, s. 1245–1250. DOI 10.1002/cjoc.201400521.
E. Knoevenagel; A. Fries. Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese. Berichte der Deutschen Chemischen Gesellschaft. 1898, s. 761–767. Dostupné online. DOI 10.1002/cber.189803101157.

elsevier.com

linkinghub.elsevier.com

Alan R. Katrinsky; Daryl L. Ostercamp; Taher I. Yousaf. The mechanism of the hantzsch pyridine synthesis: A study by ¹⁵N and ¹³C NMR spectroscopy. Tetrahedron. 1986, s. 5729–5738. Dostupné online. DOI 10.1016/S0040-4020(01)88178-3.

mdpi.org

J. J. van den Eynde; A. Mayence. Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview. Molecules. 2003, s. 381–391. Dostupné online. DOI 10.3390/80400381.

nih.gov

ncbi.nlm.nih.gov

Vanessa G. Santos. The Multicomponent Hantzsch Reaction: Comprehensive Mass Spectrometry Monitoring Using Charge-Tagged Reagants. Chemistry – A European Journal. 2014, s. 12808–12816. DOI 10.1002/chem.201303065. PMID 25179028.

niscair.res.in

nopr.niscair.res.in

Anil Saini. Hantzsch reaction: Recent advances in Hantzsch 1,4-dihydropyridines. Journal of Scientific and Industrial Research. 2008, s. 95–111. Dostupné online.

zenodo.org

A. Hantzsch. Condensationprodukte aus Aldehydammoniak und Ketonartigen Verbindungen. Chemische Berichte. 1881, s. 1637–1638. Dostupné online. DOI 10.1002/cber.18810140214.
E. Knoevenagel; A. Fries. Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese. Berichte der Deutschen Chemischen Gesellschaft. 1898, s. 761–767. Dostupné online. DOI 10.1002/cber.189803101157.