| 000 | 01643cam a2200325 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223031737.0 | ||
| 008 | 170620s2016 ua do 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.2016.Ay.U | ||
| 100 | 0 | _aAya Elsayed Elsayed Khedr | |
| 245 | 1 | 0 |
_aUses of nitriles and carbonyl compounds in the synthesis of biologically active heterocyclic compounds / _cAya Elsayed Elsayed Khedr ; Supervised Raafat Milad Mohareb |
| 246 | 1 | 5 | _aاستخدامات مركبات النيتريل و الكاربونيل لتحضير المركبات غير متجانسة الحلقة ذات النشاط البيولوجى |
| 260 |
_aCairo : _bAya Elsayed Elsayed Khedr , _c2016 |
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| 300 |
_a139 P. : _bcharts , photographs ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry | ||
| 520 | _aIn this work the reaction of ethylacetoacetate (1) with Ü-naphthylamine (2) gave the N-(Naphthalen-1-yl)-3-oxobutanamid (3). The latter products underwent a series of heterocyclization reactions to yield pyridine, pyran, thiophene and pyrazole derivatives. The antitumor evaluations of the newly synthesized products against three cancer cell lines were measured | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _a1,3-dicarbonyl compounds | |
| 653 | 4 | _aHeterocycles | |
| 653 | 4 | _aSynthesis | |
| 700 | 0 |
_aRaafat Milad Mohareb , _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 |
_c61359 _d61359 |
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