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Titlebook: Click Chemistry; Vinod K. Tiwari,Manoj K. Jaiswal,Sumit K. Singh Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusiv

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樓主
發(fā)表于 2025-3-21 19:25:25 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Click Chemistry
編輯Vinod K. Tiwari,Manoj K. Jaiswal,Sumit K. Singh
視頻videohttp://file.papertrans.cn/243/242141/242141.mp4
概述Covers the topics of ‘Click Chemistry’ and ‘Bioorthogonal Chemistry’.Brings together the fundamental and applied aspects of click chemistry.Discusses applications ranging from chemical biology to cata
叢書名稱Materials Horizons: From Nature to Nanomaterials
圖書封面Titlebook: Click Chemistry;  Vinod K. Tiwari,Manoj K. Jaiswal,Sumit K. Singh Book 2024 The Editor(s) (if applicable) and The Author(s), under exclusiv
描述.This book comprehensively covers the fundamentals and latest advancements in the area of click chemistry. It discusses notable applications of click chemistry in various emerging areas ranging from chemical biology to catalysis and from medicinal chemistry to material sciences. Various topics covered in this book are catalysis in regioselectivity in click chemistry, organocatalysis in triazole synthesis, Bertozzi’s Bioorthogonal Concept, photo-triggered click chemistry, SuFFEx Click, Thiol-Ene Click, MCR Click, Intramolecular Click Chemistry, synthesis of diverse triazoles and their applications, Click‘s Post Functionalization, etc. The book is a valuable reference for beginners, researchers and professionals interested in sustainable click concept and its diverse applications in allied fields..
出版日期Book 2024
關(guān)鍵詞Bioothogonal Chemistry; RuAAC; Azides; Alkynes; Biomolecules; Cyclization; CuAAC; Regioselectivity; Carbohyd
版次1
doihttps://doi.org/10.1007/978-981-97-4596-8
isbn_softcover978-981-97-4598-2
isbn_ebook978-981-97-4596-8Series ISSN 2524-5384 Series E-ISSN 2524-5392
issn_series 2524-5384
copyrightThe Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Singapor
The information of publication is updating

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發(fā)表于 2025-3-22 00:04:20 | 只看該作者
,CuAAC ‘Click Chemistry’-Mediated Synthesis of 1,4-Disubstituted 1,2,3-Triazoles,oles with great ease. This modular tool stands out due to its exceptional efficiency, regioselectivity, and mild reaction conditions and is thus considered one of the most versatile organic reactions investigated so far. The versatility of CuAAC is well demonstrated through its application in divers
板凳
發(fā)表于 2025-3-22 00:42:20 | 只看該作者
地板
發(fā)表于 2025-3-22 06:32:42 | 只看該作者
Organocatalyzed 1,2,3-Triazoles Forming Click Chemistry,s. Traditional methods for triazole formation often rely on metal catalysts, which can be expensive and environmentally unfriendly. This chapter explores the synthesis of 1,2,3-triazoles through click chemistry facilitated by organocatalysis. This chapter highlights the use of an efficient and eco-f
5#
發(fā)表于 2025-3-22 10:15:18 | 只看該作者
Catalyst-Free Thermally Induced 1,2,3-Triazole Forming Approaches, not only simplifies the synthetic procedure but also aligns with the principles of green chemistry, reducing the environmental footprint. Comprehensive mechanistic studies reveal the role of thermal energy in facilitating the cycloaddition process, providing insights into reaction kinetics and sele
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發(fā)表于 2025-3-22 14:13:40 | 只看該作者
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發(fā)表于 2025-3-23 06:18:58 | 只看該作者
Click Chemistry in Dendrimer Synthesis,mers due to its high efficiency, selectivity, and mild reaction conditions. Dendrimers are highly branched macromolecules with precise and controllable architectures and through benefit from CuAAC‘s ability to form stable 1,2,3-triazole linkages, they enable the generation of uniform and well-define
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