Authors:
Murray, PJ
Kranz, M
Ladlow, M
Taylor, S
Berst, F
Holmes, AB
Keavey, KN
Jaxa-Chamiec, A
Seale, PW
Stead, P
Upton, RJ
Croft, SL
Clegg, W
Elsegood, MRJ
Citation: Pj. Murray et al., The synthesis of cyclic tetrapeptoid analogues of the antiprotozoal natural product apicidin, BIOORG MED, 11(6), 2001, pp. 773-776
Citation: Ps. Jones et al., Synthesis of tetrasubstituted bicyclo[3.2.1]octenes as potential inhibitors of influenza virus sialidase, BIOORG MED, 9(4), 1999, pp. 605-610
Authors:
Macdonald, SJF
Mills, K
Spooner, JE
Upton, RJ
Dowle, MD
McDonald, E
Citation: Sjf. Macdonald et al., A stereoselective synthesis via a 5-exo-trig cyclisation of trans-2-oxohexahydro-2H-furo[3,2-b]pyrroles (pyrrolidine-trans-lactones) - potent, novel elastase inhibitors (vol 1, pg 3931, 1998), J CHEM S P1, (7), 1999, pp. 833-833
Authors:
MacDonald, SJF
Clarke, GDE
Dowle, MD
Harrison, LA
Hodgson, ST
Inglis, GGA
Johnson, MR
Shah, P
Upton, RJ
Walls, SB
Citation: Sjf. Macdonald et al., A flexible, practical, and stereoselective synthesis of enantiomerically pure trans-5-oxohexahydropyrrolo[3,2-b]pyrroles (pyrrolidine-trans-lactams),a new class of serine protease inhibitors, using acyliminium methodology, J ORG CHEM, 64(14), 1999, pp. 5166-5175
Authors:
Macdonald, SJF
Mills, K
Spooner, JE
Upton, RJ
Dowle, MD
Citation: Sjf. Macdonald et al., A stereoselective synthesis via a 5-exo-trig cyclisation of trans-2-oxohexahydro-2H-furo[3,2-b]pyrroles (pyrrolidine-trans-lactones) - potent, novel elastase inhibitors, J CHEM S P1, (23), 1998, pp. 3931-3936