Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
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Synthesis of New Peptidic Glycoclusters Derived from β-Alanine. Part 2: Optionally Modulated Distance between Side-Chain Branched Points
Noriyasu HadaKoji SatoYuhua JinTadahiro Takeda
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2005 Volume 53 Issue 9 Pages 1131-1135

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Abstract
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.
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© 2005 The Pharmaceutical Society of Japan
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