Article: Advances on the Synthesis of C-Aryl-glycosides Since 2019
2024
Abstract: Aryl-glycosides represent a significant subclass of crucial glycosidic compounds, increasingly capturing the attention of pharmaceutical developers as bioelectronic motifs embedded within glycosides. Their outstanding resistance to enzymatic hydrolysis ... ...
Abstract | Aryl-glycosides represent a significant subclass of crucial glycosidic compounds, increasingly capturing the attention of pharmaceutical developers as bioelectronic motifs embedded within glycosides. Their outstanding resistance to enzymatic hydrolysis bestows a distinctive advantage in the field of drug development, particularly in therapeutic domains such as diabetes treatment, where pharmaceuticals based on the C -aryl-glycoside architecture manifest compelling therapeutic efficacy. As a result, researchers in the realm of synthetic chemistry have diligently explored and devised a plethora of streamlined and efficacious synthetic methodologies. This comprehensive account systematically delineates methodologies employed in recent years for the efficient synthesis of C -aryl-glycosides, offering insights into three primary directions: transition-metal catalysis, radical strategies, and metal-free catalysis processes. 1 Introduction 2 Glycosylation via Transition-Metal Catalytic Approaches 3 Glycosylation via Glycosyl Radical Approaches 4 Glycosylation via Metal-Free Catalytic Approaches 5 Conclusion and Outlook |
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Keywords | -aryl-glycosides ; glycosylation ; transition-metal catalysis ; glycosyl radical ; metal-free catalysis |
Language | English |
Publishing date | 2024-03-07 |
Publisher | Georg Thieme Verlag KG |
Publishing place | Stuttgart ; New York |
Document type | Article |
ZDB-ID | 2042012-2 |
ISSN | 1437-2096 ; 0936-5214 |
ISSN (online) | 1437-2096 |
ISSN | 0936-5214 |
DOI | 10.1055/a-2283-0623 |
Database | Thieme publisher's database |
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