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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...
Autores principales: | Li, Huiting, Mao, Hongzhao, Chen, Chao, Xu, Ying, Meng, Shuai, Sun, Tiantian, Zong, Chengli |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732566/ https://www.ncbi.nlm.nih.gov/pubmed/36505742 http://dx.doi.org/10.3389/fchem.2022.1039731 |
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