Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part
Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase in...
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Veröffentlicht in: | Helvetica chimica acta 2004-07, Vol.87 (7), p.1807-1824 |
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container_title | Helvetica chimica acta |
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creator | Yang, Guangbin Mansourova, Madina Hennig, Lothar Findeisen, Matthias Oehme, Ramona Giesa, Sabine Welzel, Peter |
description | Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase inhibitors in detail and for preparing analogues with improved pharmacokinetic properties. |
doi_str_mv | 10.1002/hlca.200490161 |
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title | Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part |
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