Efficient Synthesis of the Disialylated Tetrasaccharide Motif in N-Glycans through an Amide-Protection Strategy-Reference-Cited by-同舟云学术

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Efficient Synthesis of the Disialylated Tetrasaccharide Motif in N-Glycans through an Amide-Protection Strategy

Published:2016-04-08 Issue:9 Volume:11 Page:1436-1440
ISSN:1861-4728
Container-title:Chemistry - An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Zhou Jiazhou¹,Manabe Yoshiyuki¹,Tanaka Katsunori²,Fukase Koichi¹

Affiliation:

1. Department of Chemistry, Graduate School of Science; Osaka University; Machikaneyama 1-1 Toyonaka Osaka 560-0043 Japan

2. Biofunctional Synthetic Chemistry Laboratory; RIKEN; Hirosawa 2-1 Wako Saitama 351-0198 Japan

Funder

Grant-in-Aid for Scientific Research on Innovative Areas: Middle Molecular Strategy

MEXT

Grant-in-Aid for Scientific Research on Innovative Areas: Integrated Organic Synthesis

Grant-in-Aid for Scientific Research

JSPS

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/asia.201600139/fullpdf

Reference29 articles.

1. Enhancement of therapeutic protein in vivo activities through glycoengineering

2. Glycoinsulins: Dendritic Sialyloligosaccharide-Displaying Insulins Showing a Prolonged Blood-Sugar-Lowering Activity

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3. Synthetic Study of Bio-functional Glycans;Modern Natural Product Synthesis;2024

4. Diacetyl strategy for synthesis of NHAc containing glycans: enhancing glycosylation reactivity via diacetyl imide protection;Frontiers in Chemistry;2023-12-05

5. Chemical Biology Study for Elucidating and Regulating Emergent Glycan Functions;Journal of Synthetic Organic Chemistry, Japan;2023-02-01

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