Literature DB >> 35513346

HPLC-Based Automated Synthesis of Glycans in Solution.

Samira Escopy1,2, Yashapal Singh1, Keith J Stine1, Alexei V Demchenko1,2.   

Abstract

As the 21st century unfolds with rapid changes, new challenges in research and development emerge. These new challenges prompted us to repurpose our HPLC-A platform that was previously used in solid phase glycan synthesis to a solution phase batch synthesis described herein. The modular character of HPLC allows for implementing new attachments. To enable sequential synthesis of multiple oligosaccharides with the single press of a button, we supplemented our system with a four-way split valve and an automated fraction collector. This enabled the operator to load all reagents and all reactants in the autosampler, press the button to start the repetitive automation sequence, leave the lab, and upon return find products of multiple reactions ready for purification, analysis, and subsequent application.
© 2022 Wiley-VCH GmbH.

Entities:  

Keywords:  automation; glycans; glycosylation; oligosaccharides; synthesis

Mesh:

Substances:

Year:  2022        PMID: 35513346      PMCID: PMC9403992          DOI: 10.1002/chem.202201180

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.020


  65 in total

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Journal:  J Org Chem       Date:  2019-05-17       Impact factor: 4.354

5.  Challenges in the Conversion of Manual Processes to Machine-Assisted Syntheses: Activation of Thioglycoside Donors with Aryl(trifluoroethyl)iodonium Triflimide.

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Journal:  Org Lett       Date:  2018-01-16       Impact factor: 6.005

6.  The chemical synthesis of human milk oligosaccharides: Lacto-N-tetraose (Galβ1→3GlcNAcβ1→3Galβ1→4Glc).

Authors:  Mithila D Bandara; Keith J Stine; Alexei V Demchenko
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10.  Automated Solution-Phase Synthesis of Insect Glycans to Probe the Binding Affinity of Pea Enation Mosaic Virus.

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Journal:  J Org Chem       Date:  2015-10-12       Impact factor: 4.354

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  1 in total

1.  Recyclable fluorous-tag assisted two-directional oligosaccharide synthesis enabled by interrupted Pummerer reaction mediated glycosylation.

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  1 in total

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