Convenient Synthesis and Purification ofN-Trifluoroacetylated Neuraminic Acid Tetraol: A Key Precursor for the Synthesis of New Sialyl Donors Containing LabileO-Acyl Protecting Groups
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference39 articles.
1. Biochemistry of Sialic Acid Diversity
2. Chemical Diversity in the Sialic Acids and Related α-Keto Acids: An Evolutionary Perspective
3. Glycan-based interactions involving vertebrate sialic-acid-recognizing proteins
4. Selective α-Sialylation
5. Recent Strategies for Stereoselective Sialylation and Their Application to the Synthesis of Oligosialosides
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1. Synthesis of sialyl halides with various acyl protective groups;Carbohydrate Research;2024-02
2. Azidation of Partially Protected Carbohydrate Derivatives: Efficient Suppression of Acyl Migration;Synlett;2020-06-09
3. Chemical Synthesis of Glycosides of N-Acetylneuraminic Acid;Advances in Carbohydrate Chemistry and Biochemistry;2018
4. Stereoselective sialylation with O-trifluoroacetylated thiosialosides: hydrogen bonding involved?;Carbohydrate Research;2017-11
5. Electrospray ionization mass spectra of derivatives of 2-phenylthio-N-trifluoroacetylneuraminic acid;Journal of Analytical Chemistry;2015-12
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