hrcak mascot   Srce   HID

Original scientific paper

Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles

M. Y. Yousif ; Department of Chemistry, Faculty of Pharmacy and Faculty of Science, University of Mansaura, Mansaura, Egypt
A. M. Ismail ; Department of Chemistry, Faculty of Pharmacy and Faculty of Science, University of Mansaura, Mansaura, Egypt
M. A. Metwally ; Department of Chemistry, Faculty of Pharmacy and Faculty of Science, University of Mansaura, Mansaura, Egypt
M. M. EI-Kerdawy ; Department of Chemistry, Faculty of Pharmacy and Faculty of Science, University of Mansaura, Mansaura, Egypt

Fulltext: english, pdf (2 MB) pages 309-314 downloads: 80* cite
APA 6th Edition
Yousif, M.Y., Ismail, A.M., Metwally, M.A. & EI-Kerdawy, M.M. (1987). Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles. Croatica Chemica Acta, 60 (2), 309-314. Retrieved from https://hrcak.srce.hr/176360
MLA 8th Edition
Yousif, M. Y., et al. "Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles." Croatica Chemica Acta, vol. 60, no. 2, 1987, pp. 309-314. https://hrcak.srce.hr/176360. Accessed 22 Apr. 2021.
Chicago 17th Edition
Yousif, M. Y., A. M. Ismail, M. A. Metwally and M. M. EI-Kerdawy. "Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles." Croatica Chemica Acta 60, no. 2 (1987): 309-314. https://hrcak.srce.hr/176360
Harvard
Yousif, M.Y., et al. (1987). 'Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles', Croatica Chemica Acta, 60(2), pp. 309-314. Available at: https://hrcak.srce.hr/176360 (Accessed 22 April 2021)
Vancouver
Yousif MY, Ismail AM, Metwally MA, EI-Kerdawy MM. Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles. Croatica Chemica Acta [Internet]. 1987 [cited 2021 April 22];60(2):309-314. Available from: https://hrcak.srce.hr/176360
IEEE
M.Y. Yousif, A.M. Ismail, M.A. Metwally and M.M. EI-Kerdawy, "Syntheses of 4-Substituted-3-Methyl-2-Phenylimidazoles", Croatica Chemica Acta, vol.60, no. 2, pp. 309-314, 1987. [Online]. Available: https://hrcak.srce.hr/176360. [Accessed: 22 April 2021]

Abstracts
Reaction of the title compound I with aromatic aldehydes afforded a,b-unsaturated ketones II, which were allowed to react with cyanoacetamide, ethyl cyanoacetate, hydrazines. Treatment
of I with hydrazines or amines gave V and VI.

Hrčak ID: 176360

URI
https://hrcak.srce.hr/176360

Visits: 164 *