From a moenomycin A glycolic aldehyde degradation product lacking the chromophore unit and most of the lipid part, a number of amines were prepared by reductive amination. Their interaction with artificial membranes as well as their transglycosylase inhibiting and antibiotic properties were studied. © 2001 Elsevier Science Ltd.
Vogel, S., Stembera, K., Hennig, L., Findeisen, M., Giesa, S., Welzel, P., … Lampilas, M. (2001). Moenomycin analogues with long-chain amine lipid parts from reductive aminations. Tetrahedron, 57(19), 4147–4160. https://doi.org/10.1016/S0040-4020(01)00306-4