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Synthesis of some new heterocyclic compounds from available nitriles with expected biological activity / Salwa Magdy Ahmed Eldaly ; Sypervised Fathy M. Abdelrazek

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Salwa Magdy Ahmed Eldaly , 2014Description: 89 P. : charts ; 25cmOther title:
  • "تشييد بعض المركبات غير متجانسة الحلقة الجديدة من نتيريلات متوافرة ذات نشاط بيولوجى متوقع" [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry Summary: The original work of this thesis includes the study of the reaction of 1- cyanoacetylpyrazole 1 with phenyl isothiocyanate followed by the addition of different halocarbonyl compounds to afford thiazole and oxathiepine derivatives and the reaction of the arylhydrazo derivative of this compound with phenylene-1,4-diamine to give the compounds 13. Refluxing of 13 with hydrazine hydrate afforded aminotriazoles 15. Compound 1 reacts with different arylazo derivatives of aminopyrazoles to afford the corresponding pyrazolo[1,5-a]pyrimidine derivatives. Compound 21 reacted with phenyl isothiocyanate followed by the addition of different halocarbonyl compounds, the N-alkylated derivatives 24 were obtained.The reaction of 1 with 4- aminoacetophenone afforded the cyanoacetamide derivative 26 which underwent different chemical reactions to give arylidines, iminochromenes, di-arylidenes, di- iminochromenes, di-arylazo compounds and di-thiazoles. The antitumor activity of some of the newly synthesized compounds was investigated in vitro besides Molecule rmodeling (using MOE 2008)
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2014.Sa.S (Browse shelf(Opens below)) Not for loan 01010110064013000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2014.Sa.S (Browse shelf(Opens below)) 64013.CD Not for loan 01020110064013000

Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry

The original work of this thesis includes the study of the reaction of 1- cyanoacetylpyrazole 1 with phenyl isothiocyanate followed by the addition of different halocarbonyl compounds to afford thiazole and oxathiepine derivatives and the reaction of the arylhydrazo derivative of this compound with phenylene-1,4-diamine to give the compounds 13. Refluxing of 13 with hydrazine hydrate afforded aminotriazoles 15. Compound 1 reacts with different arylazo derivatives of aminopyrazoles to afford the corresponding pyrazolo[1,5-a]pyrimidine derivatives. Compound 21 reacted with phenyl isothiocyanate followed by the addition of different halocarbonyl compounds, the N-alkylated derivatives 24 were obtained.The reaction of 1 with 4- aminoacetophenone afforded the cyanoacetamide derivative 26 which underwent different chemical reactions to give arylidines, iminochromenes, di-arylidenes, di- iminochromenes, di-arylazo compounds and di-thiazoles. The antitumor activity of some of the newly synthesized compounds was investigated in vitro besides Molecule rmodeling (using MOE 2008)

Issued also as CD

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