[1]
Schutz, H. Benzodiazepines; Springer: Heidelberg, 1982.
[2]
Landquist, J.K.; Katritzky, A.R.; Rees, C.W. Pergamon In: Comprehensive Heterocyclic Chemistry; Oxford, 1984; pp. 166-170.
[3]
Makaron, L.; Moran, C.A.; Namjoshi, O.; Rallapalli, S.; Cook, J.M.; Rowlett, J.K. Cognition-impairing effects of benzodiazepine-type drugs: Role of GABAA receptor subtypes in an executive function task in rhesus monkeys. Pharmacol. Biochem. Beh., 2013, 104, 62-68.
[4]
Allison, C.; Pratt, J.A. Neuroadaptive processes in GABAergic and glutamatergic systems in benzodiazepine dependence. Pharmacol. Therapeut., 2003, 98, 171-195.
[5]
Hawkins, E.J.; Malte, C.A. Prevalence and trends of benzodiazepine use among Veterans Affairs patients with posttraumatic stress disorder. Drug Alcohol Depend., 2012, 124, 154-161.
[6]
Banerji, A.; Goomer, N. A new synthesis of flavones. Synthesis, 1980, 11, 874-875.
[7]
Havsteen, B. Flavonoids, a class of natural products of high pharmacological potency. Biochem. Pharmacol., 1983, 32, 1141-1148.
[8]
Cortés, E.; María, A.; Sanabria, H.; García, O. Synthesis and Spectral Properties of 11- [(o -; and p -substituted) is the clozapine that is an atypical antipsychotic agent with. J. Heterocyclic. Chem., 2002, 39, 55-57.
[9]
Wang, S-L.; Cheng, C.; Wu, F-Y.; Jiang, B.; Shi, F.; Tu, S-J.; Rajale, T.; Li, G. Microwave-assisted multicomponent reaction in water leading to highly regioselective formation of benzo[f]azulen-1-ones. Tetrahedron, 2011, 67, 4485-4493.
[10]
Kaoua, R.; Nedjar-Kolli, B.; Roisnel, T.; Le Gal, Y.; Lorcy, D. Electroactive 1,5-benzodiazepines bearing either a tetrathiafulvalene or a ferrocene moiety. Tetrahedron, 2013, 69, 4636-4640.
[11]
Tonkikh, N.N.; Strakovs, A. 11-Aryl-3,3-dimethyl-7- and 7,8-Substituted 1, 2,3,4,10,11-Hexahydro-5H-dibenzo[b,e]-1,4-diazepin-1-ones. Chem. Hetero. Compd., 2004, 40, 7-8.
[12]
Tolpygin, I.E.; Mikhailenko, N.V. 11-R-dibenzo[b,e][1,4]diazepin-1-ones, the chemosensors for transition metal cations. Russ. J. Gen. Chem., 2012, 82, 1141-1147.
[13]
Sangshetti, J.N.; Chouthe, R.S. Green synthesis and anxiolytic activity of some new dibenz-[1,4] diazepine-1-one analogues. Arabian. J. Chem., 2013, 7, 415-419.
[14]
Cortes, C.A.; Valencia, A.L. New derivatives of dibenzo[b,e][1,4]dia-zepin‐1‐ones by an efficient synthesis and spectroscopy. J. Heterocycl. Chem., 2007, 44, 183-184.
[15]
Naeimi, H.; Moradian, M. Copper (I) -N2 S2 -salen type complex covalently anchored onto MCM-41 silica: An efficient and reusable catalyst for the A 3 -coupling reaction toward propargylamines. Appl. Organometal. Chem., 2013, 27, 300-306.
[16]
Naeimi, H.; Nejadshafiee, V. Efficient one-pot click synthesis of β-hydroxy-1,2,3-triazoles catalyzed by copper(i)@phosphorated SiO2via multicom-ponent reaction in aqueous media. New J. Chem., 2014, 38, 5429-5435.
[17]
Naeimi, H.; Nejadshafiee, V.; Masoum, S. Copper@PMO nanocomposites as a novel reusable heterogeneous catalyst for microwave-assisted green synthesis of β-hydroxy-1,2,3-triazoles through experimental design protocol. Appl. Organomet. Chem., 2015, 25, 314-321.
[18]
Naeimi, H.; Nejadshafiee, V.; Masoum, S. Highly efficient copper-imprinted functionalized mesoporous organosilica nanocomposites as a recyclable catalyst for click synthesis of 1,2,3-triazole derivatives under ultrasound irradiation: multivariate study by factorial design of experiments. RSC Adv, 2015, 5, 15006-15016.
[19]
Yang, X.; Chen, D.; Liao, S.; Song, H.; Li, Y.; Fu, Z.; Su, Y. High-performance Pd–Au bimetallic catalyst with mesoporous silica nanoparticles as support and its catalysis of cinnamaldehyde hydrogenation. J. Catal., 2012, 291, 36-43.
[20]
Yang, H.; Wang, Y.; Qin, Y.; Chong, Y.; Yang, Q.; Li, G.; Zhang, L.; Li, W. One-pot preparation of magnetic N-heterocyclic carbene-functionalized silica nanoparticles for the Suzuki–Miyaura coupling of aryl chlorides: improved activity and facile catalyst recovery. Green Chem., 2011, 13, 1352-1361.
[21]
Lee, Y-Y.; Wu, K.C-W. Conversion and kinetics study of fructose-to-5-hydroxymethylfurfural (HMF) using sulfonic and ionic liquid groups bi-functionalized mesoporous silica nanoparticles as recyclable solid catalysts in DMSO systems. Phys. Chem. Chem. Phys., 2012, 14, 13914-13917.
[22]
He, W.; Zhang, F.; Li, H. Active and reusable Pd(ii) organometallic catalyst covalently bonded to mesoporous silica nanospheres for water-medium organic reactions. Chem. Sci., 2011, 2, 961-966.
[23]
Gu, Y.; Ogawa, C.; Kobayashi, J.; Mori, Y.; Kobayashi, S. A heterogeneous silica‐supported scandium/ionic liquid catalyst system for organic reactions in water. Angew. Chem. Int. Ed., 2006, 118, 7375.
[24]
Magna, L.; Morvan, D. Ionic liquids and catalysis : Recent progress from knowledge to applications. Appl. Catal. A., 2010, 373, 1-56.
[25]
Ma, Z.; Yu, J.; Dai, S. Preparation of inorganic materials using ionic liquids. Adv. Mater., 2010, 22, 261-285.
[26]
Chen, Z.; Greaves, T.L.; Caruso, R.A.; Drummond, C.J. Long-range ordered lyotropic liquid crystals in intermediate-range ordered protic ionic liquid used as templates for hierarchically porous silica. J. Mater. Chem., 2012, 22, 10069-10076.
[27]
Sangsuwan, R.; Sangher, S.; Aree, T.; Mahidol, C. XRuchirawatab, S.; Kittakoop, P. An organocatalyst from renewable materials for the synthesis of coumarins and chromenes: three-component reaction and multigram scale synthesis. RSC Adv, 2014, 4, 13708-13718.
[28]
Miao, W.; Chan, T.H. Ionic-Liquid-Supported Organocatalyst: Efficient and Recyclable Ionic-Liquid-Anchored Proline for Asymmetric Aldol Reaction. Adv. Synth. Catal., 2006, 348, 1711-1718.
[29]
Tu, S-J.; Zhang, X-H.; Han, Z-G.; Cao, X-D.; Wu, S-S.; Yan, S.; Hao, W-J.; Ma, N. Synthesis of isoxazolo[5,4-b]pyridines by microwave-assisted multi-component reactions in water. J. Comb. Chem., 2009, 11, 428-432.
[30]
Jiang, B.; Li, C.; Shi, F.; Tu, S-J.; Kaur, P.; Wever, W.; Li, G. Four-component domino reaction providing an easy access to multifunctionalized tricyclo[6.2.2.0(1,6)]dodecane derivatives. J. Org. Chem., 2010, 75, 2962-2965.
[31]
Ma, N.; Jiang, B.; Zhang, G.; Tu, S-J.; Wever, W.; Li, G. New multicomponent domino reactions (MDRs) in water: highly chemo-, regio- and stereoselective synthesis of spiro[1,3]dioxanopyridine-4,6-diones and pyrazolo[3,4-b]pyridines. Green Chem., 2010, 12, 1357-1361.
[32]
Jiang, B.; Tu, S-J.; Kaur, P.; Wever, W.; Li, G. Four-Component Domino Reaction Leading to Multifunctionalized. J. Am. Chem. Soc., 2009, 131, 11660-11661.
[33]
Naeimi, H.; Nejadshafiee, V.; Islami, M.R. Iron (III)-doped, ionic liquid matrix-immobilized, mesoporous silica nanoparticles: Application as recyclable catalyst for synthesis of pyrimidines in water. Micropor. Mesopor. Mate., 2016, 227, 23-30.
[34]
Leofanti, G.; Padovan, M.; Tozzola, G.; Venturelli, B. Surface area and pore texture of catalysts. Catal. Today, 1998, 41, 207-219.