| Literature DB >> 15542084 |
Takeshi Yamamura1, Noriyasu Hada, Asuka Kaburaki, Kimiaki Yamano, Tadahiro Takeda.
Abstract
Efficient and systematic syntheses of four neutral glycosphingolipids that have been isolated from the metacestodes of Echinococcus multilocularis have been achieved. A key step is the direct glycosylation of galactosyl donors using thioglycosides with benzoyl ceramide in the presence of N-iodosuccinimide (NIS)/TfOH, which gave the desired oligosaccharide derivatives. The fully protected glycosides 13, 20, 22 and 25 were deprotected to give four target glycosphingolipids (1-4).Entities:
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Year: 2004 PMID: 15542084 DOI: 10.1016/j.carres.2004.09.015
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104