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  • 1
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Artificial intelligence. ; Internet of things. ; Electronic books.
    Description / Table of Contents: The book discusses the major contributions in the Edge AI domain of IoT systems: heterogeneous micro clusters employed for processing data and for exploiting adopted AI algorithms for the predictive analysis and or prescription.
    Type of Medium: Online Resource
    Pages: 1 online resource (347 pages)
    Edition: 1st ed.
    ISBN: 9781003825142
    Series Statement: Advances in Computational Collective Intelligence Series
    DDC: 006.3
    Language: English
    Note: Cover -- Half Title -- Series Information -- Title Page -- Copyright Page -- Table of Contents -- Preface -- Editors -- Abbreviations -- Part I Computational Intelligence: Edge AI Services -- Chapter 1 Edge Computational Intelligence: Fundamentals, Trends, and Applications -- 1.1 Introduction -- 1.2 Mainframe-Based Computing Model -- 1.3 PC File Server-Based Computing Model -- 1.4 C/S Architecture-Based Computing Model -- 1.5 Web and B/S Architecture-Based Computing Model -- 1.6 Mobile Devices-Centric Computing Model -- 1.7 Technologies-Based Computing Model -- 1.8 End-Edge-Cloud Computing Model -- 1.9 EC Trends -- 1.9.1 Heterogeneous Computing -- 1.9.2 Edge Intelligence (EI) -- 1.9.3 Edge Cloud Interface -- 1.9.4 5G + Edge Computing -- 1.10 EC Applications in Industry -- 1.10.1 Cloud Service Provider-Based Model -- 1.10.2 Site Facility Edge Service -- 1.10.3 Fixed Operator-Enabled EC Services -- 1.10.4 Mobile Operator-Centric EC Services -- 1.10.5 EC as a Self-Organizing Network -- 1.10.6 Near End Computing Services -- 1.11 Intelligent Edge (IE) and Edge Intelligence (EI) -- 1.11.1 Cost -- 1.11.2 Latency -- 1.11.3 Reliability -- 1.11.4 Privacy -- 1.12 Edge Computing -- 1.13 Edge AI & -- Its Need -- 1.14 Maturation of Neural Networks -- 1.15 Advancements in Computer Infrastructure -- 1.15.1 Use of IoT Devices -- 1.15.2 AI at the Edge: Requirement -- 1.15.3 Benefits of Cloud Computing and Edge Computing -- 1.16 Working of Edge AI -- 1.17 Advantages of Edge AI -- 1.17.1 Intelligence -- 1.17.2 Real-Time -- 1.17.3 Inexpensive -- 1.17.4 Improved Privacy -- 1.17.5 Abundancy -- 1.17.6 Persistency -- 1.17.7 Edge AI Future -- 1.18 Representative Applications of Edge AI -- 1.18.1 Smart Energy Forecasting -- 1.18.2 Predictive Analysis and Maintenance -- 1.18.3 AI-Driven Devices in Healthcare -- 1.18.4 Intelligent Virtual Assistants. , 1.18.5 Cloudlet and Micro-Data Centers -- 1.19 Fog Computing -- 1.20 Mobile Edge Computing -- 1.21 EC Terminologies -- 1.22 End-Edge-Cloud Computing -- 1.23 Hardware for EC -- 1.24 AI Hardware for EC -- 1.24.1 GPU-Enabled Hardware -- 1.24.2 Field Programmable Gate Array (FPGA)-Enabled Hardware [33, 34] -- 1.24.3 Integrated Circuit (ASIC)-Based Hardware -- 1.24.4 Potential of Integrated Commodities for Edge Nodes -- 1.25 EC Frameworks -- 1.25.1 Design Goals -- 1.25.2 End Users -- 1.25.3 Up-Scaling -- 1.25.4 System Characteristics -- 1.25.5 Application Environments -- 1.26 Edge Virtualization -- 1.26.1 Virtualization Strategies -- 1.26.2 Virtualizing Network -- 1.26.3 Network Slicing -- 1.26.4 Value Scenarios (VS) -- 1.26.5 Smart Parks -- 1.27 Video Surveillance -- 1.28 Industrial Internet of Things (IIoT) -- 1.29 Conclusion -- References -- Chapter 2 Securing IoT Services Using Artificial Intelligence in Edge Computing -- 2.1 Introduction -- 2.2 Conception and Depictions -- 2.2.1 IoT Service -- 2.2.2 Edge Computing -- 2.3 Framework of IoT Service With EC -- 2.3.1 Layer of Device -- 2.3.2 Layer of Network -- 2.3.3 Layer of Edge -- 2.3.4 Layer of Cloud -- 2.4 Privacy Maintenance With AI for Edge-Enabled IoT Services -- 2.4.1 Traditional Encryption Methods -- 2.4.1.1 Anonymization -- 2.4.1.2 Cryptographic Method -- 2.4.1.3 Data Obfuscation -- 2.4.2 AI-Based Privacy-Preserving Methods in ENs -- 2.4.2.1 CNN-Based Privacy Preservation -- 2.4.2.2 Privacy Preservation Using DNNs -- 2.5 Edge-Enabled IoT Services With AI and Blockchain -- 2.5.1 Blockchain for IoT Services' Security -- 2.5.1.1 Authentication Management and Access Control -- 2.5.1.2 Reliability and Confidentiality of Data -- 2.5.2 Blockchain for Edge-Enabled IoT Data Sharing -- 2.5.3 Blockchain for Edge-Enabled IoT Services' Efficiency -- 2.6 Challenges and Issues. , 2.6.1 Schemes Based On ML Security -- 2.6.2 Adopt ML in Blockchain Technology -- 2.7 Conclusions -- References -- Chapter 3 Computational-Based Edge AI Services and Challenges -- 3.1 Introduction -- 3.2 Background -- 3.3 Edge AI Services -- 3.3.1 Edge AI Services in Healthcare -- 3.3.2 Edge AI in Retail Industry -- 3.3.3 Role of Edge AI in Manufacturing Industry -- 3.3.4 Role of Edge AI in Transportation and Traffic Management -- 3.4 Edge Computing and AI Algorithms -- 3.4.1 Traditional Machine Learning -- 3.4.2 Deep Learning Algorithms -- 3.4.3 Reinforcement and Deep Reinforcement Learning -- 3.4.4 Evolutionary Algorithms -- 3.5 Challenges in Implementing Edge AI -- 3.6 Conclusion -- References -- Part II Computational Intelligence: Edge AI Security and Privacy -- Chapter 4 Security and Privacy in Edge AI: Challenges and Concerns -- 4.1 Introduction -- 4.1.1 IoT Service -- 4.1.2 IoT Architecture -- 4.1.2.1 Components of IoT Architecture -- 4.1.2.2 Layers of IoT Architecture -- 4.1.2.3 IoT Services -- 4.2 Edge Computing (EC) -- 4.3 EC in Consonance With IoT Devices -- 4.4 Edge AI -- 4.4.1 Definition -- 4.4.2 Traditional Intelligence Vs. Edge Intelligence -- 4.4.3 Need of Edge AI -- 4.4.4 Reasons for Deploying AI at the Edge -- 4.4.5 Pros of Edge AI -- 4.4.6 Working of Edge AI Technology -- 4.5 Edge AI Compared to Edge Computing -- 4.6 Security and Privacy Concerns for Edge AI -- 4.6.1 AI and Edge Computing Security -- 4.6.2 Integration of Edge Computing With AI -- 4.6.3 Security Risks of Edge Computing -- 4.6.3.1 Security in Edge Computing -- 4.6.3.2 Advantages of Security in Edge Computing -- 4.6.3.3 Security Strategies for Edge Computing -- 4.6.3.4 Edge Security Best Practices -- 4.6.3.5 Edge Security Vendors and Products -- 4.7 IoT Service Architecture With Edge Computing -- 4.7.1 Device Layer -- 4.7.2 Network Layer -- 4.7.3 Edge Layer. , 4.7.4 Cloud Layer -- 4.8 AI-Assisted Privacy Preservation for Edge-Enabled IoT Services -- 4.8.1 Traditional Encryption Methods -- 4.8.1.1 Anonymization -- 4.8.1.2 Cryptographic Method -- 4.8.1.3 Data Obfuscation -- 4.8.2 ENs With Lightweight AI Privacy-Preserving Methods -- 4.8.2.1 Role of CNNs in Privacy Preservation -- 4.8.2.2 Role of DNNs in Privacy Preservation -- 4.9 Edge-Enabled IoT Services By AI-Powered Blockchain -- 4.9.1 Role of Blockchain for Maintaining the Security of IoT Services -- 4.9.1.1 Access Control and Authentication Management -- 4.9.1.2 Confidentiality and Reliability of Data -- 4.9.2 Blockchain's Role in Edge-Enabled IoT Data Sharing -- 4.9.3 Enhancing Efficiency of Edge-Enabled IoT Services With Blockchain -- 4.10 Challenges and Concerns -- 4.10.1 Security Schemes Based On ML -- 4.10.1.1 High Cost of Communication and Computation -- 4.10.1.2 Security Techniques for Backup -- 4.10.2 Integration of ML and Blockchain Technology -- 4.11 Conclusion -- References -- Chapter 5 A Study of an Edge Computing-Enabled Metaverse Ecosystem -- 5.1 Introduction -- 5.1.1 Metaverse -- 5.1.2 Edge Computing -- 5.1.3 Edge Computing and Metaverse -- 5.1.3 Metaverse and Traditional Cloud-Based Platform -- 5.1.4 Edge Computing in the Metaverse -- 5.1.5 Use of Edge Computing By Prominent Leaders in Gaming Market -- 5.2 Relevance -- 5.3 Architectural Framework of an Edge Computing-Enabled -- 5.4 Edge Computing Case Studies in the Metaverse -- 5.5 Challenges for Edge Computing-Enabled Metaverse -- 5.5.1 Synchronization Challenges -- 5.5.2 Load Balancing -- 5.5.3 Network Complexities -- 5.5.4 Data Privacy and Security -- 5.5.5 Interoperability -- 5.5.6 Resource Constraints -- 5.5.7 Scalability -- 5.6 Conclusion -- References -- Chapter 6 Sustainable Communication-Efficient Edge AI: Algorithms and Systems -- 6.1 Introduction -- 6.1.1 Edge Devices. , 6.1.2 Cloud Computing -- 6.1.3 Challenges to Cloud Computing -- 6.1.4 Challenges Before Cloud Computing for Building Edge Computing -- 6.1.5 Edge Computing -- 6.1.6 Artificial Intelligence -- 6.1.7 Edge Computing With AI -- 6.1.8 Edge AI -- 6.2.1 Need of Edge AI -- 6.2.2 Advantages of Edge AI -- 6.2.3 How Does Edge AI Technology Work? -- 6.2.4 Edge AI Architecture -- 6.3 Communication-Efficient Edge AI: Algorithms and Systems -- 6.3.1 Communications-Efficient Algorithms for Edge AI -- 6.3.1.1 Federated Learning -- 6.3.1.2 Centralized Federated Learning -- 6.3.1.3 Centralized Federated Learning Design -- 6.4 Centralized Federated Learning Pseudo Code -- 6.4.1 Decentralized Federated Learning -- 6.4.2 Heterogeneous Dederated Learning -- 6.4.3 Quantization -- 6.4.4 Pruning -- 6.4.4.1 Design of Pruning -- 6.4.4.2 Pruning Techniques -- 6.4.4.5 Edge Intelligence Network -- 6.4.4.5 Edge-To-Edge Communication -- References -- Part III Computational Intelligence: Edge Computing and AI Applications -- Chapter 7 Machine Learning-Based Hybrid Technique for Securing Edge Computing -- 7.1 Introduction -- 7.2 Literature Review -- 7.2.1 Static Analysis Based On Malware Detection -- 7.2.2 Dynamic Analysis Based On Malware Detection -- 7.2.3 Hybrid Malware Analysis Techniques -- 7.3 Proposed Hybrid Malware Analysis -- 7.3.1 HybriDroid Architecture -- 7.3.2 Classifier Training for HybriDroid and CHybriDroid -- 7.4 Experimental Results -- 7.4.1 Data Set -- 7.4.2 Feature Selection -- 7.4.3 Feature Ranking -- 7.4.4 Result Discussion -- 7.4.5 Prediction Model Overhead -- 7.4.6 Analysis -- 7.5 Conclusion and Future Work -- References -- Chapter 8 A Study of Secure Deployment of Mobile Services in Edge Computing -- 8.1 Introduction -- 8.1.1 MEC Service Deployment -- 8.1.2 Computation Offloading -- 8.1.3 Data Placement -- 8.2 Basic Concepts and Definitions. , 8.2.1 Service Deployment.
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  • 2
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Electronic books.
    Description / Table of Contents: This edited volume reports the latest developments in practical and selective reactions and methods involving carbenes and nitrenes and provides details of the structural diversity of heterocycles.
    Type of Medium: Online Resource
    Pages: 1 online resource (415 pages)
    Edition: 1st ed.
    ISBN: 9781837674855
    DDC: 547.59
    Language: English
    Note: Cover -- Synthesis, Properties, and Biological Applications of  1,3-Thiazoles -- 1.1 Introduction -- 1.2 Recent Advances in the Synthesis of Thiazole -- 1.3 Biological Applications -- 1.3.1 Thiazole as an Anticancer Agent -- 1.3.2 Thiazole as an Antioxidant Agent -- 1.3.3 Thiazole as an Antitubercular Agent -- 1.3.4 Thiazole as an Antimicrobial Agent -- 1.4 Conclusion -- Abbreviations -- References -- Synthesis, Properties, and Therapeutic Applications of Dithiazoles -- 2.1 Introduction -- 2.2 Synthesis and Chemistry -- 2.2.1 Reaction at the More Reactive C-5 Position of Appel's Salt -- 2.2.2  Reaction at the Less Reactive C-4 Position of Appel's Salt -- 2.2.3 Synthesis of Fused Dithiazoles -- 2.3 Biological Activity of 1,2,3-Dithiazoles -- 2.3.1 Antimicrobial Activities of 1,2,3-Dithiazoles -- 2.3.2 Antiviral Activities of 1,2,3-Dithiazoles -- 2.3.3 Anticancer Activities of 1,2,3-Dithiazoles -- 2.3.4 Other Biological Activities -- 2.4 Conclusion -- References -- Isothiazoles: Synthetic Strategies and Pharmacological Applications -- 3.1 Introduction -- 3.2 Recent Advances in the Synthesis of Isothiazoles -- 3.3 Biological Applications -- 3.3.1 Isothiazole as the Anticancer Agent -- 3.3.2 Isothiazole as the Antidiabetic Agent -- 3.3.3 Isothiazole as an Antiviral Agent -- 3.3.4 Isothiazole with Neurological Activity -- 3.3.5 Isothiazole as Antimicrobial/Antibacterial/Antifungal Agents -- 3.3.6 Isothiazole as Fungicides/Pesticides/Plant Protectors -- 3.4 Conclusion -- Abbreviations -- References -- Synthesis, Properties, and Biological Applications of Benzothiazoles -- 4.1 Introduction -- 4.2 Synthesis of Benzothiazoles and Their Derivatives -- 4.2.1 Synthesis from Isothiocyanates -- 4.2.2 Synthesis from Triethyl Orthoformate -- 4.2.3 Synthesis from Aniline Derivatives -- 4.2.4 Synthesis from Hydrazine. , 4.2.5 Intramolecular Formation of C-S Using Pd and Cu Catalysts -- 4.2.6 Solvent-free Synthesis -- 4.2.7 Cyclization -- 4.2.8 One-pot Synthesis of 2-Aminobenzothiazoles -- 4.2.9 Synthesis by Suzuki-Miyaura -- 4.2.10 Fused Benzothiazole Synthesis -- 4.3 Physicochemical Properties of Benzothiazoles -- 4.4 Biological Activities of Benzothiazoles -- 4.4.1 Antimicrobial Activity -- 4.4.2 Anticancer Activity -- 4.4.3 Anti-inflammatory Effects -- 4.4.4 Antiviral Activity -- 4.4.5 Antidiabetic Activity -- 4.4.6 Antioxidant Activity -- 4.4.7 Antitubercular Activity -- 4.5 Emerging Trends and Future Prospects -- 4.6 Conclusion -- Synthesis, Properties, and Biological Applications of 2,4-Thiazolidinediones -- 5.1 Introduction -- 5.1.1 Importance of 2,4-Thiazolidinedione Analogues in Medicinal Chemistry -- 5.2 Recent Advances in Synthesis -- 5.3 Medicinal Chemistry Applications -- 5.3.1 Antidiabetic Effects -- 5.3.2 Anticancer Effects -- 5.3.3 Anti-inflammatory Effects -- 5.3.4 Antioxidant Effects -- 5.4 TZDs and Their Side Effects -- 5.5 Conclusion -- Abbreviations -- References -- Synthesis, Properties, and Biological Applications of  1,2,4-Thiadiazoles -- 6.1 Introduction -- 6.2 Recent Advances in the Synthesis of 1,2,4-Thiadiazoles -- 6.3 Biological Applications -- 6.3.1 Anticonvulsant Activity -- 6.3.2 Anticancer Activity -- 6.3.3 Central Nervous System Activity -- 6.3.4 Cathepsin B Inhibitor -- 6.3.5 Anticholinesterase Activity and Antioxidant Properties -- 6.3.6 Alzheimer's Disease -- 6.3.7 Anticonvulsant Activity -- 6.3.8 Plant Growth Regulator Herbicide -- 6.4 Conclusion -- Abbreviations -- Acknowledgements -- References -- Synthesis, Properties, and Biological Applications of 1,3,4-Thiadiazoles -- 7.1 Introduction -- 7.1.1 Isomers of Thiadiazoles -- 7.1.2 Chemical Properties and Characteristics of 1,3,4-Thiadiazoles. , 7.2 Synthesis of 1,3,4-Thiadiazoles -- 7.2.1 Conventional Methods for the Synthesis of 1,3,4-Thiadiazoles -- 7.2.2 Green Methods for the Synthesis of 1,3,4-Thiadiazoles -- 7.3 Applications of 1,3,4-Thiadiazoles in Currently Marketed Drugs/Investigational Compounds -- 7.4 Biological Activities of 1,3,4-Thiadiazoles -- 7.4.1 Anti-inflammatory Agents -- 7.4.2 Anti-diabetic Agents -- 7.4.3 Anti-seizure/Anti-epileptic/Anti-convulsant Agents -- 7.4.4 Anti-cancer Agents -- 7.4.5 Anti-Alzheimer Agents -- 7.4.6 Anti-viral Agents -- 7.4.7 Anti-tuberculosis Agents -- 7.4.8 Antimicrobial Agents -- 7.4.9 Diuretic Agents -- 7.4.10 Anti-obesity Agents -- 7.4.11 Anti-glaucoma Agents -- 7.4.12 Anti-platelet Agents -- 7.4.13 Anti-aging Agents -- 7.4.14 Anti-leishmanicidal Agents -- 7.4.15 Anti-H. pylori Agents -- 7.4.16 Anti-fungal Agents -- 7.5 Patent Updates on 1,3,4-Thiadiazoles -- 7.6 Ongoing Clinical Trials -- Synthesis, Properties, and Biological Applications of Thiopyrans -- 8.1 Introduction -- 8.2 Developments in the Synthesis of Thiopyran Derivatives -- 8.2.1 Synthesis of Thiopyran Derivatives Using Glutaraldehyde Derivatives -- 8.2.2 Synthesis of Thiopyrans from Thioenolates -- 8.2.3 Synthesis of Thiopyrans from Thioamides -- 8.2.4 Hantzsch-like Synthesis of 4H-thiopyrans -- 8.2.5 Synthesis of Thiopyrans from Acetylenes -- 8.2.6 Synthesis of Thiopyrans from Enamines -- 8.2.7 Synthesis of Thiopyrans from Thiopyrylium Salts -- 8.2.8 Synthesis of Thiopyrans by Reduction -- 8.2.9 Synthesis of Thiopyrans by Reactions with C-nucleophiles and Reductive C-substitutions -- 8.2.10 Reactions with Oxygen and Sulfur Nucleophiles -- 8.2.11 Synthesis of Thiopyrans by Reactions with Nitrogen and Phosphorus Nucleophiles -- 8.2.12 Synthesis of Thiopyrans from Thiopyrones and Similar Cyclic Ketones -- 8.2.13 Synthesis of Thiopyrans from Thiophenes. , 8.2.14 Synthesis of Thiopyrans from 1,5-Diketones -- 8.2.15 Synthesis of Thiopyrans by Electrosynthesis and with Catalysts -- 8.2.16 Synthesis of Thiopyrans from β-Keto Esters -- 8.2.17 Synthesis of Thiopyrans from N-methylisatin -- 8.2.18 Synthesis of Thiopyrans by Intramolecular Coupling -- 8.3 Pharmacological Profile of Thiopyran Derivatives -- 8.3.1 Antibacterial and Antifungal Activities -- 8.3.2 Anticancer Activity -- 8.3.3 Antiviral Activity -- 8.3.4 VEGFR-2 Inhibitory Activity -- 8.3.5 5-LOX Inhibitory Activity -- 8.3.6 Larvicidal Activity -- 8.3.7 Nematicidal Activity -- 8.3.8 Anti-inflammatory Activity -- 8.3.9 Hypoglycemic Activity -- 8.4 Conclusion -- Recent Developments in the Synthesis and Biological Applications of Thiazine -- 9.1 Introduction -- 9.2 Recent Advances in the Synthesis of Thiazine -- 9.3 Biological Applications -- 9.3.1 Thiazine as Anticancer Agents -- 9.3.2 Thiazine as Antimicrobial Agents -- 9.3.3 Thiazine as Antitubercular Agents -- 9.3.4 Thiazine as Anticonvulsant Agents -- 9.3.5 Thiazine as Antihypertensive Agents -- 9.3.6 Thiazine as Miscellaneous Agents -- 9.4 Conclusions -- Synthesis, Properties, and Biological Applications of Benzothiazepines -- 10.1 Introduction -- 10.2 Synthetic Approaches for Benzothiazepine -- 10.3 Synthesis of 1,4-Benzothiazepine -- 10.3.1 Synthesis of 4,1-Benzothiazepine-4-oxide 10.3.29 -- 10.3.2 Synthesis of 4,1-Benzothiazepine-4,4-dioxide 10.3.30 -- 10.3.3 Synthesis of 1,5-Dihydro-4,1-benzothiazepine Derivatives 10.3.31 -- 10.3.4 Reaction Mechanism -- 10.3.5 Synthesis of 2,3,4,5-Tetrahydrobenzo[1,4]thiazepines via N-Acyliminium Cyclization36 -- 10.3.6 Synthesis of Phosphonomethylbenzothiazepine29 -- 10.3.7 Asymmetric Reduction of 10.3.45 and Conversion into ASBT Inhibitor 10.3.48 -- 10.3.8 Synthesis of 1,4-Benzothiazepines from Cyclic Sulfenamides37. , 10.3.9 Synthesis of 1,4-Benzothiazepine using Cysteine38 -- 10.3.10 Synthesis of Bicyclic 1,4-Benzothiazepines39 -- 10.4 Biological Behavior of 1,4-Benzothiazepines -- 10.4.1 Anti-tumor potential -- 10.4.2 Anti-malarial potential -- 10.4.3 Anti-bacterial potential -- 10.4.4 Anti-fungal potential -- 10.4.5 Anti-diabetic Potential -- 10.4.6 Antioxidant Potential -- 10.4.7 Analgesic and Anti-inflammatory Potential -- 10.4.8 Anti-convulsant Potential -- 10.4.9 Other Biological Potentials -- 10.5 Structure-Activity Relationship Study -- 10.6 Conclusion -- Synthesis, Properties, and Biological Applications of Thiophene -- 11.1 Introduction -- 11.2 Recent Developments in the Synthesis of Thiophene Derivatives -- 11.2.1 Synthesis of Thiophene Derivatives Through Metal-catalyzed Reaction -- 11.2.2 Synthesis of Thiophene Derivatives Through Iodocyclization Reaction -- 11.2.3 Synthesis of Thiophene Derivatives Through Metal-free Approaches -- 11.2.4 Synthesis of Thiophene Derivatives Through Multicomponent Reaction Approaches -- 11.3 Recent Advances in Biological Applications of Thiophene Derivatives -- 11.3.1 Antimicrobial Activity of Thiophene Derivatives -- 11.3.2 Antileishmanial Activity of Thiophene Derivatives -- 11.3.3 Antiviral Activity of Thiophene Derivatives -- 11.3.4 Anticancer Activity of Thiophene Derivatives -- 11.3.5 Anti-inflammatory Activity of Thiophene Derivatives -- 11.3.6 Anticonvulsant and Antiurease Activity of Thiophene Derivatives -- 11.3.7 Antioxidant, Enzyme Inhibition, and Antithrombotic Activity of Thiophene Derivatives -- Synthesis, Properties, and Biological Applications of Benzothiophene -- 12.1 Introduction -- 12.1.1 Physical Properties -- 12.2 Recent Synthesis -- 12.2.1 Cyclization Reactions by Lewis Acid -- 12.2.2 Cyclization Reactions by Halogen Catalysis -- 12.2.3 Cyclization Reactions by Transition Metal Catalysis. , 12.2.4 Cyclization Reactions by Base Catalysis.
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  • 3
    Online Resource
    Online Resource
    Cham : Springer Nature Switzerland | Cham : Imprint: Springer
    Keywords: Sustainability. ; Environmental management. ; Ecology .
    Description / Table of Contents: Chapter 1.Editorial: Global Sustainability: Trends, Challenges, and Case studies -- Part I. Global Sustainability: Trends -- Chapter 2. Emerging Trends in Sustainability: A Conceptual Exploration (Anitha. K) -- Chapter 3. Sustainable Solutions to Combat Soil Erosion Using Biogenic Agents (Evangelin Ramani Sujatha) -- Chapter 4. Circular Economy for Sustainable Development in India (Vijai) -- Chapter 5. Evaluation of Sustainability Practices in Higher Education: A Study on Assessment Tools GASU and AISHE (Parvez Ahmad) -- Part II. Global Sustainability: Challenges -- Chapter 6. Soil Conservation for Global Sustainability (Prasann Kumar) -- Chapter 7. Designing a Framework for Sustainable Supply Chain Management of Coal Transportation (Suchismita Satapathy) -- Chapter 8. Workplace Wellbeing of LGBT Individuals: Impact on Sustainability (Vaishnavi Nambiar) -- Part III. Global Sustainability: Case Studies -- Chapter 9. Impact of Urban Expansion onUrban Heat: A Case Study of Greater London (Semudara, Oluwaseun Moses) -- Chapter 10. Sustainable Cassava: A Case Study of Global Sustainability (Shrikaant Kulkarni) -- Chapter 11. Case Studies in Sustainable Business Management in India (Amit Kumar Marwah) -- Chapter 12. Role of Agricultural Science Centres in attaining Sustainability in India: A Case Study (A. K. Wavare) -- Chapter 13. Collective Action for Transformative Change: The Case of Helston Climate Action Group (UK) (Kolade Victor Otokiti).
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource(XVI, 293 p. 56 illus., 28 illus. in color.)
    Edition: 1st ed. 2024.
    ISBN: 9783031574566
    Series Statement: World Sustainability Series
    Language: English
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  • 4
    Online Resource
    Online Resource
    Singapore : Springer Nature Singapore | Singapore : Imprint: Springer
    Keywords: Medicine ; Biology ; Drug delivery systems. ; Genetics ; Imaging systems in biology. ; Biology
    Description / Table of Contents: Chapter 1. Editorial: Biosystems -- 2. Potential of Biotechnology in cancer management -- 3. Biosimilars: Promising and Rapidly Emerging Biotherapeutics -- 4. Applications of Nanomaterials in Medicine: Current status and future scope -- 5. Biomedical Applications of Nanofluids in Drug Delivery.
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource(XX, 289 p. 58 illus., 48 illus. in color.)
    Edition: 1st ed. 2023.
    ISBN: 9789819952816
    Language: English
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