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Synthesis and Reactions of Some New Heterocycles of Expected Biological Activity / Sobhy Mohamed Gomha Mohamed ; Supervised Iklass Abbas , Magda Abdallah , Sayed Riyadh

By: Contributor(s): Language: Eng Publication details: Cairo : Sobhy Mohamed Gomha Mohamed , 2006Description: 237P : ill ; 30cmOther title:
  • تحضير وتفاعلات بعض المركبات الحلقية غير المتجانسة الجديدة المتوقع لها نشاط بيولوجى [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (PH.D.) - Cairo University - Faculty Of Science - Department Of Organic Chemistry Summary: The first project represents the preparation of two series of 7 - arylazo - 7H - 3 - (2 - methyl - 1H - indol - 3 - yl) - pyrazolo[5 , 1 - c][1 , 2 , 4]triazol - 6 (5H) - ones 7 and 7 - arylhydrazono - 7H - 3 - (2 - methyl - 1H - indol - 3 - yl) - [1 , 2 , 4]triazolo[3 , 4 - b][1 , 3 , 4] thiadiazines 9 via reactions of 4 - amino - 5 - mercapto - 3 - (2 - methyl - 1H - indol - 3 - yl) - 1 , 2 , 4 - triazole 5 with each of ethyl N - arylhydrazono - chloroacetate 1A and N - aryl - 2 - oxoalkanehydrazonoyl halides 1B , 1D - F , respectively (Schemes 1 , 2) The mechanism that accounts for the formation of the products was proposedAlso , the biological activity of some of these products was evaluated
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.Ph.D.2006.So.S. (Browse shelf(Opens below)) Not for loan 01010110045760000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.Ph.D.2006.So.S. (Browse shelf(Opens below)) 45760.CD Not for loan 01020110045760000

Thesis (PH.D.) - Cairo University - Faculty Of Science - Department Of Organic Chemistry

The first project represents the preparation of two series of 7 - arylazo - 7H - 3 - (2 - methyl - 1H - indol - 3 - yl) - pyrazolo[5 , 1 - c][1 , 2 , 4]triazol - 6 (5H) - ones 7 and 7 - arylhydrazono - 7H - 3 - (2 - methyl - 1H - indol - 3 - yl) - [1 , 2 , 4]triazolo[3 , 4 - b][1 , 3 , 4] thiadiazines 9 via reactions of 4 - amino - 5 - mercapto - 3 - (2 - methyl - 1H - indol - 3 - yl) - 1 , 2 , 4 - triazole 5 with each of ethyl N - arylhydrazono - chloroacetate 1A and N - aryl - 2 - oxoalkanehydrazonoyl halides 1B , 1D - F , respectively (Schemes 1 , 2) The mechanism that accounts for the formation of the products was proposedAlso , the biological activity of some of these products was evaluated

Issued also as CD

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