[1]
Mannich, C.; Krosche, W. The Mannich reaction. Arch. Pharm. , 1912, 250, 647-667.
[2]
Blicke, F.F. The Mannich reactions. Org. Reactions., 1942, 1, 303.
[3]
Shen, A.Y.; Tsai, C.T.; Chen, C.L. Synthesis and cardiovascular evaluation of N-substituted-1-aminomethyl-2-naphthols. Eur. J. Med. Chem., 1999, 34, 877.
[4]
Shaterian, H.R.; Yarahmadi, H.; Ghashang, M. An efficient, simple and expedition synthesis of 1-amidoalkyl-2-naphthols as ‘drug-like’ molecules for biological screening. Bioorg. Med. Chem. Lett., 2008, 18, 788-792.
[5]
Sapkal, S.B.; Shelke, K.F.; Madje, B.R.; Shingate, B.B.; Shingare, M.S. 1-Butyl-3-Methyl Imidazolium Hydrogen Sulphate Promoted One-Pot Three-Component Synthesis of AmidoalkylNaphthols. Bull. Korean Chem. Soc., 2009, 30, 2887.
[6]
Patel, H.M. Synthesis, characterization, and applications of some novel mordent and heterocyclic disperse dyes on polyester and wool fibers. Electron. J. Chem., 2012, 4(3), 159-170.
[7]
Patel, H.M. Synthesis, characterization and dyeing behavior of heterocyclic acid dyes and mordant acid dyes on wool and silk fabrics. J. Serbian. Chem. Soc., 2012, 77(11), 1551-1560.
[8]
Patel, H.M. Synthesis, antimicrobial activity and absorption studies of some novel heterocyclic dyes based on 4-hexyl benzene-1,3-diol. European. J. Chem., 2012, 3(1), 44-50.
[9]
Patel, H.M. Synthesis, structure investigation and dyeing assessment of novel bisazo disperse dyes derived from UV absorbing material. IOSR J. Appl. Chem., 2014, 6(5), 51.
[10]
Patel, H.M. Synthesis, characterization and dyeing assessment of novel bisazo-acid dyes derived from 2-hydroxy-4-methoxy- benzophenone-5-sulphonic acid. Int. J. Sci. Eng. Res., 2014, 5(1), 2213-2217.
[11]
Patel, H.M. Solvent-free synthesis of Mannich products catalyzed by ethyl ammonium nitrate as reusable ionic liquid and there in vitro microbial studies. Int. J. Recent Sci. Res, 2014, 5(10), 1799.
[12]
Patel, H.M. Design, synthesis and biological evaluation of new Mannich products using ethyl ammonium nitrate as a reusable ionic liquid. IOSR J. Appl. Chem, 2014, 7(8), 40-47.
[13]
Patel, H.M. Synthesis of new Mannich products bearing quinoline nucleus using reusable ionic liquid and antitubercular evaluation. Green Sustainable Chem, 2015, 5, 107.
[14]
Patel, H.M.; Patel, K.D.; Patel, H.D. Facile synthesis and biological evaluation of new mannich products as potential antibacterial, antifungal, and antituberculosis agents: Molecular docking study. Curr. Bioactive. Compd., 2016, 12, 43.
[15]
Sonwane, S.K.; Srivastava, S.D.; Srivastava, S.K. Synthesis and antimicrobial activity of some 2[(4-substituted-phenyl-3-chloro-azetidin-2-one)-5-(2-methylamino-4-phenyl-l,3-thiazolyl-]-l,3,4-thiadiazoles. J. Sci. I. R. Iran, 2009, 20(3), 227-232.
[16]
Wayne, P.A.
National Committee for Clinical Laboratory Standards: Methods for Dilution, Antimicrobial Susceptibility,
Tests for Bacteria that Grow Aerobically Approved Standard, 9th ed. 2010 (M7`A5)
[17]
Rattan, A. Antimicrobials in Laboratory Medicine; BI Churchill Livingstone: India, 2000, p. 85.
[18]
Sharma, M.G.; Dhanji, R.; Patel, H.M. Green approach for the synthesis of bioactive Hantzsch 1, 4-dihydropyridine derivatives based on thiophene moiety via multicomponent reaction. Royal. Soc. Open Sci., 2017, 4(6)