| 000 | 01731cam a2200325 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030937.0 | ||
| 008 | 140226s2013 ua f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aM.Sc | ||
| 099 | _aCai01.12.10.M.Sc.2013.Hu.S | ||
| 100 | 0 | _aHuda Kamel Mahmoud | |
| 245 | 1 | 0 |
_aSynthesis, reactions and biological activities of some perimidine derivatives / _cHuda Kamel Mahmoud ; Supervised Thoraya Abdelreheem Farghaly |
| 246 | 1 | 5 | _aتشييد و تفاعلات و النشاط البيولوجى لبعض مشتقات البريميدين |
| 260 |
_aCairo : _bHuda Kamel Mahmoud , _c2013 |
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| 300 |
_a141 P. ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry | ||
| 520 | _aThe original work of the submitted thesis consists of two new research projects entitled: (1) Site- and regioselectivity of the reaction of hydrazonoyl Chlorides with perimidine-ketene animal. Antimicrobial evaluation of the products and (2) Synthesis, Tautomeric structures and antitumor activity of new perimidines. In the first project: reaction of hydrazonoyl chlorides with perimisine ketene amimal derivative in dioxane in the presence of triethylamine afforded either pyrrolo[1,2-Ü]perimidines or pyrazolyl perimidines depending on the type of hydrazonoyl chloride used | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aHydrazonoyl halide | |
| 653 | 4 | _aPerimidine | |
| 653 | 4 | _aRegioselectivity | |
| 700 | 0 |
_aThoraya Abdelreheem Farghaly , _eSupervisor |
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| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c45197 _d45197 |
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