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Synthesis and biological activity studies of new heterocyclic compounds containing azolo-azine derivatives / Elshimaa Mohmed Elsaied Eid ; Supervised Hamed Abdelrhim Ead , Huwaida M. E. Hassaneen

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Elshimaa Mohmed Elsaied Eid , 2015Description: 75 P. ; 25cmOther title:
  • التشيد والنشاط البيولوجى لمركبات جديدة غير متجانسة الحلقة تحتوى على مشتقات الازول-ازين [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: This thesis introduces Synthesis of new derivatives of dispiropyrrolidinyl oxindole 6a-j and dispiropyrrolizinyl oxindole 8a-j through 1,3-dipolar cycloaddition reaction of azomethine ylides generated from isatin, sarcosine/ L-proline through decarboxylative route with dipolarophile 4a-j. All the newly synthesized compounds were evaluated for their antimicrobial activities and also their minimum inhibitory concentration (MIC) against most of test organisms was performed. Amongst the tested compounds displayed excellent activity against all the tested microorganisms
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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.2015.El.S (Browse shelf(Opens below)) Not for loan 01010110068085000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2015.El.S (Browse shelf(Opens below)) 68085.CD Not for loan 01020110068085000

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

This thesis introduces Synthesis of new derivatives of dispiropyrrolidinyl oxindole 6a-j and dispiropyrrolizinyl oxindole 8a-j through 1,3-dipolar cycloaddition reaction of azomethine ylides generated from isatin, sarcosine/ L-proline through decarboxylative route with dipolarophile 4a-j. All the newly synthesized compounds were evaluated for their antimicrobial activities and also their minimum inhibitory concentration (MIC) against most of test organisms was performed. Amongst the tested compounds displayed excellent activity against all the tested microorganisms

Issued also as CD

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