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ویرایش:
نویسندگان: Ameta K.L.
سری:
ISBN (شابک) : 9789819743070
ناشر: Springer
سال نشر: 2024
تعداد صفحات: 350
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 18 مگابایت
در صورت تبدیل فایل کتاب S-Heterocycles: Synthesis and Biological Evaluation به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب S-Heterocycles: سنتز و ارزیابی بیولوژیکی نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
Cover Half Title S-Heterocycles: Synthesis and Biological Evaluation Copyright Foreword Preface Contents Editor and Contributors 1. Synthesis and Biological Evaluation of Thiophene and Its Derivatives 1.1 Introduction 1.2 General Approaches to Thiophene Ring Synthesis 1.3 Biological Activities of Thiopene Molecules 1.3.1 Anti-inflammatory Activity 1.3.2 Anticancer Activity 1.3.3 Antioxidant Activity 1.3.4 Antimicrobial Activity 1.4 Conclusion References 2. Synthesis and Biological Evaluation of 4-Thiazolidinone Scaffold: A Versatile Chemistry and Diverse Biological Applications in the Drug Discovery and Development 2.1 Introduction 2.2 Synthesis of Thiazolidinone 2.3 Pharmaceutical Profile of Thiazolidinones 2.3.1 Antimicrobial Activity 2.3.2 Anticancer Activity 2.3.3 Antimalarial Activity 2.3.4 Anti-inflammatory Activity 2.3.5 Anti-HIV Activity 2.3.6 Antitubercular Activity 2.3.7 Antidiabetic Activity 2.3.8 Antioxidants Activity 2.3.9 Antiparasitic Activity 2.3.10 Miscellaneous Activity 2.4 Conclusion References 3. Synthesis and Biological Evaluation of Thiazoline, Thiophene and Thiazole Scaffolds 3.1 Introduction 3.2 Thiazoline Derivatives 3.3 Thiophene 3.4 Thiazole Derivatives 3.5 Biological Claim of Thiazole Scoffed 3.6 Anticancer Activity 3.7 Anticonvulsant Activity 3.8 Antitubercular Activity 3.9 Anti-inflammatory Activity 3.10 Conclusion References 4. Synthesis and Biological Evaluation of Thiirane and Its Derivatives 4.1 Introduction 4.2 Synthesis of Thiirane 4.2.1 Derivatives of Thiirane 4.3 Conclusion References 5. Synthesis and Biological Evaluation of 1,3,5-Dithiazinanes: Synthesis, Stereochemistry and Applications 5.1 Introduction 5.2 Multicomponent Cyclothiomethylation of Amines as a Methodology for the Synthesis of 1,3,5-Dithiazinanes 5.3 Recyclization of 1,3,5-Hexahydrotriazines in the Synthesis of 1,3,5-Dithiazinanes 5.4 1,3,5-Dithiazinanes as S,N-Containing Polydentate Ligands 5.4.1 Complexation with Lewis Acids 5.4.2 Complexation with [H2Os3(CO)10] 5.4.3 Complexes with Alkyl Halides 5.5 Synthesis of Organoelement Derivatives of 1,3,5-Dithiazinanes 5.6 C2 Functionalization of 1,3,5-Dithiazinanes 5.7 Original Approaches to the Synthesis of 1,3,5-Dithiazinanes 5.8 Practical Application of 1,3,5-Dithiazinanes 5.9 Conclusion References 6. Synthesis and Biological Evaluation of Benzothiazepine, Benzothiazole, and Benzothiophene Derivatives 6.1 Introduction 6.2 Benzothiazepines 6.2.1 Different Synthetic Approach for Benzothiazepines 6.3 Benzothiazole 6.3.1 Different Synthetic Approach for Benzothiazole Derivatives 6.4 Benzothiophene 6.4.1 Different Synthetic Approach for Benzothiophene Derivatives 6.5 Conclusion References 7. Synthesis and Biological Evaluation of Some Fused Pyrrolothiazoles, Pyrazolothiazoles, and Imidazothiazoles 7.1 Introduction 7.2 Synthesis of Pyrrolothiazole 7.3 Synthesis of Pyrazolothiazoles 7.3.1 Synthesis of Pyrazolo[3,4-d]thiazoles 7.3.2 Synthesis of Pyrazolo[4,3-d]thiazoles 7.3.3 Synthesis of Pyrazolo[5,1-d]thiazoles 7.3.4 Synthesis of Imidazothiazole 7.3.5 Conclusion References 8. Synthesis and Biological Evaluation of Some Dithiazines 8.1 Introduction 8.2 Synthesis and Biological Activity 8.3 Conclusion References 9. Synthesis and Biological Evaluation of Some Sulfur-Containing Spiro Compounds 9.1 Introduction 9.2 Construction of Five-Member Sulfur-Containing Rings 9.2.1 Construction of Thiophene Ring Annulated Spiro Compounds 9.2.2 Construction of Dithiolane Ring Annulated Spiro Compounds 9.3 Construction of Six-Member Sulfur-Containing Rings 9.3.1 Construction of Thiopyran Ring Annulated Spiro Compounds 9.3.2 Construction of Dithiine Ring Annulated Spiro Compounds 9.4 Conclusion References 10. Synthesis and Biological Evaluation of Some Polycyclic Aromatic Hydrocarbons 10.1 Benzothiophene 10.1.1 Introduction 10.2 Synthesis 10.2.1 Biological Activity 10.2.2 Conclusion 10.3 Dibenzothiophene 10.3.1 Introduction 10.3.2 Synthesis 10.3.3 C-X Cleavage for Dibenzothiophene Synthesis 10.3.4 Conclusion 10.4 Thienothiophene 10.4.1 Introduction 10.4.2 Synthesis 10.4.3 Biological Activity 10.4.4 Conclusion References 11. Synthesis and Biological Evaluation of Some Thietane Derivatives 11.1 General Introduction of Thietanes and Its Derivatives 11.2 Synthetic Routes for Thietanes and Its Derivatives 11.3 Biological Potency of Thietanes and Its Derivatives 11.3.1 Anti-depressant and Anti-hypotensive Activity 11.3.2 Anti-cancer Activity 11.3.3 Anti-viral Activity 11.3.4 Anti-bacterial and Anti-infection Activity 11.3.5 Anti-tuberculosis Activity 11.3.6 Anti-inflammation Activity 11.3.7 Anti-diabetic Activity 11.3.8 Anti-platelet and Anti-coagulant Activity 11.4 Conclusion References 12. Synthesis and Biological Evaluation of Fused Thiazolotriazole and Imidazothiadiazole Scaffolds 12.1 Introduction 12.2 Thiazolotriazoles 12.2.1 Introduction 12.2.2 Synthesis of Thiazolotriazoles 12.2.3 Biological Activity 12.3 Imidazothiadiazole 12.3.1 Introduction 12.3.2 Synthesis of Imidazothiadiazole 12.3.3 Biological Activity of Imidazo[2,1-b][1,3,4]Thiadiazole 12.4 Miscellaneous Reaction 12.4.1 Pyrrolo[2,1-b]thiazole 12.4.2 Imidazotriazoles 12.5 Conclusion References