Titlebook: Chemistry of 1,2,3-triazoles; Wim Dehaen,Vasiliy A. Bakulev Book 2015 Springer International Publishing Switzerland 2015 carbohydrate chem

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Synthesis of 2,-1,2,3-Triazoles,ns. Moreover, it will give some insights on the reaction mechanisms and will explain how different conditions and structure substrates can influence the direction for reactions. An extensive analysis for the last 20 years (starting at 1990) of NH-1,2,3-triazoles chemistry is presented. Some older da

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Biological Properties of 1,-1,2,3- and 2,-1,2,3-Triazoles, because of their broad range of biological activities. More recently, there has been significant interest in the development of novel triazoles with anti-inflammatory, antiplatelet, antimicrobial, antimycobacterial, antitumoral, and antiviral properties and activity against several neglected diseas

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Mesoionic 1,2,3-Triazoles and 1,2,3-Triazole Carbenes,-triazolylidenes as ligands for transition metals. The organometallic complexes containing this kind of .-heterocyclic carbene ligands (NHCs) have shown to possess unique structural characteristics, including a relatively high covalent contribution to the metal–NHC bond, a strong donor ability, and

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1,2,3-Triazoles Fused to Aromatic Rings,n two groups by a structural approach: (a) fused 1,2,3-triazoles without a bridgehead nitrogen atom and (b) fused 1,2,3-triazoles with a bridgehead nitrogen atom. Although both systems present a similar structure, the synthetic procedures and their reactivity are different.

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Book 2015the scope is to cover topics dealing with all areas within heterocyclic chemistry, both experimental and theoretical, of interest to the general heterocyclic chemistry community. The series consists of topic related volumes edited by renowned editors with contributions of experts in the field.

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