Ft. Ferse et al., Acceptor site recognition of transglycosylase inhibitors - A beta-D-glucopyranosyl-(1 -> 2)-alpha-D-glucopyranuronamide-derived moenomycin analogue, TETRAHEDRON, 55(12), 1999, pp. 3749-3766
The synthesis, the antibiotic and the transglycosylase inibiting properties
of a disaccharide analogue of moenomycin A in which the NHAc group of unit
E is replaced by a hydroxyl function are described. It can be concluded th
at this NHAc group is essential for eliciting transglycosylase inhibiting p
roperties, in agreement with a recently established solution structure of m
oenomycin A. (C) 1999 Elsevier Science Ltd. All rights reserved.