| 000 | 02898cam a2200337 a 4500 | ||
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| 003 | EG-GiCUC | ||
| 005 | 20250223031602.0 | ||
| 008 | 161023s2016 ua d 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.Do.U | ||
| 100 | 0 | _aDoaa Mohamed Abdelmoniem Hassan | |
| 245 | 1 | 0 |
_aUtility of enamines as precursors for Synthesis of new heterocycles / _cDoaa Mohamed Abdelmoniem Hassan ; Supervised Said Ahmed Soliman Ghozlan , Ismail Abdelshafy Abdelhamid |
| 246 | 1 | 5 | _aاستخدام الاينامينات كبادئات اولية لتحضير حلقات غير متجانسة الحلقة جديدة |
| 260 |
_aCairo : _bDoaa Mohamed Abdelmoniem Hassan , _c2016 |
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| 300 |
_a89 P. : _bcharts ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry | ||
| 520 | _aThe original work of this thesis is composed of three parts. In the first part, a series of N-((1,2,4-triazol-3-yl)-enamine and N-((1,2,3-triazol-4-yl)-enamine were prepared and reacted with Ü,Ý-unsaturated nitriles to yield novel N-(4H-1,2,4-triazol-3-yl)- hexahydroquinoline-3-carbonitrile and their fused and spiro derivatives. Dimroth type rearrangement of the prepared quinoline derivatives was observed in acetic anhydride leading to the formation of substituted pyrimido[4,5-b]quinoline, spiro[indoline-3,5'-pyrimido[4,5- b]quinoline] and spiro[indoline-3,5'-[1,3]oxazino[4,5-b]quinoline] compounds. The second part, A simple and efficient one-pot synthesis of novel thieno[3',2':5,6]pyrimido[1,2- a]quinoline-2-carboxylates and their spirooxindole derivatives were accomplished via the Michael addition reaction of a cyclic Ý-enaminone incorporating thiophene moiety with Ü,Ý- unsaturated nitrile derivatives in EtOH at reflux in the presence of piperidine. Also, novel spirocyclic 2-oxoindole derivatives of thieno[3',2':5,6]pyrimido[1,2-a]quinolone were synthesized by the reaction this cyclic Ý-enaminone with 3-cyanomethylidene 2-oxoindole derivatives in refluxing EtOH. In the third part, The three-component reaction of dimedone, malononitrile dimer and bis-aldehydes in ethanol at reflux in the presence of piperidine afforded bis(5H-chromeno[2,3-b]pyridine-3-carbonitrile) derivatives in excellent yields. The chemical structures of all new synthesized products were confirmed based on the different spectral tools and elemental analysis data | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aHexahydroquinoline | |
| 653 | 4 | _aMichael addition | |
| 653 | 4 | _aÝ-Enaminone | |
| 700 | 0 |
_aIsmail Abdelshafy Abdelhamid , _eSupervisor |
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| 700 | 0 |
_aSaid Ahmed Soliman Ghozlan , _eSupervisor |
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| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
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| 905 |
_aSoheir _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c58263 _d58263 |
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