| 000 | 019770000a22003490004500 | ||
|---|---|---|---|
| 003 | EG-GICUC | ||
| 005 | 20250223031112.0 | ||
| 008 | 060917s2006 ua a 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.2006.Am.U. | ||
| 100 | 0 | _aAmr Salah AbouZeid | |
| 245 | 1 | 0 |
_aNew routes for synthesis of biologically interestingpolyfunctional heteroaromatics utilizing an enamine precursor / _cAmr Salah AbouZeid ; Supervised Mohamed Helmy Elnagdi , Fatma Mohamed Manhi |
| 246 | 1 | 5 | _aطرق جديدة لتخليق ا لحلقيات غير المتجانسة عديدة المجموعة الدالة وذات النشاط البيولوجى المتوقع باستخدام الاينامينات كمواد اولية |
| 260 |
_aCairo : _bAmr Salah AbouZeid , _c2006 |
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| 300 |
_a157P : _bill ; _c30cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty Of Science - Department Of Organic Chemistry | ||
| 520 | _a2 - Acetylnaphthalene 1 condenses with dimethylformamide dimethylacetal (DMFDMA) yielding enaminone 2 , best yield was obtained by heating in a domestic microwave oven at full power for 5 minutes (85in hundred) The formed E enaminone 2 reacted with 2amino4methylthiazole 3 , 4aminopyridine 4 and Osubstituted aniline 5ac yielding the Z enaminones , predomination of Z form due to the fixation of this form by hydrogen bond (cfFigure 1) ; Although 2aminobenzothiazole 9 afforded a mixture of E enaminone 10 and Z - enaminone 11in ratio 4 : 6 as indicated from 1H NMR (cfFigure 2) | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aEnaminones | |
| 653 | 4 | _apyrazoles | |
| 653 | 4 | _apyrimidines | |
| 653 | 4 | _aquinolinone | |
| 700 | 0 |
_aFatma Mohamed Manhi , _eSupervisor |
|
| 700 | 0 |
_aMohamed Hilmy Elnagdi , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aAmira _eCataloger |
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| 905 |
_aMustafa _eRevisor |
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| 942 |
_2ddc _cTH |
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| 999 |
_c48444 _d48444 |
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