Stereoselective synthesis of a C -glycoside analogue of N -Fmoc-serine β- N -acetylglucosaminide by ramberg–bäcklund rearrangement-Reference-Cited by-同舟云学术

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Stereoselective synthesis of a C -glycoside analogue of N -Fmoc-serine β- N -acetylglucosaminide by ramberg–bäcklund rearrangement

Published:2002-04 Issue:7 Volume:12 Page:997-999
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Ohnishi Yuki,Ichikawa Yoshitaka

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference15 articles.

1. Glycosylation of Nucleocytoplasmic Proteins: Signal Transduction and O-GlcNAc

2. Facile synthesis of N-Fmoc-serine-S-GlcNAc: a potential molecular probe for the functional study of O-GlcNAc

3. Methods for Anomeric Carbon-Linked and Fused Sugar Amino Acid Synthesis: The Gateway to Artificial Glycopeptides

4. Asymmetric Strecker Synthesis of C-Glycopeptide

5. N-Halocarbamate Salts Lead to More Efficient Catalytic Asymmetric Aminohydroxylation

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1. The Ramberg–Bäcklund Rearrangement and the Eschenmoser Coupling Reaction;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2024

2. C-Glycosides;Synthesis and Characterization of Glycosides;2022

3. Nucleoside Mimetics;Synthesis and Characterization of Glycosides;2022

4. Glycosides, Synthesis and Characterization;Synthesis and Characterization of Glycosides;2022

5. Synthesis of Symmetrical Dodeco‐6,7‐diuloses;European Journal of Organic Chemistry;2020-06-15

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