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Application of diazo coupling reactions in synthesis of new heterocyclic compounds of pharmaceutical interest / Heba Elsayed Ahmed Teba ; Supervised Mohammed A. Shaaban , Nadia A. Abdo , Aliaa M. Kamal

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Heba Elsayed Ahmed Teba , 2014Description: 107 P. : charts ; 25cmOther title:
  • تطبيق تفاعل اقتران الديازين فى تشييد مركبات جديده حلقية غير متجانسة ذات اهمية صيدلية [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Organic Chemistry Summary: This thesis comprises five parts, the first part is an introduction about diazocoupling reactions and synthesis of benzimidazoles. The second part clarifies the rationale for the synthesis of the targeted compounds. The third part deals with the theoretical diazocoupling of the experimental work in preparation of compounds {u2160} - XX{u2160}. The structures were supported by elemental analysis, {u2160}R, ¹H NMR, ¹³C NMR mass spectral data and TLC monitoring. In the fifth part, biological activity was evaluated in - vitro growth of three human tumor cell lines, MCF -7) (NC{u2160} - H460), and (SF - 268) and compared with doxorubicin
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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 Cai01.08.04.M.Sc.2014.He.A (Browse shelf(Opens below)) Not for loan 01010110064072000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.08.04.M.Sc.2014.He.A (Browse shelf(Opens below)) 64072.CD Not for loan 01020110064072000

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

This thesis comprises five parts, the first part is an introduction about diazocoupling reactions and synthesis of benzimidazoles. The second part clarifies the rationale for the synthesis of the targeted compounds. The third part deals with the theoretical diazocoupling of the experimental work in preparation of compounds {u2160} - XX{u2160}. The structures were supported by elemental analysis, {u2160}R, ¹H NMR, ¹³C NMR mass spectral data and TLC monitoring. In the fifth part, biological activity was evaluated in - vitro growth of three human tumor cell lines, MCF -7) (NC{u2160} - H460), and (SF - 268) and compared with doxorubicin

Issued also as CD

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