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Synthesis and reactions of New heterocyclic compounds as bases for some nucleosides with expected biological activities / Naglaa Salem Elsayed Ibrahim ; Supervised Abdelsamei M. Abdelfattah , Ahmed Saleh Ali Elsayed

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Naglaa Salem Elsayed Ibrahim , 2010Description: 120 P. : charts ; 25cmOther title:
  • تحضير و تفاعل مركبات عضوية جديدة غير متجانسة الحلقة كقواعد لتحضير بعض النيوكلوسيدات و المتوقع لها نشاط بيولوجى [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry Summary: This work has been carried out to investigate the synthesis of some new nicotinonitrile derivatives, as well as, 5,6-dimethyl-4-(4-methoxy-phenyl) pyrazolo[3,4-b] pyridin-3-amine, that was utilized as a good synthone for the preparation of different heterocyclic compounds, by its reaction with various electrophiles. In addition, investigating the analgesic and anti-inflammatory activities of some selected compounds
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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.2010.Na.S (Browse shelf(Opens below)) Not for loan 01010110053805000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2010.Na.S (Browse shelf(Opens below)) 53805.CD Not for loan 01020110053805000

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

This work has been carried out to investigate the synthesis of some new nicotinonitrile derivatives, as well as, 5,6-dimethyl-4-(4-methoxy-phenyl) pyrazolo[3,4-b] pyridin-3-amine, that was utilized as a good synthone for the preparation of different heterocyclic compounds, by its reaction with various electrophiles. In addition, investigating the analgesic and anti-inflammatory activities of some selected compounds

Issued also as CD

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