Synthesis of bis (difunctional) compounds as versatile precursors for Novel Bis heterocycles / Amna Mohamed Abdella Ali ; Supervised Ahmed Helmy Mahmoud Elwahy , Ismail Abdelshafy Abdelhamid
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TextLanguage: English Publication details: Cairo : Amna Mohamed Abdella Ali , 2016Description: 90 P. ; 25cmOther title: - تشييد مركبات ثنائية و متماثلة (ثنائية المجموعة الوظيفية) كبادئات خصبة لمركبات حلقية غير متجانسة جديدة ثنائية و متماثلة [Added title page title]
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Thesis
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.10.M.Sc.2016.Am.S (Browse shelf(Opens below)) | Not for loan | 01010110071151000 | ||
CD - Rom
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.10.M.Sc.2016.Am.S (Browse shelf(Opens below)) | 71151.CD | Not for loan | 01020110071151000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry
An efficient and convenient method for the synthesis of bis (4H-chromene-3-carbonitrile) derivatives. The synthetic pathway involves one pot, multi-component reaction of bis- aldehydes, malononitrile, and dimedone in the presence of a catalytic amount of piperidine. A stepwise approach for the synthesis of the target compounds was also investigated. Bis (2- benzylidene-1H-indene)-1,3-(2H)-dione derivatives were obtained as the main products as a result of reaction of the bis(arylidenemalononitriles) with indandione. The anti-influenza H5N1 virus activities of the newly prepared bis-chromene derivatives are also investigated. An efficient and convenient route for the synthesis of novel bis dihydropyrano[3,2- c]chromenes is reported. The synthetic pathway involves one pot, multi-component reaction of bis-aldehydes, malononitrile, and 4-hydroxycoumarin in the presence of pyridine or acetic acid in the presence of sodium acetate. A stepwise approach for the synthesis of the target compounds was also investigated. The structures of all compounds are confirmed based on the different spectral tools
Issued also as CD
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