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

潰爛

Click Chemistry in Polymer Science,cks under mild conditions with high yields and minimal by-products. CuAAC ‘Click chemistry’ has revolutionized the field of polymer science by providing a robust and versatile toolkit for the efficient and selective construction of complex macromolecular architectures. In polymer science, these reac

卵石

顯而易見(jiàn)

,CuAAC ‘Click’ in Carbohydrate Chemistry,and efficient method for the selective modification and conjugation of diverse carbohydrates. This click chemistry reaction enables the formation of stable 1,2,3-triazole linkages, allowing them for the precise attachment of biocompatible carbohydrates to various functional groups, probes, and biomo

PARA

Click Chemistry in Nucleic Acids, a reliable and versatile method for modifying DNA and RNA. This modular reaction facilitates the efficient and selective formation of 1,2,3-triazole linkages between azide and alkyne functional groups, enabling the precise conjugation of nucleic acids with various molecular entities. CuAAC is instr

Incise

Growing Opportunities of Click Chemistry in Drug Development,emistry. This reaction, known for its specificity, efficiency, and biocompatibility, allows for the rapid and reliable formation of 1,2,3-triazoles by joining azides and alkynes. CuAAC’s versatility has been harnessed for various applications, including drug discovery, bioconjugation, and the develo

ANTI

Click-Mediated 1,2,3-Triazoles in Catalysis,espite using triazolyl moiety in metal catalysis, we also highlighted the triazolyl scaffolds as organocatalysts for the stereoselective organic transformation reactions. There are several triazolyl metal-ion ligands utilized in catalysis, but greater research into metal–triazolyl interactions may l

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ERUPT

Tandem/MCR Click Chemistry in Organic Synthesis,ectures from simple building blocks in a single reaction sequence. By integrating multiple click reactions, such as Cu(I)-catalyzed azide-alkyne cycloaddition (CuAAC), Ru-catalyzed azide-alkyne cycloaddition (RuAAC), this approach offers exceptional modularity, selectivity, and functional group comp

強(qiáng)壯

Post-functionalization of Click-Derived 1,2,3-Triazoles,ften selective, chemical reaction. This technique leverages the high efficiency and specificity of click chemistry to initially construct a core structure, which is subsequently adorned with various functional groups. The approach significantly expands the chemical diversity and applicability of the

彎腰

Institut für Afrika-Kunde,Rolf Hofmeierg the labeling and tracking of biomolecules in real time, providing invaluable insights into biological functions that eventually can revolutionized molecular imaging, drug delivery, and therapeutic strategies.