A. Crame

Design and synthesis of pyrrolidine-5,5-trans-lactams (5-oxo-hexahydro-pyrrolo[3,2-b]pyrroles) as novel mechanism-based inhibitors of human cytomegalovirus protease. 1. The alpha-methyl-trans-lactam template.

G. Hart, T. Haley, A. Pennell, 2000, Journal of medicinal chemistry.

Design and synthesis of pyrrolidine-5,5-trans-lactams (5-oxohexahydropyrrolo[3,2-b]pyrroles) as novel mechanism-based inhibitors of human cytomegalovirus protease. 2. Potency and chirality.

Peter Ertl, James M. Woolven, P. Ertl, 2002, Journal of medicinal chemistry.

An efficient synthesis of a chiral carbocyclic 2′-deoxyribonucleoside synthon by directed reduction

A. D. Borthwick, A. M. Exall, G. Weingarten, 1994 .

A short, convergent synthesis of two chiral antiviral agents, (+) carbocyclic 2′-deoxy-5-[(E)-2-bromovinyl] uridine and (+) carbocyclic 2′-deoxyGuanosine

A. D. Borthwick, A. M. Exall, G. Weingarten, 1995 .

An improved synthesis of the strained pyrrolidine-5,5-translactam ring system

A. Pennell, A. Mason, A. D. Borthwick, 1999 .

A Short, Convergent Synthesis of Two Chiral Antiviral Agents, (+)- Carbocyclic 2′-Deoxy-5-((E)-2-Bromovinyl) Uridine and (+)-Carbocyclic 2′-Deoxyguanosine.

A. D. Borthwick, A. M. Exall, G. Weingarten, 1996 .

Synthesis of Benzodioxinopyrroles as selective α2-adrenoceptor antagonists

P. Procopiou, P. C. Cherry, A. Pipe, 1995 .