抄録
An α-selective galactosylation was demonstrated under various conditions. Among these α-galactoside approaches, high α-selectivity was achieved by the virtue of 4,6-O-di-tert-butylsilylene (DTBS) group. Yield was further improved by the influence of a 2-O-benzylated donor compared to 2-O-benzoylated donor. This method was then applied to the first highly stereoselective synthesis of a newly found trisaccharide glycosphingolipid in Zygomycetes species.
本文言語 | English |
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ページ(範囲) | 6647-6650 |
ページ数 | 4 |
ジャーナル | Tetrahedron Letters |
巻 | 47 |
号 | 37 |
DOI | |
出版ステータス | Published - 2006 9 11 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry