Tetrahedron p. 1695 - 1706 (1997)
Update date:2022-08-04
Topics:
Range, Gerhard
Kraehmer, Ralf
Welzel, Peter
Mueller, Dietrich
Herrmann, Guido F.
Kragl, Udo
Wandrey, Christian
Markus, Astrid
Van Heijenoort, Yveline
Van Heijenoort, Jean
The trisaccharide moenomycin analogue 1c has been synthesized. One starting material was N-acetyllactosamine obtained by an enzyme-catalyzed transglycosylation. 1c differs from moenomycin degradation product 1a only in two positions of unit C. In contrast to 1a the synthetic 1c is antibiotically inactive.
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