synthesis of certain imidazo and oxazolopyridines of biological interest / Eman Kamal Ahmed Abd El all ; Supervised Mervat Moustafa Elenany , Samiha Mohamed Aly Roshdy , Osama Metwally Elbadry
Language: English Publication details: Cairo : Eman Kamal Ahmed Abdelall , 2005Description: 180 P. : charts ; 30cmOther title:- تشييد بعض مركبات الاميداز والاوكسازولو بيردين ذات الاهمية البيولوجية [Added title page title]
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.04.Ph.D.2005.Em.S (Browse shelf(Opens below)) | Not for loan | 01010110045056000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.04.Ph.D.2005.Em.S (Browse shelf(Opens below)) | 45056.CD | Not for loan | 01020110045056000 |
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Cai01.08.04.Ph.D.2001.Al.S Synthesis of imidazo , pyrimido and triazepinocinnolines of biological interest / | Cai01.08.04.Ph.D.2004.Kh.S. Synthesis of certain heterocyclic compounds as potential DNA intercalators in cancer chemotherapy / | Cai01.08.04.Ph.D.2004.Kh.S. Synthesis of certain heterocyclic compounds as potential DNA intercalators in cancer chemotherapy / | Cai01.08.04.Ph.D.2005.Em.S synthesis of certain imidazo and oxazolopyridines of biological interest / | Cai01.08.04.Ph.D.2005.Em.S synthesis of certain imidazo and oxazolopyridines of biological interest / | Cai01.08.04.Ph.D.2005.La.S. Synthesis of certain heterocyclic novel compounds structurally related to nootropic agents / | Cai01.08.04.Ph.D.2005.La.S. Synthesis of certain heterocyclic novel compounds structurally related to nootropic agents / |
Thesis (Ph.D.) - Cairo University - Faculty of Pharmacy - Department of Organic Chemistry
The present investigation comprises a survey covering the synthesis and biological importance of many imidazo and oxazolo[4 , 5 - b]pyridinesThe thesis involves the preparation of 2 , 3 - diaminopyridine (VIIa) and 2 - amino - 3 - hydroxypyridine (VIIb) and their reaction with p - aminobenzoic to give the imidazo and oxazolopyridines VIIIa , bThe latter were halogenated to afford VIIIc - h
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