References
- Watt JD, Throne DJ. Composition and pozzolanic properties of pulverised fuel ashes. II. Pozzolanic properties of fly ashes, as determined by crushing strength tests on lime mortars. J Appl Chem 1965; 15:595–604.
- Watt JD, Throne DJ. The composition and pozzolanic properties of pulverised fuel ashes. J Appl Chem 1966; 16:33–39.
- Saraswathy V, Muralidharan S, Thangavel K, Srinivasan S Cement Concr Res 2003; 25:673–680.
- Gopalakrishnan M, Sureshkumar P, Kanagarajan V, Thanusu J, Govindaraju R. A simplified green chemistry approaches to organic synthesis in solid media. Activated fly ash, an industrial waste (pollutant) as an efficient and novel catalyst for some selected organic reactions in solvent-free conditions under microwave irradiation. Arkivoc 2006; 13:130–141.
- Gopalakrishnan M, Thanusu J, Kanagarajan V. Easy-to-execute one-pot synthesis of 1,2,4,5-tetrazines catalyzed by activated fly ash. J Korean Chem Soc 2007; 51:520–525.
- Khatri C, Rani A. Synthesis of nanocrystalline solid acid catalyst from fly ash and their catalytic performance. Fuel 2008; 87:2886–2892.
- Narkhede HP, More UB, Dalal DS, Pawar NS, More DH, Mahulikar PP. Fly ash supported synthesis of 2-mercaptobenzothiazole derivatives under microwave irradiation. Synth Commun 2007; 37:573–577.
- Narkhede HP, More UB, Dalal DS, Mahulikar PP. Solid supported synthesis of bio-active carvacrol compounds using microwaves. Synth Commun 2008; 38:2413–2418.
- Gopalakrishnan M, Thanusu J, Kanagarajan V. A simple and efficient grindstone chemistry solid-state reaction procedure for the synthesis of heterocyclic oximes in dry media. J Korean Chem Soc 2008; 52:523–529.
- Kanagarajan V, Thanusu J, Gopalakrishnan M. Three component one-pot synthesis of novel pyrimidino thiazolidin-4-ones catalyzed by activated fly ash. Green Chem Lett Rev 2009; 2:161–167.
- Grimmett MR, In Comprehensive Heterocyclic Chemistry, Katritzky AR, Rees CW, Scriven EFV, Eds, Pergamon: Oxford, 1996, 3, pp 77–220.
- Greenhill JV, Lue L, In Progress in Medicinal Chemistry, Ellis GP, Luscombe DK, Eds, Elsevier: New York, 1993, Vol. 3.
- Jones RCF, Nichols JR. Thiamine coenzyme models: Imidazolinium ylides and the reactions of 2-(hydroxyalkyl)imidazolidines. Tetrahedron Lett 1990; 31:1771.
- Hayashi T, Kishi E, Soloshonok VA, Uozumi Y. Erthro-Selective aldol-type reaction of N-sulfonylaldimines with methyl isocyanoacetate catalyzed by gold(I). Tetrahedron Lett 1996; 37:4969.
- Jonesv RCF, Turner I, Howard KJ. A new route to homochiral piperidines Tetrahedron Lett 1993; 34:6329–6332.
- Isober T, Fukuda K, Araki Y, Ishikawa T. Modified guanidines as chiral superbases: The first example of asymmetric silylation of secondary alcohols. Chem Commun 2001; 3:243–244.
- Boland NA, Casey M, Hynes SJ, Matthews JW, Muller-Bunz H, Wilkes P. Preparation of enantiopure biimidazoline ligands and their use in asymmetric catalysis. Org Biomol Chem 2004; 2:1995–2002.
- Macinnes N, Duty S. Locomotor effects of imidazoline I2-site-specific ligands and monoamine oxidase inhibitors in rats with a unilateral 6-hydroxydopamine lesion of the nigrostriatal pathway. Br J Pharmacol 2004; 143:952–959.
- Dahlström M, Lindgren F, Berntsson K, Sjögren M, Mårtensson LG, Jonsson PR, Elwing H. Evidence for different pharmacological targets for imidazoline compounds inhibiting settlement of the barnacle Balanus improvisus. J Exp Zoolog Part A Comp Exp Biol 2005; 303:551–562.
- Zavala JA, Pereira ER, Zétola VH, Teive HA, Nóvak EM, Werneck LC. Hemorrhagic stroke after naphazoline exposition: case report. Arq Neuropsiquiatr 2004; 62:889–891.
- Silverman RM. The Organic Chemistry of Drug Design and Drug Action, Academic Press; New York, 1992, pp. 336 and 378.
- Martin KJ, Chen SF, Clark GM, Degen D, Wajima M, Von Hoff DD, Kaddurah-Daouk R. Evaluation of creatine analogues as a new class of anticancer agents using freshly explanted human tumor cells. J Natl Cancer Inst 1994; 86:608–613.
- Balasubramanian M; D’souza A. Studies on the reduction of some substituted cyclohexenones. Tetrahedron 1968; 24:5399–5408.
- Gopalakrishnan M, Sureshkumar P, Thanusu J, Kanagarajan V, Govindaraju R, Ezhilarasi MR. Microwave-promoted facile and rapid solvent-free procedure for the efficient synthesis of 3,4-dihydropyrimidin-2(1H)-ones and – thiones using ZrO2/SO42- as a reusable heterogeneous catalyst. Lett Org Chem 2006; 6:484–488.
- Gopalakrishnan M, Sureshkumar P, Thanusu J, Kanagarajan V. Synthesis, spectral analysis, antibacterial and antifungal activities of some 4,6-diaryl-4,5-dihydro-3-hydroxy-2[H]-indazole-a novel fused indazole derivative. J Enzyme Inhib Med Chem 2008; 23:974–979.
- Gopalakrishnan M, Sureshkumar P, Thanusu J, Kanagarajan V. Design, synthesis, characterization, antibacterial and antifungal activities of a novel class of 5,7-diaryl-4,4-dimethyl-4,5,6,7-tetrahydropyridino[3,4-d]-1,2,3-selenadiazoles. J Enzyme Inhib Med Chem 2008; 23:347–351.
- Nielson AT, Houlihan WJ. The aldol condensation. Org React 1968; 16:1–438.
- Dhar ML, Dhar MM, Dhawan BN, Mehrotra BN, Ray C. Screening of Indian plants for biological activity: I. Indian J Exp Biol 1968; 6:232–247.
- Neef G, Eder U, Sauté G. One step conversion of esters to 2-imidazolidines and benzimdazolines. J Org Chem 1981; 46:2824–2826.
- George B, Papadopoulos EP Heterocycles from N-ethoxycarbonylthioamides and dinucleophilic agents. J Org Chem 1977; 42:441–443.
- Fujioka H, Murai K, Ohab Y, Hiramatsu A, Kita Y. A mild and efficient one-pot synthesis of 2-dihydroimidazoles from aldehydes. Tetrahedron Lett 2005; 46:2197–2199.
- Peddibhotla S, Tepe JJ. Multicomponent synthesis of highly substituted imidazolines via a silicon mediated 1,3-dipolar cycloaddition. Synthesis 2003; 9:1433–1440.
- Huh DH, Ryu H, Kim YG. A novel synthetic method for 2-arylmethyl substituted imidazolidines and imidazoles from 2-aryl-1,1-dibromoethenes. Tetrahedron 2004; 60:9857–9862.
- Mitchell JM, Finney NS. An efficient method for the preparation of N,N-disubstituted 1,2-diamines. Tetrahedron Lett 2000; 41:8431–8434.
- You SL, Kelly JW. Highly efficient enantiospecific synthesis of imidazoline-containing amino acids using bis(triphenyl)oxodiphosphonium trifluoromethanesulfonate. Org Lett 2004; 6:1681–1683.