The synthesis of 5-amino-5-deoxy-1,2-O-(S)-trichloroethylidene-beta-L-arabinofuranose and 6-amino-6-deoxy-1,2-O-(S)-trichloroethylidene-alpha-D-glucofuranose is described by a simple three- or four-step route. Antibacterial potency of the new compounds was determined using an inhibition zone diameter test. The results show that these compounds have a broad-spectrum activity against Gram-positive, Gram-negative bacteria and Candida albicans.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.carres.2010.03.043 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!