[1]   A. K. Mukerjee and R. Ashare, “Isothiocyanates in the Chemistry of Heterocycles,” Chemical Review, Vol. 91, No. 1, 1991, pp. 1-24. doi:10.1021/cr00001a001

[2]   S. I. El-Desoky, H. A. Etman, S. B. Bondock, A. A. Fadda and M. A. Metwally, “Utility of Isothiocyanates in Heterocyclic Synthesis,” Sulfur Letter, Vol. 25, No. 5, 2002, pp. 199-205. doi:10.1080/02786110214496

[3]   S. I. El-Desoky, S. B. Bondock, H. A. Etman, A. A. Fadda and M. A. Metwally, “Synthesis of Some New Thiazole Derivatives of Pharmaceutical Interest,” Sulfur Letter, Vol. 26, No. 3, 2003, pp. 127-135. doi:10.1080/0278611031000095331

[4]   K. N. Zelenin, O. V. Solod, V. V. Alekseev, T. I. Pekhk, O. B. Kuznetsova, P. B. Terent’ev and A. G. Kalandarishvili, “Synthesis of Pyrazole, 1,3,4-Thiadiazole, and 1,2,4-Triazole Derivatives by Condensatoin of 1,3-Dioxo Compounds with Thiosemicarbazide Derivatives,” Journal Chememistry Heterocyclic Compounds, Vol. 26, 2004, pp. 1051-1060. doi:10.1007/BF00472492

[5]   M. E. A. Zaki, A. A. Fadda, Kh. Samir and F. A. Amer, “Nitriles in Organic Synthesis: A Convenient Route to Some Heterocycles Incorporating a Benzothiazole Moiety,” Phosphorus, Sulfur and Silicon and the Related Elements, Vol. 181, No. 8, 2006, pp. 1815-1823. doi:10.1080/10426500500542828

[6]   A. A. Fadda, H. A. Etman, A. A. Sarhan and S. A. El-Hadidy, “Synthesis of Novel 1,2,3,4-Tetrahydrocar-bazole Derivatives of Biological Interest,” Phosphorus, Sulfur and Silicon and the Related Elements, Vol. 185, No. 3, 2010, pp. 526-536. doi:10.1080/10426500902839863

[7]   A. A. Fadda, M. Hammouda, E. M. Afsah and A. A. Hanash, “Nitriles in Organic Synthesis: Synthesis of New Benzothiazole Derivatives of Biological Interest,” Phosphorus, Sulfur and Silicon and the Related Elements, Vol. 185, No. 2, 2010, pp. 433-446. doi:10.1080/10426500902812498

[8]   A. El-Shafei, A. A. Fadda, A. M. Khalil, T. A. E. Ameen and F. A. Badria, “Synthesis, Antitumor Evaluation, Molecular Modeling and Quantitative Structure-Activity Relationship (QSAR) of Some Novel Arylazopyrazolodiazine and Triazine Analogs,” Bioorganic & Medicinal Chemistry, Vol. 17, No. 14, 2009, pp. 5096-5105. doi:10.1016/j.bmc.2009.05.053

[9]   A. A. Fadda, F. A. Badria and K. M. El-Attar, “Synthesis and Evaluation of Curcumin Analogues as Cytotoxic Agents,” Medicinal Chemistry Research, Vol. 19, 2010, pp. 413-430. doi:10.1007/s00044-009-9199-3

[10]   R. Kuttan, P. Bha-numathy, K. Nirmala and M. C. George, “Potential Anti-cancer Activity of Turmeric (Curcuma longa),” Cancer Letter, Vol. 29, 1985, pp. 197-202. doi:10.1016/0304-3835(85)90159-4

[11]   R. A. Tapia, L. Alegria, C. D. Pessoa, C. Salas, M. J. Cortés, J. A. Valderrama, M.-E. Sarciron, F. Pautet, N. Walchshofer and H. Fillion, “Synthesis and Antiprotozoal Activity of Naphthofuranquinones and Naphthothiophenequinones Containing a Fused Thiazole Ring,” Bioorganic & Medicinal Chemistry, Vol. 11, No. 10, 2003, pp. 2175-2182. doi:10.1016/S0968-0896(03)00122-6

[12]   H. Sara?oglu, C. Davran, S. Soylu, ?. Anda?, H. Bati and N. ?aliskan, “3-[2,4-Dinitrophenyl)hydrazono]butane-2-one Oxime,” Acta Crystallography, Vol. E60, 2004, pp. 1307-1309.

[13]   R. F. Japp and F. Klingemann, “Ueber Benzolazound Benzolhydrazofetts?uren,” Chemische Berichte, Vol. 20, No. 4, 1887, pp. 2942-2944. doi:10.1002/cber.188702002165

[14]   V. P. Litvinov, “Thienopyrimidines: Synthesis, Properties, and Biological Activity,” Journal Russian Chemical Bulletin, Vol. 53, No. 3, 2004, pp. 487-516. doi:10.1023/B:RUCB.0000035630.75564.2b

[15]   M. A. Metwally, E. Abdel-Latif and S. Bondock, “Thiocarbamoyl Derivatives as Synthons in Heterocyclic Synthesis,” Sulfur Chemistry, Vol. 28, No. 4, 2007, pp. 431-466. doi:10.1080/17415990701397767

[16]   E. Abdel-Latif and F. A. Amer, “Synthesis of Some 4-Arylazo-3-hydroxythiophene Disperse Dyes for Dyeing Polyester Fabrics,” Monatshefte für Chemie, Vol. 139, No. 5, 2008, pp. 561-567. doi:10.1007/s00706-007-0722-2

[17]   M. A. Metwally, E. Abdel-Latif and F. A. Amer, “Synthesis and Reactions of Some Thiocarbamoyl Derivatives,” Journal of Sulfur Chemistry, Vol. 26, No. 3, 2003, pp. 119-126.

[18]   A. Hantzsch and H. Weber, “Pyridins der Thiophenreihe,” Chemische Berichte, Vol. 20, 1887, pp. 3118-3132. doi:10.1002/cber.188702002200

[19]   A. A. Fadda, F. A. Amer, M. E. A. Zaki and Kh. Samir, “Revised Synthesis of Some New Derivatives of Biological Interest 2-Heterocyclic Benzothiazolyl Derivatives of Biological Interest,” Phosphorus, Sulfur and Silicon and the Related Elements, Vol. 155, 1999, pp. 59-66. doi:10.1080/10426509908044970

[20]   K. R. Sheeja, G. Kuttan and R. Kuttan, “Cytotoxic and Antitumour Activity of Berberin,” Amala Research Bulletin, Vol. 17, 1997, pp. 73-76.

[21]   P. Sur and D. K. Ganguly, “Tea Plant Root Extract (TRE) as an Antineoplastic Agent,” Planta Medicinal, Vol. 60, 1994, pp. 106-109. doi:10.1055/s-2006-959427

[22]   I. Jarak, M. Kralj, I. Piantanida, L. ?uman, M. ?ini?, K. Paveli? and G. Karminski-Zamola, “Novel Cyano- and Amidino-Substituted Derivatives of Thieno[2,3-b]- and Thie-no[3,2-b]thiophene-2-carboxanilides and Thieno- [3′, 2′:4,5]thieno- and Thieno[2′,3′:4,5]thieno [2,3-c]quinolones: Synthesis, Photochemical Synthesis, DNA Binding, and Antitumor Evaluation,” Bioorganic & Medicinal Chemistry, Vol. 14, No. 8, 2006, pp. 2859-2868. doi:10.1016/j.bmc.2005.12.004

[23]   T. Galbadage and P. S. Hartman, “Repeated Temperature Fluctuation Extends the Life Span of Caenorhabditis Elegans in a Daf-16-Dependent Fashion,” Ageing and Development, Vol. 129, No. 9, 2008, pp. 507-514. doi:10.1016/j.mad.2008.04.012