Efficient synthesis of α-galactosylceramide and its C-6 modified analogs
The synthesis of α-galactosylceramide (KRN7000) and its C-6 modified analogs remains a challenge due to the difficult α-1,2-cis-glycosidic bond. A non-participating benzyl (Bn) protecting group has been commonly used to favor the α-glycosylation product. Here, we report the α-selective glycosylation...
Main Authors: | Huiting Li, Hongzhao Mao, Chao Chen, Ying Xu, Shuai Meng, Tiantian Sun, Chengli Zong |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-11-01
|
Series: | Frontiers in Chemistry |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fchem.2022.1039731/full |
Similar Items
-
Characterization of a Glycolipid Synthase Producing α-Galactosylceramide in <i>Bacteroides fragilis</i>
by: Marc Caballé, et al.
Published: (2022-11-01) -
Depletion of Thymus-Derived CD4+CD25+ T Cells Abrogates the Suppressive Effects of α-galactosylceramide Treatment on Experimental Allergic Conjunctivitis
by: Atsuki Fukushima, et al.
Published: (2008-01-01) -
Evaluating α-galactosylceramide as an adjuvant for live attenuated influenza vaccines in pigs
by: Bianca L. Artiaga, et al.
Published: (2022-08-01) -
Comparison of oseltamivir and α-galactosylceramide for reducing disease and transmission in pigs infected with 2009 H1N1 pandemic influenza virus
by: Darling Melany de C. Madrid, et al.
Published: (2022-10-01) -
Activation of Invariant Natural Killer T Cell Subsets in C57BL/6J Mice by Different Injection Modes of α-galactosylceramide
by: Ming Meng, et al.
Published: (2020-02-01)