Abstract
This review highlights the pyridinium salts in terms of their natural occurrence, synthesis, reactivity, biological properties, and diverse applications.
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References
386
[1]
Laville Pure Appl. Chem. (2009) 10.1351/pac-con-08-11-14
[2]
Temraz BMC Pharmacol. (2006) 10.1186/1471-2210-6-10
[3]
Zhang Proc. Natl. Acad. Sci. U. S. A. (1991) 10.1073/pnas.88.23.10407
[4]
Dasari Microbiol. Res. (2012) 10.1016/j.micres.2011.12.003
[5]
Mancini Org. Biomol. Chem. (2004) 10.1039/b400782d
[6]
Laville Molecules (2009) 10.3390/molecules14114716
[7]
Reyes Tetrahedron (2007) 10.1016/j.tet.2007.01.013
[8]
Sepcik J. Toxicol. (2000)
[9]
R. J. Andersen , R. W.Van Soest and F.Kong , Alkaloids Chemical and Biological Perspectives , ed. S. W. Pelletier , Elsevier Science , Oxford, UK , 1996 , vol. 10 , p. 301 10.1016/s0735-8210(96)80027-6
[10]
Welton Chem. Rev. (1999) 10.1021/cr980032t
[11]
P. Wasserscheid and T.Welton , Ionic Liquids in Synthesis , Wiley-VCH , Weinheim, Germany , 2nd edn, 2008
[12]
Salomaa Acta Chem. Scand. (1957) 10.3891/acta.chem.scand.11-0468
[13]
Pernak Pol. J. Chem. (1981)
[14]
Pernak Pol. J. Chem. (1985)
[15]
R. E. Lyle , in Pyridine and its Derivatives , Wiley , New York, NY , 1974 , vol. 1 , p. 137
[16]
Goldman Angew. Chem., Int. Ed. Engl. (1991) 10.1002/anie.199115591
[17]
Sunkel J. Med. Chem. (1990) 10.1021/jm00174a017
[18]
Jaing J. Med. Chem. (1999) 10.1021/jm980688e
[19]
Luo Org. Lett. (2015) 10.1021/acs.orglett.5b00028
[20]
Nolsoe J. Org. Chem. (2015) 10.1021/acs.joc.5b00879
[21]
W. Śliwa , N-Substituted Salts of Pyridine and Related Compounds, Synthesis, Properties, Applications , Academic Press , Częstochowa, Poland , 1996
[22]
Coe Adv. Funct. Mater. (2003) 10.1002/adfm.200300026
[23]
E. V. Dehmlow and S. S.Dehmlow , Phase Transfer Catalysis , Verlag Chemie , Weinheim, Germany , 2nd edn, 1983
[24]
Scriven Chem. Soc. Rev. (1983) 10.1039/cs9831200129
[25]
Madaan J. Oleo Sci. (2008) 10.5650/jos.57.197
[26]
Laville Eur. J. Org. Chem. (2008) 10.1002/ejoc.200700741
[27]
Suzuki Tetrahedron (2015) 10.1016/j.tet.2015.01.064
[28]
Bennasar J. Org. Chem. (1999) 10.1021/jo9911894
[29]
Bennasar Tetrahedron: Asymmetry (2002) 10.1016/s0957-4166(02)00055-1
[30]
Focken Org. Lett. (2006) 10.1021/ol0609006
[31]
Azzouz J. Org. Chem. (2008) 10.1021/jo702141b
[32]
Kuethe J. Org. Chem. (2004) 10.1021/jo049724+
[33]
Bennasar J. Org. Chem. (2002) 10.1021/jo026173j
[34]
Bennasar J. Org. Chem. (1997) 10.1021/jo9623301
[35]
Schoene Biochem. Pharmacol. (1976) 10.1016/0006-2952(76)90049-6
[36]
Zhu Bioconjugate Chem. (2008) 10.1021/bc8004039
[37]
Tucker Biochim. Biophys. Acta (2003) 10.1016/s0005-2736(03)00175-5
[38]
Lim Tetrahedron Lett. (1997) 10.1016/s0040-4039(97)00574-1
[39]
Kondo J. Chem. Soc., Perkin Trans. 2 (1984) 10.1039/p29840002093
[40]
Castejon J. Am. Chem. Soc. (1999) 10.1021/ja983736t
[41]
R. A. Abramovitch and E.Klingsberg , Pyridine and Its Derivatives , Supplement , Wiley, New York , 1974
[42]
Pernak ARKIVOC (2000) 10.3998/ark.5550190.0001.606
[43]
Marek Molecules (2010) 10.3390/molecules15031967
[44]
Wong Tetrahedron Lett. (1994) 10.1016/s0040-4039(00)75796-0
[45]
Mehmandoust J. Chem. Soc., Chem. Commun. (1989) 10.1039/c39890001185
[46]
Diez Heterocycles (1991) 10.3987/com-91-5817
[47]
Comins J. Am. Chem. Soc. (1994) 10.1021/ja00090a019
[48]
Palin Bioorg. Med. Chem. Lett. (2002) 10.1016/s0960-894x(02)00483-3
[49]
Kost Tetrahedron (1981) 10.1016/s0040-4020(01)98858-1
[50]
Zincke Ann. Chim. (1904) 10.1002/jlac.19043330212

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Published
Jan 01, 2018
Vol/Issue
5(3)
Pages
453-493
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Funding
Fundação para a Ciência e a Tecnologia Award: COMPETE Programme (SAICTPAC/0019/2015)
Cite This Article
Subbiah Sowmiah, José M. S. S. Esperança, Luís P. N. Rebelo, et al. (2018). Pyridinium salts: from synthesis to reactivity and applications. Organic Chemistry Frontiers, 5(3), 453-493. https://doi.org/10.1039/c7qo00836h