P. Edwards

发表

Synthesis of derivatives of muramic acid and C-1 homologated α-D-glucose as potential inhibitors of bacterial transglycosylase

R. Southgate, T. C. Smale, G. Brooks, 1995 .

Penem inhibitors of bacterial signal peptidase

R. Southgate, A. Kaura, T. C. Smale, 1995 .

Reactions of 2,2,2-trichloroethyl 6-diazopenicillanate with aromatic aldehydes. X-Ray crystal structures of (3S,8aS)-2,2,2-trichloroethyl 2,3-dihydro-6-(4-methoxyphenyl)-2,2-dimethyl-5-oxo-5H,8aH-thiazolo[2,3-b][1,3]oxazine-3-carboxylate and (2S,5S)-2,2,2-trichloroethyl-4-formyl-2-(4-methoxyphenyl)-

David J. Williams, A. Slawin, P. Edwards, 1986 .

Inhibitors of bacterial signal peptidase: a series of 6-(substituted oxyethyl)penems.

R. Southgate, A. Kaura, A. Allsop, 1996, The Journal of antibiotics.

6-(SUBSTITUTED METHYLENE)PENEMS, POTENT BROAD SPECTRUM INHIBITORS OF BACTERIAL β-LACTAMASE

N. F. Osborne, B. Clarke, K. Coleman, 1991 .

Application of the Suzuki biphenyl synthesis to the natural products biphenomycin and vancomycin

P. Edwards, Allan G. Brown, M. Crimmin, 1992 .

Synthesis of analogues of the biphenomycin antibiotics

P. Edwards, Allan G. Brown, A. G. Brown, 1990 .

Synthesis of an unnatural product -- 4,4' biaryl formation as a macrocyclisation step

G. Langley, J. Kilburn, P. Edwards, 1994 .

Modified synthesis and binding properties of a peptide receptor

J. Dowden, J. Kilburn, P. Edwards, 1997 .

6-(substituted methylene)penems, potent broad spectrum inhibitors of bacterial beta-lactamase. IV. Kidney stability, serum binding and additional biological evaluation of racemic derivatives.

N. F. Osborne, K. Coleman, P. Edwards, 1991, The Journal of antibiotics.