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Synthesis of some New pyrazole - based heterocycles of potential biological activity / Mahmoud Hanafy Mahmoud Hassan Youssef ; Supervised Kamal M. H. Dawood , Taha M. A. Eldebess , Heba S. Elzahabi

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Mahmoud Hanafy Mahmoud Hassan Youssef , 2013Description: 114 P. : charts ; 25cmOther title:
  • تشيد بعض الحلقيات غير المتجانسة ذات النشاط البيولوجى المتوقع المبنية على البيرازول [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 current work is describing a facile and convenient routes for the synthesis of several multi-linked heterocycles containing pyrazole, 1, 3 - thiazole and 1, 3, 4 - thiadiazole moieties which would be expected to have potent biological activities. 4 - (2 - aminothiazol - 4 - yl)- 2, 3 - dimethyl - 1 - phenylpyrazol - 5 - one was a suitable candidate for the synthesis of the planned target molecules. The structures of the obtained new compounds are elucidated with all possible spectral data (IR, MS, ¹H and ¹³C - NMR
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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.2013.Ma.S (Browse shelf(Opens below)) Not for loan 01010110063194000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2013.Ma.S (Browse shelf(Opens below)) 63194.CD Not for loan 01020110063194000

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

The current work is describing a facile and convenient routes for the synthesis of several multi-linked heterocycles containing pyrazole, 1, 3 - thiazole and 1, 3, 4 - thiadiazole moieties which would be expected to have potent biological activities. 4 - (2 - aminothiazol - 4 - yl)- 2, 3 - dimethyl - 1 - phenylpyrazol - 5 - one was a suitable candidate for the synthesis of the planned target molecules. The structures of the obtained new compounds are elucidated with all possible spectral data (IR, MS, ¹H and ¹³C - NMR

Issued also as CD

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