Gary B. Evans
Carbohydrate Chemistry Team
Industrial Research Limited
PO Box 31310
Lower Hutt
New Zealand
Name/email consistency: high
- Azetidine based transition state analogue inhibitors of N-ribosyl hydrolases and phosphorylases. Evans, G.B., Furneaux, R.H., Greatrex, B., Murkin, A.S., Schramm, V.L., Tyler, P.C. J. Med. Chem. (2008)
- Second generation transition state analogue inhibitors of human 5'-methylthioadenosine phosphorylase. Evans, G.B., Furneaux, R.H., Lenz, D.H., Painter, G.F., Schramm, V.L., Singh, V., Tyler, P.C. J. Med. Chem. (2005)
- 8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases. Evans, G.B., Furneaux, R.H., Gainsford, G.J., Hanson, J.C., Kicska, G.A., Sauve, A.A., Schramm, V.L., Tyler, P.C. J. Med. Chem. (2003)
- Synthesis of a transition state analogue inhibitor of purine nucleoside phosphorylase via the Mannich reaction. Evans, G.B., Furneaux, R.H., Tyler, P.C., Schramm, V.L. Org. Lett. (2003)
- Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase. Evans, G.B., Furneaux, R.H., Lewandowicz, A., Schramm, V.L., Tyler, P.C. J. Med. Chem. (2003)
- The synthesis and antibacterial activity of totarol derivatives. Part 2: Modifications at C-12 and O-13. Evans, G.B., Furneaux, R.H. Bioorg. Med. Chem. (2000)
- The synthesis and antibacterial activity of totarol derivatives. Part 3: Modification of ring-B. Evans, G.B., Furneaux, R.H., Gainsford, G.J., Murphy, M.P. Bioorg. Med. Chem. (2000)
- The synthesis and antibacterial activity of totarol derivatives. Part 1: modifications of ring-C and pro-drugs. Evans, G.B., Furneaux, R.H., Gravestock, M.B., Lynch, G.P., Scott, G.K. Bioorg. Med. Chem. (1999)
