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- W2950663668 endingPage "1252" @default.
- W2950663668 startingPage "1243" @default.
- W2950663668 abstract "Abstract The imposing structural complexity and heterogeneity of glycans has made the study of their precise biological roles challenging. However, recently developed synthetic and screening techniques have enabled the study of many aspects of glycan activity that were previously inaccessible. Among these new methods, the Copper(I)‐catalyzed Azide–Alkyne [3+2] Cycloaddition (CuAAC) has provided a means to mimic multivalent glycan display, manipulate cellular glycans in vivo for visualization and isolation, and generate useful inhibitors of glycoprotein processing." @default.
- W2950663668 created "2019-06-27" @default.
- W2950663668 creator A5010126501 @default.
- W2950663668 creator A5030444638 @default.
- W2950663668 creator A5056753239 @default.
- W2950663668 date "2007-12-01" @default.
- W2950663668 modified "2023-10-17" @default.
- W2950663668 title "Probing Glycans With the Copper(I)‐Catalyzed [3+2] Azide–Alkyne Cycloaddition" @default.
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