| 000 | 02938cam a2200313 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 008 | 160518s2015 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.2015.No.H | ||
| 100 | 0 | _aNora Ali Mohamed Ali Anter | |
| 245 | 1 | 0 |
_aHeteroarylnitrilimines and related intermediates in the synthesis of heterocyclic compounds with expected biological activity / _cNora Ali Mohamed Ali Anter ; Supervised Hamdi M. Hassaneen , Sherif M. Sherif |
| 246 | 1 | 5 | _aا{uئإؤئ}{uئإإ٨}{uئآئئ}{uئإ٩٨}{uئإءإ}{uئآئإ}{uئإؤإ} ا{uئآئإ}{uئإإ٤}{uئآئئ}{uئإإ٨}{uئإ٨إ}ت {uئإأئ}{uئآئئ}{uئإءإ} {uئإإ٣}{uئإ٩٨}{uئإء٠}{uئإ٨إ}{uئإإ٧}{uئإآ٤}{uئإ٩٤} ا{uئإؤئ}{uئإء٤}{uئإإ٠}{uئإؤ٨}{uئإ٩٤} و ا{uئإؤئ}{uئإإإ}{uئإآ٣}{uئإ٨إ}{uئإ٨آ}{uئإأ٢} ا{uئإؤئ}{uئإإ٤}{uئإ٩٨}{uئإآ٨}{uئإ٨إ}{uئإ٩١}{uئآءؤ}{uئآءآ} {uئإؤ٣}{uئإئ٠} {uئإ٩٧}{uئإء٤}{uئإأ٠}{uئآئئ}{uئإءإ} {uئإإ٣}{uئإءإ}{uئإؤآ}{uئإ٩٢}{uئإ٨إ}ت {uئإء٣}{uئإإ٠}{uئإؤ٨}{uئآئئ}{uئآءآ} {uئإأئ}{uئآئئ}{uئإءإ} {uئإإ٣}{uئإ٩٨}{uئإء٠}{uئإ٨إ}{uئإإ٧}{uئإآ٤}{uئإ٩٤} و ا{uئإؤئ}{uئإإ٤}{uئإ٩٨}{uئإإإ}{uئإؤ٧}{uئإأء} {uئإؤئ}{uئآءؤ}{uئإ٨إ} {uئإإ٧}{uئإآ٨}{uئإ٨إ}ط {uئإ٩١}{uئآئئ}{uئإإإ}{uئإؤئ}{uئإإإ}{uئإ٩ئ}{uئإئ٠} |
| 260 |
_aCairo : _bNora Ali Mohamed Ali Anter , _c2015 |
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| 300 |
_a82 Leaves ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry | ||
| 520 | _aThe present dissertation describes the utitity of heterocyclic hydrazonoyl halides 1A,B in the synthesis of a new enaminones 3A,B which used for the synthesis of various bipyrazole 8, 13, 14 and pyrazolopyridazine derivatives 10,15. A new 5- amino- 4- iminopyrazolo [3, 4- d] pyrimidine 18A,B was prepared and used in the synthesis of 1, 9- diarylpyrazolo [4,3 - e] 1, 2, 4- triazolo [1, 5- c] pyrimidine 19, 20, 21. Also, triazolo [4, 3- b] [1, 2, 4] triazin - 7- one derivatives 30 and spiropyrazolines 32 were prepared from reaction of heterocyclic hydrazonoyl halides 1A,B with 3- thioxo - 1, 2, 4- triazin - 5- ones 22 and 5- arylmethylene - 3- phenyl - 4- oxothiazole - 2- thione 31, respectively. The structures of the compounds were established on the basis of elemental and spectral analyses as well as their chemical reactions | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aCycloaddition reactions | |
| 653 | 4 | _aEnaminones | |
| 653 | 4 | _aHydrazonoyl halides | |
| 700 | 0 |
_aHamdi M. Hassaneen , _eSupervisor |
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| 700 | 0 |
_aSherif M. Sherif , _eSupervisor |
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| 905 |
_aNazla _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c56537 _d56537 |
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