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Improved In-gel Reductive β-Elimination for Comprehensive O-linked and Sulfo-glycomics by Mass Spectrometry
Published on: November 20, 2014
Synthesis and conformational analysis of neoglycoconjugates derived from O- and S-glucose
Víctor Rojas1, Javier Carreras, Francisco Corzana
1Departamento de Química, Universidad de La Rioja, Centro de Investigación en Síntesis Química, Logroño, La Rioja, Spain.
Abstract:
Using olefin metathesis as a key step, four neoglycoconjugates incorporating α-O-glucose, α-S-glucose or β-S-glucose as a carbohydrate unit and L-serine or L-cysteine as an amino acid moiety have been synthesized. The four-atom carbon spacer allows the carbohydrate to explore a wide-ranging conformational space, which may have important implications for the molecular recognition of these molecules.
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