الرئيسية › دليل الباحثين › Sarra Boudriga
Sarra Boudriga
الانتماء : University of Monastir
- 37منشورات (انتماء تونسي)
- 82مجموع المنشورات
- 813الاستشهادات
- 16مؤشر h
الملف البحثي
لدى Sarra Boudriga 37 منشور(ات) مفهرسة (2003–2026). تُنشر أعماله أساسًا في «ChemInform»، «Molecules» و«Journal of Molecular Structure». أكثر مقالاته استشهادًا هو «Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylas» (2020)، وقد استُشهد به 133 مرة. 10 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في كندا، فرنسا، السعودية.
هل هذا أنت؟ عرّف بأبحاثك
أنشئ ملفك على DzCademia مجانًا وأضف مقالاتك: ستظهر بسهولة أكبر على Google وفي مساعدي الذكاء الاصطناعي مثل ChatGPT، فيقرؤها ويستشهد بها عدد أكبر من الناس.
إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Crystal structures of chemical compounds
- Crystallography and molecular interactions
- Crystal Structures and Properties
- Multicomponent Synthesis of Heterocycles
- Synthesis and biological activity
المنشورات (37)
- Spiropyrrolizine derivatives as multitarget antidiabetic agents in obese type 2 diabetes: integrated in silico , in vitro , and in vivo evaluation of DPP-4 inhibition and hepatic enzyme modulation
- Evaluation of Betanin on Key Enzymes Related to Obesity, Diabetes, Insulin Signaling Pathway, and Metabolic Disorders: In Vitro, Cellular, and In Silico Study
- Novel triazole-tethered thiazol-4(5H)-one hybrids as potential therapeutics for obesity and type 2 diabetes: in vitro, in vivo, and in silico evaluations
- CdTe-MSA quantum dots prepared by a green hydrothermal route as highly selective ‘turn-off’ fluorescent nanosensors for Lead(II) detection in environmental water monitoring
- Antiobesity and antidiabetes effects of Cyperus rotundus rhizomes presenting protein tyrosine phosphatase, dipeptidyl peptidase 4, metabolic enzymes, stress oxidant and inflammation inhibitory potential
- Asymmetric synthesis of enantiopure tetracyclic dispirooxindolopyrrolidine-piperidones via microwave-assisted multicomponent reaction: Crystallographic analysis, antimicrobial activity and in silico studies
- Exploring the probing capacities of MSA capped CdTe semiconductor quantum dots as optical chemsensors via analytical and isotherms modeling for selective Hg2+ detection
- Synthesis of (Z)-3-Allyl-5-(4-nitrobenzylidene)-2-sulfanylidene-1,3-thiazolidin-4-one and Determination of Its Crystal Structure
- Synthesis of highly functionalized spirooxindole derivatives via multicomponent [3+2] cycloaddition reactions
- List of contributors
- Synthesis of Tetracyclic Spirooxindolepyrrolidine-Engrafted Hydantoin Scaffolds: Crystallographic Analysis, Molecular Docking Studies and Evaluation of Their Antimicrobial, Anti-Inflammatory and Analgesic Activities
- Antimicrobial Activity and DFT Studies of a Novel Set of Spiropyrrolidines Tethered with Thiochroman-4-one/Chroman-4-one Scaffolds
- New spiropyrrolothiazole derivatives bearing an oxazolone moiety as potential antidiabetic agent: Design, synthesis, crystal structure, Hirshfeld surface analysis, ADME and molecular docking studies
- Design of Novel Enantiopure Dispirooxindolopyrrolidine-Piperidones as Promising Candidates toward COVID-19: Asymmetric Synthesis, Crystal Structure and In Silico Studies
- Diversity-Oriented Synthesis of Spiropyrrolo[1,2- a ]isoquinoline Derivatives via Diastereoselective and Regiodivergent Three-Component 1,3-Dipolar Cycloaddition Reactions: In Vitro and in Vivo Evaluation of the Antidiabetic Activity of Rhodanine Analogues
- Antimicrobial Activity and In Silico Molecular Docking Studies of Pentacyclic Spiro[oxindole-2,3′-pyrrolidines] Tethered with Succinimide Scaffolds
- Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylase inhibitors
- Three-Component Access to Functionalized Spiropyrrolidine Heterocyclic Scaffolds and Their Cholinesterase Inhibitory Activity
- Highly diastereoselective construction of novel dispiropyrrolo[2,1- a ]isoquinoline derivatives via multicomponent 1,3-dipolar cycloaddition of cyclic diketones-based tetrahydroisoquinolinium N -ylides
- Straightforward and Highly Diastereoselective Synthesis of a New Set of Functionalized Dispiropyrrolidines Involving Multicomponent 1,3‐Dipolar Cycloaddition with Azomethine Ylides
- Stoichiometry-controlled cycloaddition of nitrilimines with unsymmetrical exocyclic dienones: microwave-assisted synthesis of novel mono- and dispiropyrazoline derivatives
- ChemInform Abstract: Design of Novel Dispirooxindolopyrrolidine and Dispirooxindolopyrrolothiazole Derivatives as Potential Antitubercular Agents.
- ChemInform Abstract: Regio‐ and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines Through Azomethine Ylide Cycloaddition Reaction.
- ChemInform Abstract: Stoichiometry‐Controlled Cycloaddition of Nitrilimines with Unsymmetrical Exocyclic Dienones: Microwave‐Assisted Synthesis of Novel Mono‐ and Dispiropyrazoline Derivatives.
- Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction
- Design of novel dispirooxindolopyrrolidine and dispirooxindolopyrrolothiazole derivatives as potential antitubercular agents
- Synthesis of highly substituted spiropyrrolidines via 1, 3-dipolar cycloaddition reaction of N-metalated azomethine ylides. A new access to spiropyrrolines derivatives
- ChemInform Abstract: Synthesis of Novel Dispiropyrrolothiazoles by Three‐Component 1,3‐Dipolar Cycloaddition and Evaluation of Their Antimycobacterial Activity.
- A strategic approach to the synthesis of functionalized spirooxindole pyrrolidine derivatives: in vitro antibacterial, antifungal, antimalarial and antitubercular studies
- Synthesis of novel dispiropyrrolothiazoles by three-component 1,3-dipolar cycloaddition and evaluation of their antimycobacterial activity
- ÉTUDE DE LA RÉACTION DE CYCLOADDITION DIPOLAIRE-1,3 DES YLURES D'AZOMÉTHINE N-MÉTALLES SUR LES 3-ARYLIDÈNE-1-PHÉNYLPYRROLIDINE- 2,5-DIONES
- Synthesis, structure and luminescence properties of new spiro-heterocyclic pyrrolidine and 3,4-dihydro-3H-pyrrole derivative
- Regio- and Stereoselective 1,3-Dipolar Cycloaddition of C-Aryl-N-phenylnitrones over (E)-Arylidene-(2H)-indan-1-ones: Synthesis of Highly Substituted Novel Spiro-isoxazolidines
- 1,3-Dipolar cycloadditions of Arylcarbonitrile Oxides and Diaryl Nitrilimines with Some 2-Arylmethylene-1,3-Indanediones; regiochemistry of the Reactions
- 1,3‐Dipolar Cycloadditions of Arylcarbonitrile Oxides and Diaryl Nitrilimines with Some 2‐Arylmethylene‐1,3‐indanediones; Regiochemistry of the Reactions.
- Reaction of 2-Benzoyl-1,2-Dihydroisoquinoline-1-Carbonitrile Tetrafluoroborate Salt with 2-Arylmethylene-1,3-Indanediones. Regio- and Stereochemistry of the Reaction. Formation of Spiro Compounds
- Reaction of 2‐Benzoyl‐1,2‐dihydroisoquinoline‐1‐carbonitrile Tetrafluoroborate Salt with 2‐Arylmethylene‐1,3‐indanediones. Regio‐ and Stereochemistry of the Reaction. Formation of Spiro Compounds.
مجلات النشر
- ChemInform × 6
- Molecules × 4
- Journal of Molecular Structure × 3
- RSC Advances × 3
- Elsevier eBooks × 2
- The Journal of Organic Chemistry × 2
المنشورات حسب السنة
- 20262
- 20252
- 20246
- 20231
- 20223
- 20212
- 20202
- 20192
- 20164
- 20154
التعاون العلمي
المؤسسات الشريكة : Université de Sherbrooke · University of Sfax · Centre québécois sur les matériaux fonctionnels · Qassim University · University of Ha'il
بلدان المؤلفين المشاركين : كندا · فرنسا · السعودية
المؤلفون المشاركون
- Moheddine Askri
- Amani Toumi
- Khaled Hamden
- Saoussen Haddad
- Mohiedinne Askri
- Yoann Rousselin
- Michael Knorr
- Marek M. Kubicki
- Christopher Golz
- Carsten Strohmann B
- Chourouk Mhiri
- Rafik Gharbi
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
لماذا تختارون Dzcademia؟
ملفات أكاديمية ومقالات ومداخلات علمية: امنحوا أبحاثكم حضوراً عاماً منظماً. تساعد البيانات الوصفية المدمجة محركات البحث ومساعدات الذكاء الاصطناعي على التعرف على أعمالكم وفهم مراجعها.
علّق عبر Google
سجّل الدخول عبر Google للتعليق مباشرة على هذه الصفحة.