Selective synthesis of α- and β-glycosides of N-acetyl galactosamine using rare earth metal triflates

被引:3
作者
Wang, Jiajia [1 ]
Zhang, Wei [2 ]
Cao, Wei [1 ]
Liu, Kang [1 ]
Su, Shihao [2 ]
Ma, Jing [2 ]
Li, Xia [1 ]
机构
[1] Henan Univ, Affiliated Hosp 1, Joint Natl Lab Antibody Drug Engn, Kaifeng, Henan, Peoples R China
[2] Henan Univ, Inst Chem Biol, Acad Adv Interdisciplinary Studies, Sch Pharm, Kaifeng, Henan, Peoples R China
来源
FRONTIERS IN CHEMISTRY | 2022年 / 10卷
基金
中国国家自然科学基金;
关键词
glycosylation; GalNAc; asialoglycoprotein receptor (ASGPR); hydrogen sulfide; selective; GLYCOSYLATION; NAPHTHALIMIDE; GALECTIN; AFFINITY; PROBE;
D O I
10.3389/fchem.2022.1029911
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Structures containing galactose and GalNAc residues are specifically recognized by asialoglycoprotein receptors, allowing them to selectively internalize by hepatocytes for drug-targeting delivery. However, methods for direct synthesis of GalNAc glycosides are still challenging due to the poor participating group of 2-acetamido. Here, we develop a facile strategy to synthesize various GalNAc glycosides by employing a series of rare earth metal triflates, and the results demonstrate that both alpha-glycosides and beta-glycosides of GalNAc can be obtained by conducting with Hf(OTf)(4) and Sc(OTf)(3), respectively. These applicable results indicate that any interested GalNAc-containing substrates could be prepared by this simple strategy.
引用
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页数:10
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