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Home > حضرت داود علیہ السلام سے متعلق تفسیری روایات کا تحقیقی مطالعہ

حضرت داود علیہ السلام سے متعلق تفسیری روایات کا تحقیقی مطالعہ

Thesis Info

Author

آمنہ جاوید

Supervisor

ایس ایم شریف

Program

Mphil

Institute

Riphah International University

Institute Type

Private

Campus Location

Faisalabad Campus

City

Faisalabad

Province

Punjab

Country

Pakistan

Thesis Completing Year

2017

Thesis Completion Status

Completed

Page

221 . : ill. ; 30 cm.

Subject

Islam

Language

Urdu

Other

Submitted in fulfillment of the requirements for the degree of Master of Philosophy in Islamic Studies.; Includes bibliographical references; Thesis (M.Phil)--Riphah International University, 2017; Urdu; Call No: 297 AMN

Added

2021-02-17 19:49:13

Modified

2023-02-19 12:33:56

ARI ID

1676712158604

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حضورِ شاہؐ کھڑا ہوں میں نعت لکھتے ہوئے

حضورِ شاہ ؐ کھڑا ہوں میں نعت لکھتے ہوئے
قسم خدا کی بڑا ہوں میں نعت لکھتے ہوئے

خطائیں اپنی جو سوچوں تو کانپ اُٹھتا ہوں
زمیں کے بیچ گڑا ہوں میں نعت لکھتے ہوئے

درِ خدا بھی ملا ہے ترے ہی در کے طفیل
ترے ہی در پہ کھڑا ہوں میں نعت لکھتے ہوئے

یہ کائنات ہے انگشتری کی صورت میں
نگیں مثال جَڑا ہوں میں نعت لکھتے ہوئے

میں نعت لکھنے کے قابل کہاں ہوا عابدؔ
سو خود سے یوں بھی لڑا ہوں میں نعت لکھتے ہوئے

نباتات قرآن وحدیث جدید سائنس کی روشنی میں

The present study work is about importance of plants in the light of Quran, A hadith and modern science Plants are an important means of survival. Without them, life is not only difficult but impossible. The very first tree was mention by Allah when the Hazrat Aadam Eli Hisslam was in the heaven a number of plant was mention by Quran o Hadith and other botanical books. Plants are main source of nutrition for human being, animals and curative plants are beauty of our planet. Their medicinal values are mention by Quran and Prophat Hazrat Muhammad صلى الله عليه وسلم proved by modern science. Many books and research paper have been written on plants with the passage of time the direction of research has also changed, as in the case of epidemics, likewise Corona has opened a new avenue of research that has resorted to herbal remedies, among other therapies. Such current research work is part of a series that sheds light on various aspects of plants.

Transition Metal-Catalyzed Borylation of Aromatics

Selective functionalization of hydrocarbons represents a long-standing challenge in the synthetic world. Transition metal-catalyzed reactions, such as transformation of C–H/ C– X bond to C–B bond has emerged as potent tool towards this goal during the last few decades. Especially the Ir-catalyzed aromatic C-H activation/borylaytion provides unique selectivity which is complemantary to those found in the traditional synthetic routes. Sterically governed regioselective control in this new synthetic tool allows the synthesis of (hetero)aromatic compounds which are difficult to access by the conventional routes. In the current work, we have utilized this methodology to gain facile access to new aromatic building blocks with better atom & step economy. One study presents the synthesis of hydroxybenzoates. Hydroxybenzoates are widely used as preservatives and antiseptics in the food and pharmaceutical industry. However, strategies focusing on the direct synthesis of 2,6- and 2,3-disubstituted hydroxybenzoates are lacking in literature. Herein we report an efficient protocol employing iridium-catalyzed C–H borylation/oxidation of commercially available benzoic acid/ester substrates. This route provides facile access to halogen decorated para-/meta-hydroxybenzoates as the synthesis of akin compounds is laborious by traditional approaches. Second project targets the synthesis of boscalid analogs. Boscalid is an extensively used fungicide for crop protection. Traditional routes of boscalid synthesis involve precursors that need pre-functionalization of arenes, which affects the step economy and overall efficiency. The aim of this study is to develop boscalid analogues from readily available hydrocarbon feedstock without pre-functionalization. Sequential Ir-catalyzed C–H borylation of arenes and Suzuki coupling provide biphenyl amines which on amidation produce boscalid analogues in good yield. Synthesized compounds are further evaluated by molecular docking to gain insight into the binding pocket of protein. The In-vitro studies of the analogs are carried out against Fusarium moniliforme and few of the synthesized compounds provided superior inhibition on potato dextrose agar (PDA) plates. Next, Ir-catalyzed C-H borylation of CF3 substituted pyridines is reported. The versatility of the methodology is demonstrated by the use of various substitution patterns in the substrate molecule. Based on the steric evaluation, selective positions of CF3 substituted pyridines are functionalized. Several functional groups like halo, ester, methoxy and amino are compatible with this methodology. Chiral boronic esters are indispensable building blocks owing to their versatile transformations and immense applications in medicinal and material chemistry. Herein, we also disclose Pd-catalyzed chiral borylation of aryl halides, whereby numerous substrates bearing broad range of functional groups are found to be compatible for the developed approach. Aryl/hetero aryl chiral boronic esters are obtained in moderate to excellent yield. The resulting chiral boronic esters can serve as significant precursors in asymmetric synthesis.