Highly Efficient Chemoenzymatic Synthesis of Naturally Occurring and Non-Natural α-2,6-Linked Sialosides: AP. damsela α-2,6-Sialyltransferase with Extremely Flexible Donor–Substrate Specificity
- 1 June 2006
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 118 (24) , 4042-4048
- https://doi.org/10.1002/ange.200600572
Abstract
No abstract availableKeywords
This publication has 56 references indexed in Scilit:
- Evidence of Regio-specific Glycosylation in Human Intestinal MucinsJournal of Biological Chemistry, 2003
- Recent Advances in the Synthesis of Sialic Acid Derivatives and Sialylmimetics as Biological ProbesChemical Reviews, 2002
- Chemical Diversity in the Sialic Acids and Related α-Keto Acids: An Evolutionary PerspectiveChemical Reviews, 2002
- Diversity of sialic acids revealed using gas chromatography/mass spectrometry of heptafluorobutyrate derivativesGlycobiology, 2001
- Microbial Sialyltransferases for Carbohydrate Synthesis.Trends in Glycoscience and Glycotechnology, 2001
- Recent Advances in O-SialylationChemical Reviews, 2000
- Achievements and challenges of sialic acid researchGlycoconjugate Journal, 2000
- Enzyme-Catalyzed Synthesis of Oligosaccharides That Contain Functionalized Sialic AcidsJournal of the American Chemical Society, 1997
- Synthese des Trisaccharids Neu-5-Ac-α(2→6)Gal-β(1→4)GlcNAc mit immobilisierten EnzymenAngewandte Chemie, 1986
- Synthesis of the Trisaccharide Neu‐5‐Ac‐α(2→6)Gal‐β(1→4)GlcNAc by the Use of Immobilized EnzymesAngewandte Chemie International Edition in English, 1986