03943nam 22006855 450 991072895210332120230602134446.03-031-34851-610.1007/978-3-031-34851-8(MiAaPQ)EBC30564795(Au-PeEL)EBL30564795(OCoLC)1381477858(DE-He213)978-3-031-34851-8(BIP)091896401(PPN)27226279X(CKB)26821653100041(EXLCZ)992682165310004120230602d2023 u| 0engurcnu||||||||txtrdacontentcrdamediacrrdacarrierWireless and Satellite Systems 13th EAI International Conference, WiSATS 2022, Virtual Event, Singapore, March 12-13, 2023, Proceedings /edited by Jun Zhao1st ed. 2023.Cham :Springer Nature Switzerland :Imprint: Springer,2023.1 online resource (135 pages)Lecture Notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering,1867-822X ;509Print version: Zhao, Jun Wireless and Satellite Systems Cham : Springer,c2023 9783031348501 Security and Privacy in Healthcare, Transportation, and Satellite Networks -- TF-Net: Deep Learning Empowered Tiny Feature Network for Night-time UAV Detection -- Study on detection of vascular inner wall with IVUS image -- Anomaly Detection for Connected Autonomous Vehicles using LSTM and Gaussian Naïve Bayes -- Detection Algorithms based on eigenvalues of sampling Covariance Matrix for Satellite Cognitive Network -- Advanced Technologies in Wireless Communication Systems -- Hybrid Beamforming Design for Multi-User Multi-Stream Communications with Terahertz Massive MIMO -- Photovoltaic Devices Design Based on Simultaneous Visible-light Information and Power Transfer Circuits -- Marketing in Wireless Communication: A Systematic Review -- A robust beamforming algorithm for satellite communication -- Network Efficiency and Reliability -- Average Age of Incorrect Information in Random Access Channels for IoT Systems.This book constitutes the refereed post-conference proceedings of the 13th International Conference on Wireless and Satellite Services, WiSATS 2022, held in March 12-13, 2023. Due to COVID-19 pandemic the conference was held virtually. The 9 full papers were carefully reviewed and selected from 23 submissions. They were organized in topical sections as follows: Security and Privacy in Healthcare, Transportation, and Satellite Networks, Advanced Technologies in Wireless Communication Systems, Network Efficiency and Reliability.Lecture Notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering,1867-822X ;509Computer networksApplication softwareArtificial intelligenceComputer networks—Security measuresComputer Communication NetworksComputer and Information Systems ApplicationsArtificial IntelligenceMobile and Network SecurityEngineeringTechnology & EngineeringComputer networks.Application software.Artificial intelligence.Computer networks—Security measures.Computer Communication Networks.Computer and Information Systems Applications.Artificial Intelligence.Mobile and Network Security.621.384Zhao Jun989096Zhao JunedtMiAaPQMiAaPQMiAaPQBOOK9910728952103321Wireless and Satellite Systems3384495UNINA05263nam 2200673Ia 450 991102033220332120200520144314.09786612461071978128246107912824610799780470747957047074795197804707479330470747935(CKB)1000000000822301(EBL)470758(OCoLC)476311784(SSID)ssj0000336424(PQKBManifestationID)11229534(PQKBTitleCode)TC0000336424(PQKBWorkID)10281868(PQKB)10465452(MiAaPQ)EBC470758(Perlego)2756899(EXLCZ)99100000000082230120090827d2009 uy 0engur|n|---|||||txtccrCumulenes in click reactions /Henri UlrichHoboken, NJ Wiley20091 online resource (566 p.)Description based upon print version of record.9780470779323 0470779322 Includes bibliographical references and index.Cumulenes in Click Reactions; Contents; Preface; Acknowledgements; 1 General Introduction; References; 2 1-Carbon Cumulenes; 2.1 Sulfines, R2C SO; 2.1.1 Introduction; 2.1.2 Dimerization Reactions; 2.1.3 Cycloaddition Reactions; References; 2.2 Sulfenes, R2C S(O)O; 2.2.1 Introduction; 2.2.2 Dimerization Reactions; 2.2.3 Cycloaddition Reactions; References; 2.3 Other 1-Carbon Cumulenes; 2.3.1 Thiocarbonyl S-Imides; 2.3.2 Thiocarbonyl S-Sulfides; 2.3.3 1-Aza-2-azoniaallene Salts; References; 3 2-Carbon Cumulenes; 3.1 Carbon Oxides, O C O, :CO; 3.1.1 Introduction; 3.1.2 Cycloaddition Reactions3.1.3 Insertion ReactionsReferences; 3.2 Carbon Sulfides, S C S, S CO; 3.2.1 Introduction; 3.2.2 Cycloaddition Reactions; 3.2.3 Insertion Reactions; References; 3.3 Carbon Nitrides; 3.3.1 Isocyanates, RN CO; References; 3.3.2 Isothiocyanates, RN C S; References; 3.3.3 Carbodiimides, RN C NR; References; 3.4 Center Carbon Phosphorallenes, P C P; 3.4.1 Introduction; 3.4.2 Dimerization Reactions; 3.4.3 Cycloaddition Reactions; References; 4 1,2-Dicarbon Cumulenes; 4.1 Ketenes, R2C C O; 4.1.1 Introduction; 4.1.2 Dimerization Reactions; 4.1.3 Trimerization Reactions; 4.1.4 Cycloaddition ReactionsReferences4.2 Thioketenes, R2C C S; 4.2.1 Introduction; 4.2.2 Dimerization Reactions; 4.2.3 Cycloaddition Reactions; References; 4.3 Ketenimines, R2C C NR; 4.3.1 Introduction; 4.3.2 Dimerization Reactions; 4.3.3 Cycloaddition Reactions; References; 4.4 1-Silaallenes, R2C C Si; 4.4.1 Introduction; 4.4.2 Dimerization Reactions; 4.4.3 Cycloaddition Reactions; References; 4.5 1-Phosphaallenes, R2C C P; 4.5.1 Introduction; 4.5.2 Dimerization Reactions; 4.5.3 Cycloaddition Reactions; References; 4.6 Other Metal Allenes; 4.6.1 Introduction; 4.6.2 Cycloaddition Reactions; References5 1,3-Dicarbon Cumulenes5.1 Thiocarbonyl S-ylides, R2C S CH2; 5.2 2-Azaallenium Salts, R2C N+ CR2; 5.3 1-Oxa-3-azoniabutatriene Salts, R2C N+ C O; 5.4 1-Thia-3-azabutatriene Salts, R2C N+ C S; 5.5 Phosphorus Ylides; References; 6 1,2,3-Tricarbon Cumulenes; 6.1 Allenes, R2C C CR2; 6.1.1 Introduction; 6.1.2 Dimerization Reactions; 6.1.3 Oligomerization Reactions; 6.1.4 Cycloaddition Reactions; References; 6.2 [3] Cumulenes, R2C C C CR2; 6.2.1 Introduction; 6.2.2 Dimerization Reactions; 6.2.3 Trimerization Reactions; 6.2.4 Cycloaddition Reactions; References; 6.3 [4] Cumulenes, R2C C C C CR26.3.1 Introduction6.3.2 Dimerization Reactions; 6.3.3 Cycloaddition Reactions; References; 6.4 [5] Cumulenes, R2C C C C C CR2; 6.4.1 Introduction; 6.4.2 Dimerization Reactions; 6.4.3 Cycloaddition Reactions; References; 7 Noncarbon Cumulenes; 7.1 Azides, RN N N; 7.1.1 Introduction; 7.1.2 Oligomers; 7.1.3 [3+2] Cycloaddition Reactions; References; 7.1.4 Some Applications in Modifications of Biopolymers; Application References; 7.2 Triazaallenium Salts, RN N+ NR; 7.2.1 Introduction; 7.2.2 Cycloaddition Reactions; References; 7.3 Sulfur Oxides; 7.3.1 Introduction; 7.3.2 Sulfur Dioxide, O S O7.3.3 Sulfur Trioxide, O SO2Cumulenes are organic molecules with two or more cumulative (consecutive) double bonds. Their reactions often proceed at room temperature, with or without a catalyst, and are stereospecific, giving the reaction products in high yields - features characteristic of "click reactions". Cumulenes in Click Reactions presents a comprehensive list of cumulene systems and their reactions, with an emphasis on their "click-like" nature. The chapters are structured according to the number of carbon atoms in the system, including coverage of: introduction to the chemistAlkenesChemical reactionsAlkenes.Chemical reactions.547.2547.412Ulrich Henri1925-1658044MiAaPQMiAaPQMiAaPQBOOK9911020332203321Cumulenes in click reactions4417654UNINA