51450-25-0Relevant articles and documents
A chemoenzymatic approach towards moenomycin structural analogues
Range, Gerhard,Kraehmer, Ralf,Welzel, Peter,Mueller, Dietrich,Herrmann, Guido F.,Kragl, Udo,Wandrey, Christian,Markus, Astrid,Van Heijenoort, Yveline,Van Heijenoort, Jean
, p. 1695 - 1706 (1997)
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.