Search In this Thesis
   Search In this Thesis  
العنوان
Synthesis of some azoles, azines and its fused derivatives with expected biological activity /
الناشر
Aly Mahmoud Mohamed Mohamed ,
المؤلف
Aly Mahmoud Mohamed Mohamed
هيئة الاعداد
باحث / Aly Mahmoud Mohamed Mohamed
مشرف / Abdou O. Abdelhamid
مشرف / NaWafaa M. Hossny dia abdel hamid
مشرف / Wafaa M. Hossny
تاريخ النشر
2017
عدد الصفحات
307 P. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
Chemistry (miscellaneous)
تاريخ الإجازة
7/10/2017
مكان الإجازة
جامعة القاهرة - كلية العلوم - Chemistry
الفهرس
Only 14 pages are availabe for public view

from 200

from 200

Abstract

1-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)ethen-1-one was reacted with thiosemicarbazide, alkyl Carbodithioate, Benzaldehyde and Ethylformate gave thiosemicarbazone, alkyledene hydraziecarbodithioate,5-benzyledene-1,2,3triazole. 1,3,4-thiadiazole derivatives were abtaimed from reaction of alkyladene carbothioate with hydrazonoyl chlorides. Also, hydrazonyl halides were reacted with each of thiosemicarbazone and pyrazolinthioamid to give 5-arylazothiazoles derivative containing 1,2,3-triazole moiety. Howevere, the sodium salt of 3-(5-methyl-1-(p-tolyl)-1H-1,2,3- triazol-4-yl)-3-oxoprop-1-ene-1-oleate was used to synthezed some azolo[1,5-a] pyridenes, azolo[5,1-c] triazines, substituted pyridines. Azido (2-methyl-6-(5-methyl-1-(p-tolyl)-1H- 1,2,3-triazol-4-yl)-4-phenyl-pyridin-3-yl) methanone was reacted with aromatic amines and phenol to give substituted urea and arylcarbmate containing 1,2,3-triazole moiety. All the newly synthesized compounds were established by elemental analysis, spectral data and alternative synthies routes whenever possobile. Same of the srewly synthesized compounds was scrrem to wards macroorganism