Hantzsch pyridine synthesis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hantzsch pyridine synthesis" in English language version.

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14doi.org

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3nih.gov

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2zenodo.org

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1mdpi.org

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doi.org

Hantzsch, A. (1881). "Condensationprodukte aus Aldehydammoniak und Ketonartigen Verbindungen". Chemische Berichte. 14 (2): 1637–8. doi:10.1002/cber.18810140214.
Xia, J. J.; Wang, G. W. (2005). "One-Pot Synthesis and Aromatization of 1,4-Dihydropyridines in Refluxing Water". Synthesis. 2005 (14): 2379–83. doi:10.1055/s-2005-870022.
van den Eynde, J. J.; Mayence, A. (2003). "Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview" (PDF). Molecules. 8 (4): 381–91. doi:10.3390/80400381. S2CID 98443099.
Santos, Vanessa G. (2014). "The Multicomponent Hantzsch Reaction: Comprehensive Mass Spectrometry Monitoring Using Charge-Tagged Reagants". Chemistry – A European Journal. 20 (40): 12808–12816. doi:10.1002/chem.201303065. PMID 25179028.
Katrinsky, Alan R.; Ostercamp, Daryl L.; Yousaf, Taher I. (1986). "The mechanism of the hantzsch pyridine synthesis: A study by ¹⁵N and ¹³C NMR spectroscopy". Tetrahedron. 42 (20): 5729–5738. doi:10.1016/S0040-4020(01)88178-3.
Kumar, Atul (5 August 2008). "ChemInform Abstract: Efficient Synthesis of Hantzsch Esters and Polyhydroquinoline Derivatives in Aqueous Micelles". ChemInform. 39 (32). doi:10.1002/chin.200832145.
Mashraqui, Sabir H. (1998). "Bismuth Nitrate Pentahydrate: A Convenient Reagent for the Oxidation of Hantzsch 1,4-Dihydropyridines". Synthesis. 1998 (5): 713–714. doi:10.1055/s-1998-4516.
Yadav, Jhillu S. (2000). "Aromatization of Hantzsch 1,4-Dihydropyridines with I₂-MeOH". Synthesis. 2000 (11): 1532–1534. doi:10.1055/s-2000-7613.
Ko, Kwang-Youn (1999). "Aromatization of Hantzsch 1,4-Dihydropyridines with Magtrieve". Tetrahedron Letters. 40: 3207–3208. doi:10.1016/S0040-4039(99)00467-0.
Liao, Xiali (2010). "Oxidative aromatization of Hantzsch 1,4-dihydropyridines by sodium chlorite". Tetrahedron Letters. 51 (29): 3859–3861. doi:10.1016/j.tetlet.2010.05.091. S2CID 94650170.
Wei, Xiaojing (2014). "Metal-Free-Mediated Oxidation Aromatization of 1,4-Dihydropyridines to Pyridines Using Visible Light and Air". Chinese Journal of Chemistry. 32 (12): 1245–1250. doi:10.1002/cjoc.201400521.
Jassem, Ahmed Majeed; Almashal, Faeza Abdul Kareem; Mohammed, Mohammed Qasim; Jabir, Hadi Abdal Samad (7 February 2020). "A catalytic and green method for one-pot synthesis of new Hantzsch 1,4-dihydropyridines". SN Applied Sciences. 2 (3). doi:10.1007/s42452-020-2165-x.
Sharma, M.G; Rajani, D.P.; Patel, H.M. (14 June 2017). "Green approach for synthesis of bioactive Hantzsch 1,4-dihydropyridine derivatives based on thiophene moiety via multicomponent reaction". Royal Society Open Science. 4 (6): 170006. Bibcode:2017RSOS....470006S. doi:10.1098/rsos.170006. PMC 5493906. PMID 28680664.
Knoevenagel, E.; Fries, A. (1898). "Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese". Berichte der Deutschen Chemischen Gesellschaft. 31 (1): 761–7. doi:10.1002/cber.189803101157.

elsevier.com

linkinghub.elsevier.com

Katrinsky, Alan R.; Ostercamp, Daryl L.; Yousaf, Taher I. (1986). "The mechanism of the hantzsch pyridine synthesis: A study by ¹⁵N and ¹³C NMR spectroscopy". Tetrahedron. 42 (20): 5729–5738. doi:10.1016/S0040-4020(01)88178-3.

harvard.edu

ui.adsabs.harvard.edu

Sharma, M.G; Rajani, D.P.; Patel, H.M. (14 June 2017). "Green approach for synthesis of bioactive Hantzsch 1,4-dihydropyridine derivatives based on thiophene moiety via multicomponent reaction". Royal Society Open Science. 4 (6): 170006. Bibcode:2017RSOS....470006S. doi:10.1098/rsos.170006. PMC 5493906. PMID 28680664.

mdpi.org

van den Eynde, J. J.; Mayence, A. (2003). "Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview" (PDF). Molecules. 8 (4): 381–91. doi:10.3390/80400381. S2CID 98443099.

nih.gov

pubmed.ncbi.nlm.nih.gov

Santos, Vanessa G. (2014). "The Multicomponent Hantzsch Reaction: Comprehensive Mass Spectrometry Monitoring Using Charge-Tagged Reagants". Chemistry – A European Journal. 20 (40): 12808–12816. doi:10.1002/chem.201303065. PMID 25179028.
Sharma, M.G; Rajani, D.P.; Patel, H.M. (14 June 2017). "Green approach for synthesis of bioactive Hantzsch 1,4-dihydropyridine derivatives based on thiophene moiety via multicomponent reaction". Royal Society Open Science. 4 (6): 170006. Bibcode:2017RSOS....470006S. doi:10.1098/rsos.170006. PMC 5493906. PMID 28680664.

ncbi.nlm.nih.gov

Sharma, M.G; Rajani, D.P.; Patel, H.M. (14 June 2017). "Green approach for synthesis of bioactive Hantzsch 1,4-dihydropyridine derivatives based on thiophene moiety via multicomponent reaction". Royal Society Open Science. 4 (6): 170006. Bibcode:2017RSOS....470006S. doi:10.1098/rsos.170006. PMC 5493906. PMID 28680664.

niscair.res.in

nopr.niscair.res.in

Saini, Anil (February 2008). "Hantzsch reaction: Recent advances in Hantzsch 1,4-dihydropyridines" (PDF). Journal of Scientific and Industrial Research. 67: 95–111.

semanticscholar.org

api.semanticscholar.org

van den Eynde, J. J.; Mayence, A. (2003). "Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview" (PDF). Molecules. 8 (4): 381–91. doi:10.3390/80400381. S2CID 98443099.
Liao, Xiali (2010). "Oxidative aromatization of Hantzsch 1,4-dihydropyridines by sodium chlorite". Tetrahedron Letters. 51 (29): 3859–3861. doi:10.1016/j.tetlet.2010.05.091. S2CID 94650170.

zenodo.org

Hantzsch, A. (1881). "Condensationprodukte aus Aldehydammoniak und Ketonartigen Verbindungen". Chemische Berichte. 14 (2): 1637–8. doi:10.1002/cber.18810140214.
Knoevenagel, E.; Fries, A. (1898). "Synthesen in der Pyridinreihe. Ueber eine Erweiterung der Hantzsch'schen Dihydropyridinsynthese". Berichte der Deutschen Chemischen Gesellschaft. 31 (1): 761–7. doi:10.1002/cber.189803101157.