An alternative high yielding and highly stereoselective method for preparing an α-Neu5NAc-(2,6)-d-GalN3 building block suitable for further glycosylation-Reference-Cited by-同舟云学术

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An alternative high yielding and highly stereoselective method for preparing an α-Neu5NAc-(2,6)-d-GalN3 building block suitable for further glycosylation

Published:2005-08 Issue:11 Volume:340 Page:1885-1892
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Laurent Nicolas,Lafont Dominique,Boullanger Paul,Mallet Jean Maurice

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference30 articles.

1. Structure, function and metabolism of sialic acids

2. Glyco-Sciences, Status and Perspectives;Reutter,1997

3. Recent Advances in O-Sialylation

4. RECENT DEVELOPMENTS IN TECHNOLOGY FOR GLYCOSYLATION WITH SIALIC ACID

5. Glycolipid and Monoclonal Immunoglobulin−Glycolipidic Liposomes Spread onto High Ionic Strength Buffers: Evidence for a True Monolayer Formation

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1. Cu(I)-Catalyzed Click Chemistry in Glycoscience and Their Diverse Applications;Chemical Reviews;2021-06-24

2. Acyl Migrations in Carbohydrate Chemistry;Protecting Groups;2018-11-19

3. Protecting Groups at the Secondary Positions of Carbohydrates;Protecting Groups;2018-11-19

4. N ‐protecting Groups for 2‐Amino‐2‐deoxy‐glycosides;Protecting Groups;2018-11-19

5. Cu-Catalyzed Click Reaction in Carbohydrate Chemistry;Chemical Reviews;2016-01-22

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