Authors:
Rosse, G
Gerber, F
Specklin, JL
Hubschwerlen, C
Citation: G. Rosse et al., A novel synthesis of beta-sulfinyl- and beta-sulfonyl-hydroxamic acids viaCsF-mediated ring opening of substituted beta-lactones, SYNLETT, (4), 2001, pp. 538-540
Authors:
Apfel, CM
Evers, S
Hubschwerlen, C
Pirson, W
Page, MGP
Keck, W
Citation: Cm. Apfel et al., Peptide deformylase as an antibacterial drug target: Assays for detection of its inhibition in Escherichia coli cell homogenates and intact cells, ANTIM AG CH, 45(4), 2001, pp. 1053-1057
Authors:
Apfel, CM
Locher, H
Evers, S
Takacs, B
Hubschwerlen, C
Pirson, W
Page, MGP
Keck, W
Citation: Cm. Apfel et al., Peptide deformylase as an antibacterial drug target: Target validation andresistance development, ANTIM AG CH, 45(4), 2001, pp. 1058-1064
Citation: P. Hilty et al., Expeditious solution phase synthesis of fluoroquinolone antibacterial agents using polymer supported reagents, TETRAHEDR L, 42(9), 2001, pp. 1645-1646
Authors:
Apfel, C
Banner, DW
Bur, D
Dietz, M
Hubschwerlen, C
Locher, H
Marlin, F
Masciadri, R
Pirson, W
Stalder, H
Citation: C. Apfel et al., 2-(2-oxo-1,4-dihydro-2H-quinazolin-3-yl)- and 2-(2,2-dioxo-1,4-dihydro-2H-2 lambda(6)-benzo[1,2,6]thiadiazin-3-yl)-N-hydroxy-acetamides as potent andselective peptide deformylase inhibitors, J MED CHEM, 44(12), 2001, pp. 1847-1852
Authors:
Apfel, C
Banner, DW
Bur, D
Dietz, M
Hirata, T
Hubschwerlen, C
Locher, H
Page, MGP
Pirson, W
Rosse, G
Specklin, JL
Citation: C. Apfel et al., Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agents, J MED CHEM, 43(12), 2000, pp. 2324-2331