Authors: Nicolaou, KC Cho, SY Hughes, R Winssinger, N Smethurst, C Labischinski, H Endermann, R

Citation: Kc. Nicolaou et al., Solid- and solution-phase synthesis of vancomycin and vancomycin analogueswith activity against vancomycin-resistant bacteria, CHEM-EUR J, 7(17), 2001, pp. 3798-3823

Authors: Nicolaou, KC Hughes, R Cho, SY Winssinger, N Labischinski, H Endermann, R

Citation: Kc. Nicolaou et al., Synthesis and biological evaluation of vancomycin dimers with potent activity against vancomycin-resistant bacteria: target-accelerated combinatorialsynthesis, CHEM-EUR J, 7(17), 2001, pp. 3824-3843

Authors: Rudolph, J Theis, H Hanke, R Endermann, R Johannsen, L Geschke, FU

Citation: J. Rudolph et al., seco-cyclothialidines: New concise synthesis, inhibitory activity toward bacterial and human DNA topoisomerases, and antibacterial properties, J MED CHEM, 44(4), 2001, pp. 619-626

Authors: Nicolaou, KC Hughes, R Cho, SY Winssinger, N Smethurst, C Labischinski, H Endermann, R

Citation: Kc. Nicolaou et al., Target-accelerated combinatorial synthesis and discovery of highly potent antibiotics effective against vancomycin-resistant bacteria, ANGEW CHEM, 39(21), 2000, pp. 3823

Authors: Matassova, NB Rodnina, MV Endermann, R Kroll, HP Pleiss, U Wild, H Wintermeyer, W

Citation: Nb. Matassova et al., Ribosomal RNA is the target for oxazolidinones, a novel class of translational inhibitors, RNA, 5(7), 1999, pp. 939-946

Authors: Riedl, B Endermann, R

Citation: B. Riedl et R. Endermann, Recent developments with oxazolidinone antibiotics, EXPERT OP T, 9(5), 1999, pp. 625-633