Moenomycin analogues with long-chain amine lipid parts from reductive aminations

19Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free