Rapid assembly of oligosaccharides: 1,2-diacetal-mediated reactivity tuning in the coupling of glycosyl fluorides (Q56953247)

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Luke G Green

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Michael G Hahn

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Berthold Hinzen

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Stuart J Ince

Eukaryotic glycosylation: whim of nature or multipurpose tool?

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publication date

January 2000

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published in

Tetrahedron: Asymmetry

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volume

11

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issue

1

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page(s)

173-197

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cites work

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Selectinminus signCarbohydrate Interactions: From Natural Ligands to Designed Mimics

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7 January 2021

Dispiroketals in synthesis (part 2): A new group for the selective protection of diequatorial vicinal diols in carbohydrates

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Dispiroketals in synthesis (Part 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptors

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Total synthesis of the protein phosphatase inhibitor okadaic acid

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Rapid access to rare natural pyranosides using 1,2-diacetal protected intermediates

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Preparation, structure, derivatisation and NMR data of cyclohexane-1,2-diacetal protected carbohydrates

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Direct preparation of diacetals from 1,2-diketones and their use as 1,2-diol protecting groups

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Cyclohexane-1,2-diacetals(CDA): A New Protecting Group for Vicinal Diols in Carbohydrates

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A New Strategy for Oligosaccharide Assembly Exploiting Cyclohexane-1,2-diacetal Methodology: An Efficient Synthesis of a High Mannose Type Nonasaccharide

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7 January 2021

1,2-Diacetals in Synthesis: Total Synthesis of a Glycosylphosphatidylinositol Anchor ofTrypanosoma brucei

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7 January 2021

A Facile One-Pot Synthesis of a Trisaccharide Unit from the Common Polysaccharide Antigen of Group BStreptococci Using Cyclohexane-1, 2-diacetal(CDA) Protected Rhamnosides

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7 January 2021

Thioglycosides as glycosyl donors in oligosaccharide synthesis.

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One-pot Synthesis of Penta- and Hepta-saccharides from Monomeric Mannose Building Blocks Using the Principles of Orthogonality and Reactivity Tuning

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Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesis

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Glycosylation using a one-electron-transfer, homogeneous reagent. Application to an efficient synthesis of the trimannosyl core of N-glycosylproteins

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The structure, biosynthesis and function of glycosylated phosphatidylinositols in the parasitic protozoa and higher eukaryotes

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Biosynthesis of glycosylphosphatidylinositols in mammals and unicellular microbes.

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Rapid Assembly of Oligosaccharides: Total Synthesis of a Glycosylphosphatidylinositol Anchor of Trypanosoma brucei

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Stereoselective synthesis of glycobiosyl phosphatidylinositol, a part structure of the glycosyl-phosphatidylinositol (GPI) anchor of Trypanosoma brucei

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Stereoselective total synthesis of the glycosyl phosphatidylinositol (GPI) anchor of Trypanosoma brucei

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Glycosyl Inositol Derivatives Related to Inositolphosphoglycan Mediators: Synthesis, Structure, and Biological Activity

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Structure-activity relationship of synthetic phosphoinositolglycans mimicking metabolic insulin action

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Parasite glycoconjugates. Part 7.1 Synthesis of further substrate analogues of early intermediates in the biosynthetic pathway of glycosylphosphatidylinositol membrane anchors

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Synthesis of a partially protected 1d-6-O-(2-azido-2-deoxy-α-d-glucopyranosyl)-myo-inositol: a useful precursor of glycosylphosphatidylinositols and related compounds

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Alternative lipid remodelling pathways for glycosylphosphatidylinositol membrane anchors in Saccharomyces cerevisiae

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Iodine: A versatile reagent in carbohydrate chemistry IV. Per-O-acetylation, regioselective acylation and acetolysis

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7 January 2021