000 | 01632cam a2200337 a 4500 | ||
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003 | EG-GiCUC | ||
005 | 20250223030811.0 | ||
008 | 130324s2012 ua f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aPh.D | ||
099 | _aCai01.12.10.Ph.D.2012.Ba.S | ||
100 | 0 | _aBasma Saad Baaiu | |
245 | 1 | 0 |
_aSynthesis of some new azole azine and fused azoloazine derivatives with expected biological activity / _cBasma Saad Baaiu ; Supervised Abdelgawad Ali Fahmi , Abdou Osman Abdelhamid |
246 | 1 | 5 | _aتشييد بعض مركبات الآزول والازين وملتحماتها والتأثيرات البيولوجية المتوقعة لها |
260 |
_aCairo : _bBasma Saad Baaiu , _c2012 |
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300 |
_a108P. : _c25cm |
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502 | _aThesis (Ph.D.) - Cairo University - Faculty of Science - Department of Organic Chemistry | ||
520 | _a2,3 - Dihydro - 1,3,4 - thiadiazoles 2,3-dihydro- 1.2.4-selenadiazoles and triazolino[4,3-a] pyrimidines containing benzofuran moiety were prepared from the reaction of 2-(2- phenylhydrazono)-1- (5-bromobenzofuran-2-y1)-2-chloroethanone with each of potassium thiocyanate potassum selenocyanate alky1 carbodithioate and pyrmidine-2-thione derivatives | ||
530 | _aIssued also as CD | ||
653 | 4 | _a1,3,4-thiadiazoles | |
653 | 4 | _aHydrazonoy1 halides | |
653 | 4 | _aNitrilimines | |
700 | 0 |
_aAbdelgawad Ali Fahmi , _eSupervisor |
|
700 | 0 |
_aAbdou Osman Abdelhamid , _eSupervisor |
|
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 |
_c42208 _d42208 |