抄録
The synthesis of an asymmetric glycocluster 1 has been achieved using two glycocluster units 12 and 13, prepared by coupling the cluster chain unit 4 with each ω-amino acid (β-alanine and 6-aminocapronic acid) trichloroethyl ester, and peptidic C-terminal block glycocluster 16, prepared by coupling the bifunctional linker 14 with sugar unit 9. This method facilitated the synthesis of the cluster optionally modulated the distance between the side-chain branched points by using various ω-amino acids. We also synthesized glycodendron 2 using the same intermediate.
本文言語 | English |
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ページ(範囲) | 1131-1135 |
ページ数 | 5 |
ジャーナル | Chemical and Pharmaceutical Bulletin |
巻 | 53 |
号 | 9 |
DOI | |
出版ステータス | Published - 2005 9月 |
外部発表 | はい |
ASJC Scopus subject areas
- 化学 (全般)
- 創薬