[3]
Gautam, N.; Chourasia, O.P. Synthesis, characterization, antimicrobial, insecticidal and anthelmintic screening of some new s-triazine derivatives of pyrazoline, pyrimidine, isoxazoline and isothiazoline moiety. Indian J. Chem., 2012, 51b, 1400-1410.
[6]
Karthikeyan, P.; Kumar, S.S.; Jagadeesh, R.V.; Bhagat, P.R. Solvent-free synthesis of substituted-2-pyrazolines using imidazolium based ionic liquid as a solvent and catalyst: A green route approach. Asian J. Chem., 2012, 24, 1351-1353.
[8]
Sharma, S.; Sharma, A. Solvent-free synthesis of new-1-acetyl-3-(4-fluoronaphthyl)-5-substituted aryl pyrazolines as spermicides. J. Indian Chem. Soc., 2008, 85, 750-753.
[11]
Rao, J.N.; Sujith, K.V.; Kalluraya, B. An efficient microwave assisted synthesis of some pyrazolines and their biological activity. Indian J. Heterocycl. Chem., 2009, 18, 365-368.
[18]
Lancaster, M. Green Chemistry: An Introductory Text, 3rd ed; Royal Society of Chemistry: Cambridge, 2016.
[19]
Matlack, A.S. Introduction to Green Chemistry, 2nd ed; CRC Press: New York, 2001.
[21]
Lancaster, M. Handbook of Green Chemistry and Technology, 2nd ed; John Wiley and Sons: New York, 2002.
[26]
Anastas, P.T.; Warner, J.C. Green Chemistry: Theory and Practice, Ist ed; Oxford: New York, 1998.
[29]
Toda, F.; Takumi, H.; Yamaguchi, H. Grignard reactions in the solid state. Chem. Expr., 1989, 4, 507-510.
[30]
Desiraju, G.R. Organic Solid State Chemistry, Ist ed; Elsevier Science Publishers: New York, 1987.
[44]
Murray, R.D.H. The Natural occurring Coumarins: Progress in the Chemistry of Organic Natural Products, Ist ed; Springer: New York, 2002.
[45]
Kennedy, R.O.; Tharnes, R.D. Coumarins: Biology, Application and Mode of Action, 2nd ed; John Wiley and sons: New york, 1997.
[46]
Zahradink, M. The Production and Application of Fluorescent Brightening Agents; Wiley, 1992.
[48]
Knochel, P.; Molander, G.A. Comprehensive Organic Synthesis.Elsevier, (2nd ed); , 2014.
[51]
Maleki, A.; Ravaghi, P.; Movahed, H.; Aghaie, M. New multicomponent approach for the synthesis of coumarin derivatives by using environmentalfriendly core/shell nanocatalyst. The 20th International Electronic Conference on Synthetic Organic Chemistry, 2016, 51B
[52]
Rosen, T. The perkin reaction: In comprehensive organic synthesis. Elsevier Science B.V. Amsterdum, 1991, vol. 2, 395-408.
[60]
Witte, E.C.; Neubert, P.; Roesch, A. Ger. Offen. Patent DE3427985, 1986.
[62]
El-Saghier, A.M.M.; Naili, M.B.; Rammash, B.K.; Saleh, N.A.; Kreddan, K.M. Synthesis and antibacterial activity of some new fused chromenes. ARKIVOC, 2007, 16, 83-91.
[77]
Gunnlaugsson, T.; Nieuwenhuyzen, M.; Richard, L.; Thoss, V. Novel sodium-selective fluorescent PET and optically based chemosensors: towards Na+ determination in serum. J. Chem. Soc. Perkin Trans., 2002, 2, 141-150.
[88]
Bhargava, S.; Rajwanshi, L.K. Synthesis of some novel pyrido [2, 3-d]pyrimidine derivatives and their antimicrobial investigation. Indian J. Chem., 2013, 52B, 448-452.
[95]
Archana; Srivastava, V.K.; Chandra, R.; Kumar, A. Synthesis of potential quinazolinonyl pyrazolinesand quinazolinyl isoxazolines as anticonvulsant agents. Indian J. Chem., 2002, 41B, 2371-2375.
[115]
Freeman, H.S.; Peters, A.T. Colorants for Non-Textile Applications, 1st ed.; Elsevier Science B.V: Amsterdum, 2000.
[121]
Tatsuta, M.; Kitao, T. Reagent for detecting and diagnosing cancer. Publication No. JP01–207247 A, 1989.
[122]
Aszalos, A.; Weaver, J.L.; Pine, P.S. Methods of usingazo dyes and their derivatives. US Patent 5 5,468,469. 1995.
[128]
Berlin, K.D.; Herd, M.D. Novel 2-amino-4-aryl-substituted and 2-amino-4,5-disubstituted-thiazoles. Proc. Okla. Acad. Sci., 1991, 71, 29-33.
[129]
Sharma, P.K.; Swonhney, S.N.; Gupta, A.; Singh, G.B.; Bani, S. Synthesis of some novel 2,4-disubstituted thiazoles. Indian J. Chem., 1998, 37B, 371-375.
[149]
Bose, D.S.; Narsaiah, A.V. An efficient benzyltriethylammonium chloride catalyzed preparation of electrophilic alkenes: A practical synthesis of trimethoprim. J. Chem. Res., 2001, 2001(1), 36-38.
[163]
Kadish, K.M.; Smith, K.M.; Guilard, R. Handbook of Porphyrin Science, With
Applications to Chemistry, Physics, Materials Science, Engineering, Biology
and Medicine, Ed; World Scientific Publishing, Singapore, 2010.
[173]
Toja, E.G.C.; Barzaghi, F.; Galliani, G.U.S. Chem. Abstr. U.S. Patent 4, 885, 307. 1989.
[174]
Paal, C. Synthese von thiophen- und pyrrolderivaten. berichte der deutschen chemischen desellschaft. ber. dtsch. Chem. Ges., 1885, 18, 367-371. (b) Knorr, L. Einwirkung des diacetbernsteinsäureesters auf ammoniak und primäre aminbasen. berichte der deutschen chemischen gesellschaft. ber. dtsch. Chem. Ges., 1885, 18, 299-311.
[186]
Diederich, F.; Stang, P.J. Metal Catalysed Cross Coupling Reactions; Wiley-VCH: Weinheim, Germany, 1988.
[189]
Sovak, M. Radiocontrast agents. In: Handbook of Experimental Pharmacology; Springer: Berlin, 1984.
[191]
(a) Heindel, N.D.; Burnes, H.D.; Honds, T.; Brandy, L.W. Chemistry of Radiopharmaceuticals; Masson: New York, 1997.
(b) Nicolaou, K.C. The battle of calicheamic- in1. Angew. Chem. Int. Ed. Engl., 1993, 32, 1377.
[221]
Kini, S.G.; Bhat, A.R.; Bhat, R.; Narayanaswamy, N. Synthesis and antimicrobial activity of new 3,5-disubstituted isoxazoles. Indian J. Heterocycl. Chem., 2008, 17, 319-322.
[227]
Solankee, A.; Patel, J. Synthesis of chalcones, pyrazolines, aminopyrimidines and pyrimidine thiones as anti-bacterial agents. Indian J. Chem., 2004, 1580-1584.
[228]
Bapna, A.; Ojha, S.; Talesara, G.L. Facile synthesis of alkoxy phthalimide derivatized benzimidazole assembled pyrazoles, pyrimidines and isoxazoles, via common intermediate chalcone. Indian J. Chem., 2008, 1096-1107.
[240]
Fan, W.Q.; Katritzky, A.R. Comprehensive Heterocyclic Chemistry II., 1996, vol. 4, 1-126.
[242]
Sridar, V. Rate acceleration of fischer-indole cyclization by microwave irradiation. Indian J. Chem., 1997, 36B, 86-87.
[244]
Landge, S.M.; Schmidt, A.; Outerbridge, V.; Török, B. Synthesis of pyrazoles by a one-pot tandem cyclization-dehydrogenation approach on Pd/C/K-10 catalyst. Synlett, 2007, 10, 1600-1604.
[250]
Oussaid, A.; Loupy, A. Selective oxidation of arenes in dry media under
focused microwaves. J. Chem. Res. (S)., 1997, (9), 342-343.
[258]
Verma, R.S.; Saini, R.K.; Dalip, K. An expeditious synthesis of flavones on montmorillonite k-10 clay with microwaves. J.Chem.Res. (S)., 1998, 348-349.
[278]
Chu, N.Y.C. 4n+2 systems: Spirooxazines. In: Photochromism: molecules and systems; Elsevier: Amsterdam, 1990; pp. 493-508.
[280]
Maeda, S. Spirooxazines. In: organic photochromic and thermochromic compounds; Crano, J.C.; Guglielmetti, R., Eds.; Plenum Press: New York, 1999; Vol. 1, Ch. 2, pp. 86-109.
[287]
Karmee, S.K. Application of microwave irradiation in biocatalysis. Res. J. Biotechnol., 2006, 1, 1.
[292]
Atsushi, Y.; Yoshizawa-Fujita, M.; Yuko, T.; Masahiro, R. In Microwave-assisted enzymatic polymerization of PLG Acopolymers and hybridization with hydroxyapatite. 238th ACS National Meeting, Washington, DC2009.
[300]
Gupta, R.; Gupta, N.; Jain, A. Improved synthesis of chalcones and pyrazolines under ultrasonic irradiation. Indian J. Chem., 2010, 49B, 351-355.
[306]
Kaur, B.; Parmar, A.; Kumar, H. Manganese perchlorate catalyzed efficient greener sonochemical synthesis of aryl-14-h-dibenzo [a, j] xanthenes and 4-substituted 2Hchromen-2-ones. Heterocycl. Lett., 2011, 1, 213-219.