1. O. Elhady, E. Mansour, M. Elwassimy, S. Zawam, A. Drar, S. A. Raheem, (2022) Selective synthesis, characterization, and toxicological activity screening of some furan compounds as pesticidal agents, Curr. Chem. Lett., 11 (3), 285-290.
2. M.S. Tolba, M. Sayed, A.M. Kamal El-dean, R. Hassanien, S.A. Abdel-Raheem, M. Ahmed, (2021) Design, synthesis and antimicrobial screening of some new thienopyrimidines, Org. Commun., 14(4), 334-345.
3. S.A.A. Abdel-Raheema, A.M.K. El-Deanb, M.A. Abdul-Malikc, R. Hassaniend, M.E.A. El-Sayeda, A.A. Abd-Ellae, S.A. Zawamf, M.S. Tolba, (2022) Synthesis of new distyrylpyridine analogs bearing amide substructure as effective insecticidal agents, Curr. Chem. Lett., 11 (1), 23-28.
4. S.A.A. Raheem, A.M. Kamal, E. Dean, R. Hassanien, M.E.A. El-Sayed, A.A. Abd-Ella, (2021) Synthesis and characterization of some distyryl-derivatives for agricultural uses, Eur. Chem. Bull., 10(1): 35-38.
5. M.S. Tolba, A.M. Kamal El-Dean, M. Ahmed, R. Hassanien, M.S.R. Melad, S.K. Mohamed, S.A. Zawam, S.A.A. Abdel-Raheem, (2022) Synthesis, reactions, and applications of pyrimidine derivatives, Curr. Chem. Lett., 11(1), 121-138.
6. M.S. Tolba, M.A.A. Ul-Malik, A.M.K. El-Dean, A.A. Geies, S.M. Radwan, R.M. Zaki, M. Sayed, S.K. Mohamed, S.A.A. Abdel-Raheem, (2021) An overview on synthesis and reactions of coumarin-based compounds, Curr. Chem. Lett., 11(1), 29-42.
7. A.A. Abd-Ella, S.A. Metwally, M.A. Abdul-Malik, Y.A. El-Ossaily, F.M. Abd Elrazek, S.A. Aref, Y.A. Naffea, (2022) A review on recent advances for the synthesis of bioactive pyrazolinone and pyrazolidinedione derivatives, Curr. Chem. Lett., 11(2), 157-172.
8. S.A.A. Abdel-Raheem, A.M.K. El‐Dean, M.A. Abdul-Malik, A.A. Abd-Ella, E. Altaifi, R. Hassanien, M.E.A. Elsayed, S.K. Mohamed, S.A. Zawam, Y.A. Naffea, E. Bakhite,
S.A.A. Abdel-Raheem, (2022) A concise review on some synthetic routes and applications of pyridine scaffold compounds, Curr. Chem. Lett., 10(4), 337-362.
9. A. Abdelhamid, A. Elsaghiera, S. Aref, M. Gad, N. Ahmed, S. Abdel-Raheem, (2022) Preparation and biological activity evaluation of some benzoyl thiourea and benzoylurea compounds, Curr. Chem. Lett., 10(4), 371-376.
10. M.A. Gad, S.A. Aref, A.A. Abdelhamid, M.M. Elwassimy, S.A.A. Abdel-Raheem, (2021) Biologically active organic compounds as insect growth regulators (IGRs): introduction, mode of action, and some synthetic methods, Curr. Chem. Lett., 10 (4) 393-412.
11. R.M. Ghalib, S.H. Mehdi, A.M. Malla, G.A. Bogdanović, (2020) Synthesis of new seven-member heterocyclic rings: An easy access to Indeno-benzo[1,4]diazepines, Arabian Journal of Chemistry, 13(10), 7338-7345.
12. M.A. Rashid, A. Ashraf, S.S. Rehman, S.A. Shahid, A. Mahmood, M. Faruq, (2019) 1,4-Diazepines: A Review on Synthesis, Reactions and Biological Significance, Current Organic Chemistry, 16(5), 709-729.
13. M.E. Haimer, M. Palkó, M. Haukka, M. Gajdács, I. Zupkó, F. Fülöp, (2021) Synthesis and biological evaluation of the new ring system benzo[f]pyrimido[1,2-d][1,2,3]triazolo[1,5-a][1,4]diazepine and its cycloalkane and cycloalkene condensed analogs, RSC Advances, 11(12), 6952-6957.
14. M.A. Rashid, A. Ashraf, S.S. Rehman, S.A. Shahid, A. Mahmood, M. Faruq, (2019) 1,4-Diazepines: A Review on Synthesis, Reactions and Biological Significance, Curr Org Synth., 16(5),709-729.
15. Y. Malki, L.T. Maillard, N. Masurier, (2021) 1,3-Diazepine Derivatives: Strategies for Synthesis, Eur. J. Org. Chem.., https://doi.org/10.1002/ejoc.202100492
16. F. Křemen, M. Gazvoda, S. Kafka, K. Proisl, A. Srholcová, A. Klásek, Damijana Urankar, and Janez Kosmrlj (2017) Synthesis of 1,4-Benzodiazepine-2,5-diones by Base Promoted Ring Expansion of 3-Aminoquinoline-2,4-diones, J. Org. Chem., 82, 1, 715–722.
17. M.P. Sadashiva, Basappa, N. Swamy, F. Li, K.A. Manu, M. Sengottuvelan, D.S. Prasanna, N.C. Anilkumar, G. Sethi, K. Sugahara, K.S. Rangappa. (2012) Anti-cancer activity of novel dibenzo[b,f]azepine tethered isoxazoline derivatives. BMC Chem Biol., 12(5), 1-11.
18. E Esposito , S Cuzzocrea, New therapeutic strategy for Parkinson's and Alzheimer's disease, Curr Med Chem., 17(25), 2764-2774.
19. Tawfik A. Khattab, Mohamed Rehan, (2018) A Review on Synthesis of Nitrogen-Containing Heterocyclic Dyes for Textile Fibers - Part 2: Fused Heterocycles, Egyptian Journal of Chemistry, 61(6), 989-1018.
20. A. Shafie, M.M. Khanaposhtani, M. Asadi, N. Rahimi, P. R. Ranjbar, J.B. Ghasemi, B. Larijani, M. Mahdavi, H. Shafaroodi, A.R. Dehpour, (2020) Novel fused 1,2,3-triazolo-benzodiazepine derivatives as potent anticonvulsant agents: design, synthesis, in vivo, and in silico evaluations, Mol Divers, 24(1), 179-189.
21. A. Chimirri, S. Grasso, R. Ottanà, G. Romeo, M. Zappala, (1990) Synthesis and stereochemistry of novel [1,2,4]oxadiazolo[4,5-a][1,5]benzodiazepine derivatives, Journal of Heterocyclic Chemistry, 27(2), 371-374.
22. P. Kralova, M. Malon, M. Soural, (2017) Stereoselective Synthesis of Benzo[e][1,4]oxazino[4,3-a][1,4]diazepine-6,12-diones with Two Diversity Positions, ACS Comb. Sci., 19(12), 770–774.
23. G. Varvounis, (2016) An Update on the Synthesis of Pyrrolo[1,4]benzodiazepines, Molecules, 21(2), 154-210.
24. M.A. Rashid, A.Ashraf, S.S. Rehman, S.A. Shahid, A. Mahmood, M. Faruq, (2019)1,4-Diazepines: A Review on Synthesis, Reactions and Biological Significance, Curr Org Synth, 16(5), 709-729.
25. Nicholas E. Calcaterra, James C. Barrow, (2014) Classics in Chemical Neuroscience: Diazepam (Valium), ACS Chem Neurosci., 5(4), 253–260.
26. Dong Jin Lee, Hong Sik Han, Jinhwan Shin, and Eun Jeong Yoo, (2014) Multicomponent [5 + 2] Cycloaddition Reaction for the Synthesis of 1,4-Diazepines: Isolation and Reactivity of Azomethine Ylides, J. Am. Chem. Soc., 136(33), 11606–11609.
27. Chang Guo, Basudev Sahoo, Constantin G. Daniliuc, and Frank Glorius, (2014) N-Heterocyclic Carbene Catalyzed Switchable Reactions of Enals with Azoalkenes: Formal [4 + 3] and [4 + 1] Annulations for the Synthesis of 1,2-Diazepines and Pyrazoles, J. Am. Chem. Soc., 136(50), 17402–17405.
28. S. Tao, Q. Bu, Q. Shi, D. Wei, B. Dai, N. Liu, (2020) Synthesis of Benzodiazepines Through Ring Opening/Ring Closure of Benzimidazole Salts, Chemistry – A European Journal, 26,(15), 3252-3258.
29. M.J. Plunkett, J.A. Ellman, (1995) Solid-Phase Synthesis of Structurally Diverse 1,4-Benzodiazepine Derivatives Using the Stille Coupling Reaction, J. Am. Chem. Soc., 117(11), 3306–3307.
30. I.R. Siddiqui, S. Shamim, D. Kumar, Shireena, M.A. Waseema, (2012) Tandem imino-pinacol coupling-aza-Michael reaction promoted by Zn/InCl3: a novel multicomponent strategy for diastereoselective synthesis of monocyclic 1,4-diazepine in water, New J. Chem., 36(11), 2209-2214.
31. M.A. Ghasemzadeh, N.G. Seresht, (2015) Facile and efficient synthesis of benzo[b][1,5]diazepines by three-component coupling of aromatic diamines, Meldrum’s acid, and isocyanides catalyzed by Fe3O4 nanoparticles, Research on Chemical Intermediates, 41(11), 8625–8636.
32. D.V. Jarikote, S. Siddiqui, R Rajagopal, T. Daniel, R. J Lahoti, K. V Srinivasan, (2003) Room Temperature Ionic Liquid Promoted Synthesis of 1,5-Benzodiazepine Derivatives under Ambient Conditions, ChemInform, 44(9), 1835-1838.
33. D. Shobha, M.A. Chari, M. Khagga, K.H. Ahn, (2009) Silica gel-supported sulfuric acid-catalyzed synthesis of 1,5-benzodiazepine derivatives, Journal of Heterocyclic Chemistry, 46(5), 1028 - 1033.
34. S. De, R. Gibbs, (2005) Scandium(III) Triflate as an Efficient and Reusable Catalyst for Synthesis of 1,5-Benzodiazepine Derivatives, Tetrahedron Letters, 46(11), 1811-1813.
35. M. Jeganathan, K. Pitchumani, (2014) Solvent-Free Syntheses of 1,5-Benzodiazepines Using HY Zeolite as a Green Solid Acid Catalyst, ACS Sustainable Chem. Eng., 2(5), 1169–1176.
36. S.V. Goswami, P.B. Thorat, S.R. Bhusare, (2013) Phenylboronic Acid Catalyzed Synthesis of 1,5-Benzodiazepines via Cyclocondensation of o-Phenylenediamine and Ketones, Journal of Chemical Sciences, 125(4), 745-749.
37. S. Vajiravelu, K. Deepa, M. Palanichamy, V. Murugesan, (2011) [(L)Proline]2Zn Catalysed Synthesis of 1,5‐Benzodiazepine Derivatives Under Solvent‐Free Condition, Synthetic Communications, 34(21), 3833-3846.
38. A. Kamal, E. Laxman, N. Laxman, N.V. Rao, (2000) Synthesis of pyrrolo[2,1-c[1,4]benzodiazepines via reductive cyclization of omega-azido carbonyl compounds by TMSI: an efficient preparation of antibiotic DC-81 and its dimers, Bioorg Med Chem Lett, 10(20), 2311-2313.
39. S.K. Mahato, C. Acharya, K.W. Wellington, P. Bhattacharjee, P. Jaisankar, (2020) InCl3: A Versatile Catalyst for Synthesizing a Broad Spectrum of Heterocycles, ACS Omega, 5(6), 2503–2519.
40. O.A. Shemyakina, O.G. Volostnykh, A.V. Stepanov, A.G. Mal’kina, I.A. Ushakov, K. Apartsin, V.V. Kireeva, B. Trofimov, (2018) DBU as a scaffold for the synthesis of [1,3]oxazolo[2’,3’:2,3]pyrimido-[1,2-a]azepines: annulation with aromatic cyanopropargylic alcohols, Mendeleev Communications, 28(2), 128-130.
41. J.S. Yadav, Y. Srivastava, (2020) An efficient microwave-assisted synthesis of some novel 1, 4 diazepine derivatives as possible antimicrobial agents, Rasayan Journal of Chemistry, 3(4),726-730.
42. S.K. Maury, D. Kumar, A. Kamal, H.K. Singh, S. Kumari, S. Singh, (2021) A facile and efficient multicomponent ultrasound-assisted "on water" synthesis of benzodiazepine ring, Mol Divers., 25(1), 131-142.
43. N. Kausar, P. Mukherjee, A.R. Das, (2016) Practical carbocatalysis by graphene oxide nanosheets in aqueous medium towards the synthesis of diversified dibenzo[1,4]diazepine scaffolds, RSC Adv., 91(6), 88904-88910
44. A.M. Berrada, D. Grondin, S. Bennicia, A. Auroux, (2012) Design of amphoteric mixed oxides of zinc and Group 3 elements (Al, Ga, In): migration effects on basic features, Phys. Chem. Chem. Phys.,14(12), 4155-4161.
45. B.V. Kumar, H.S.B. Naik, D.K. Girija, (2011) ZnO nanoparticle as catalyst for efficient green one-pot synthesis of coumarins through Knoevenagel condensation, Journal of Chemical Sciences, 123(5), 615-621.
46. B. Banerjee, (2017) Recent developments on nano-ZnO catalyzed synthesis of bioactive heterocycles, J Nanostruct Chem., 7, 389–413.
47. R. Tayebee, A.H Nasr, S. Rabiee, E. Adibi, (2013) Zinc Oxide as a Useful and Recyclable Catalyst for the One-Pot Synthesis of 2,4,6-Trisubstituted-1,3,5-trioxanes under Solvent-Free Conditions, Ind. Eng. Chem. Res., 52(28), 9538–9543.
48. H.C. Yao, (1964) Azohydrazone Conversion. II. The Coupling of Diazonium Ion with β-Diketones, J. Org. Chem., 29 (10), 2959–2963.
49. G.K. Reen, M. Ahuja, A. Kumar, R. Patidar, P. Sharma, (2017) ZnO Nanoparticle-Catalyzed Multicomponent Reaction for the Synthesis of 1,4-Diaryl Dihydropyridines, Organic Preparations, and Procedures International, 49(3), 273-286.
50. H. Sachdeva, R. Saroj, (2013) ZnO Nanoparticles as an Efficient, Heterogeneous, Reusable, and Ecofriendly Catalyst for Four-Component One-Pot Green Synthesis of Pyranopyrazole Derivatives in Water, Sci. World J., 1-8.
51. I. Khan, K. Saeed, I. Khan, (2019) Nanoparticles: Properties, applications and toxicities, Arab. J. Chem., 12, 908-931.
52. L. Zhengyi, Y. Zhaozhuo, L. Xiaoxiang, L. Chuanhui, W. Hongguo, Z. Wenfeng, L. Hu, Y. Song Ya, (2020) Recent advances in liquid hydrosilane-mediated catalytic N-formylation of amines with CO2, RSC Adv., 10, 33972-34005.
53. D. Geedkar, A. Kumar, K. Kumar, P. Sharma, (2021) Hydromagnesite sheets impregnated with cobalt–ferrite magnetic nanoparticles as heterogeneous catalytic system for the synthesis of imidazo[1,2- a ]pyridine scaffolds, RSC Advances, 11(38), 23207-23220.
54. D. Geedkar, A. Kumar, P. Sharma, (2020) Multiwalled carbon nanotubes crowned with nickel‐ferrite magnetic nanoparticles assisted heterogeneous catalytic strategy for the synthesis of benzo[d]imidazo[2,1‐b]thiazole scaffolds, Journal of Heterocyclic Chemistry, 57(12), 4331-4347.
55. D. Geedkar, A. Kumar, G.K. Reen, P. Sharma, (2020) Titania‐silica nanoparticles ensemblies assisted heterogeneous catalytic strategy for the synthesis of pharmacologically significant 2,3‐diaryl‐3,4‐dihydroimidazo[4,5‐b]indole scaffolds, Journal of Heterocyclic Chemistry, 57(4), 1963-1973.
56. D. Geedkar, A. Kumar, G.K. Reen, P. Sharma, (2022) Molecular Iodine-Catalyzed Synthesis of Imidazo[1,2 a]Pyridines: Screening of Their In Silico Selectivity, Binding Affinity to Biological Targets, and Density Functional Theory Studies Insight, ACS Omega, 7, 22421-22439.