Evans GB - Search Results

1

The synthesis and antibacterial activity of totarol derivatives. Part 1: modifications of ring-C and pro-drugs.

Evans GB, Furneaux RH, Gravestock MB, Lynch GP, Scott GK. Evans GB, et al. Bioorg Med Chem. 1999 Sep;7(9):1953-64. doi: 10.1016/s0968-0896(99)00162-5. Bioorg Med Chem. 1999. PMID: 10530944

2

Exploring structure-activity relationships of transition state analogues of human purine nucleoside phosphorylase.

Evans GB, Furneaux RH, Lewandowicz A, Schramm VL, Tyler PC. Evans GB, et al. J Med Chem. 2003 Jul 17;46(15):3412-23. doi: 10.1021/jm030145r. J Med Chem. 2003. PMID: 12852771

3

The synthesis and antibacterial activity of totarol derivatives. Part 2: Modifications at C-12 and O-13.

Evans GB, Furneaux RH. Evans GB, et al. Bioorg Med Chem. 2000 Jul;8(7):1653-62. doi: 10.1016/s0968-0896(00)00095-x. Bioorg Med Chem. 2000. PMID: 10976513

4

The synthesis and antibacterial activity of totarol derivatives. Part 3: Modification of ring-B.

Evans GB, Furneaux RH, Gainsford GJ, Murphy MP. Evans GB, et al. Bioorg Med Chem. 2000 Jul;8(7):1663-75. doi: 10.1016/s0968-0896(00)00096-1. Bioorg Med Chem. 2000. PMID: 10976514

5

8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases.

Evans GB, Furneaux RH, Gainsford GJ, Hanson JC, Kicska GA, Sauve AA, Schramm VL, Tyler PC. Evans GB, et al. J Med Chem. 2003 Jan 2;46(1):155-60. doi: 10.1021/jm0203332. J Med Chem. 2003. PMID: 12502369

6

Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase.

Evans GB, Furneaux RH, Lewandowicz A, Schramm VL, Tyler PC. Evans GB, et al. J Med Chem. 2003 Nov 20;46(24):5271-6. doi: 10.1021/jm030305z. J Med Chem. 2003. PMID: 14613329

7

Imino-C-nucleoside synthesis: heteroaryl lithium carbanion additions to a carbohydrate cyclic imine and nitrone.

Evans GB, Furneaux RH, Hausler H, Larsen JS, Tyler PC. Evans GB, et al. J Org Chem. 2004 Mar 19;69(6):2217-20. doi: 10.1021/jo035744k. J Org Chem. 2004. PMID: 15058979

8

Targeting the polyamine pathway with transition-state analogue inhibitors of 5'-methylthioadenosine phosphorylase.

Evans GB, Furneaux RH, Schramm VL, Singh V, Tyler PC. Evans GB, et al. J Med Chem. 2004 Jun 3;47(12):3275-81. doi: 10.1021/jm0306475. J Med Chem. 2004. PMID: 15163207

9

Second generation transition state analogue inhibitors of human 5'-methylthioadenosine phosphorylase.

Evans GB, Furneaux RH, Lenz DH, Painter GF, Schramm VL, Singh V, Tyler PC. Evans GB, et al. J Med Chem. 2005 Jul 14;48(14):4679-89. doi: 10.1021/jm050269z. J Med Chem. 2005. PMID: 16000004

10

A practical synthesis of (3R,4R)-N-tert-butoxycarbonyl-4-hydroxymethylpyrrolidin-3-ol.

Clinch K, Evans GB, Furneaux RH, Lenz DH, Mason JM, Mee SP, Tyler PC, Wilcox SJ. Clinch K, et al. Among authors: evans gb. Org Biomol Chem. 2007 Sep 7;5(17):2800-2. doi: 10.1039/b708796a. Epub 2007 Jul 20. Org Biomol Chem. 2007. PMID: 17700848

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