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آنکھ سے دور سہی دل کے قریں رہنے دے

آنکھ سے دُور سہی، دل کے قریں رہنے دے
میری ہر سانس میں تو خود کو مکیں رہنے دے

میں کہ اک عکس ہوں گمنام سا پس منظر ہوں
کب کہاں کیسے کسی طور کہیں رہنے دے

اک نظر مجھ پہ مرے ماہِ منیر ایسی ہو
کب طلب میں نے کیا زر یا نگیں، رہنے دے

میں ہوں اس قافلۂ عشق سے بچھڑا راہی
میرا کب ٹھور ٹھکانہ ہے کہیں، رہنے دے

تجھ سے منسوب ہوئی، تجھ سے ہی منسوب رہوں
غیر کے آگے جھکے گی یہ جبیں، رہنے دے

دل میں یا آنکھ میں یا دستِ حنائی میں فضاؔ
تیری مرضی ہے جہاں چاہے، وہیں رہنے دے

السیرة النبوية از احمد بن زینی دحلان (م ۱۳۰۴ھ) کے مباحث فقہیہ کا تحقیقی جائزہ

Ahmad bin zeni Dahlan was born in Mecca on 1231 AH. He was a great scholar of Tafseer, Hadith, Fiqh and Sirah. His book "السیرۃالنبویۃ "is a wonderful piece of writing on sirah of Holy Prophet (PBUH). This book has got a significant place in sirah literature. In this book, Author discusses almost all the aspects of the life of Prophet Muhammad (PBUH), like his attributes, miracles, incidents and battles etc. One of zeni dahlan’s modes of sirah writing is that he derives juristic implications and lessons from the events of sirah which can be called Fiqh al sirah in modern terminology. This article intends to explore the mode of Fiqh al sirah in respect with “Al sirah al nabawiyyah” written by Ahmad bin Zeni Dahlan.

Synthesis, Characterization and Biological Screening of Some New N and O Containing Heterocyclic Compounds

The derivatives of isocoumarins, coumarins and 1,2,4-triazoles are prominent biological agents used as a cure against a number of human ailments. The present work deals with their synthesis. 3-(Halobenzyl)isocoumarins (5a-i) were synthesized by condensation of 2-(halophenyl)acetyl chlorides (3a-i) with homophthalic acid (4) at elevated temperature. 3-(Halobenzyl)isocoumarins (5a-i) were converted into 3-(halobenzyl)-3,4- dihydroisocoumarins (8a-i) via ketoacids (6a-i) and hydroxyacids (7a-i). 3- (Halobenzyl)isocoumarins (5a-i) converted to their thio analogues (10a-i) by treating with Lawesson’s reagent (11) while their nitrogen analogues (12a-i) were obtained by passing ammonia into the solution of 3-(halobenzyl)isocoumarins (5a-i) in 2-ethoxy ethanol. These synthesized compounds were evaluated for urease inhibition and anti- inflammatory activity. 3-(Halobenzyl)isocoumarins (5a-i) and ketoacids (6a-i) exhibited moderate urease inhibition activity. While others showed non significant activity. The isoquinolinone (12c) showed anti-inflammatory activity higher than standard compound i-e indomethacin while all other compounds showed non significant anti-inflammation. Reaction of hitherto unknown 4-chloro-3-(2,2,2-trifluoroacetyl)-2H-chromen-2-one (16a) with different commercially availble anilines (19a-l) gave respective 3-(trifluoroacetyl) - 4-(arylamino)-2H-chromen-2-one (20a-l) which were then successfully cyclized to 7- (trifluoromethyl)-6H-chromeno[4,3-b]quinolin-6-ones (21a-l) using conc. H2SO4. The synthesis of 4-aryl-3-(trifluoroacetyl)-2H-chromen-2-ones (18a-n) was accomplished by Suzuki coupling reaction of 4-chloro-3-(2,2,2-trifluoroacetyl)-2H-chromen-2-one (16a) and aryl boronic acids (17a-n). Synthesis of 1,2,4-triazoles (31a-o) was carried out by dehydrative cyclization of thiosemicarbazides (20a-o) which in turn were synthesized by addition of hydrazides (29a-i) on isothiocyanate (27m-n). These triazoles showed moderate antibacterial activity. Finally the synthesized 1,2,4-triazoles (31a-o) were evaluated for their toxicity and these showed low toxicity.
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