P. Dudfield

发表

The design and synthesis of inhibitors of adenosine 5'-monophosphate deaminase.

C. Earnshaw, J. Dancer, S. Lindell, 1999, Bioorganic & medicinal chemistry letters.

Synthesis of C-ribosyl imidazo[2,1-f][1,2,4]triazines as inhibitors of adenosine and AMP deaminases

S. Lindell, P. Dudfield, C. Rees, 1999 .

Camphorsulfonamide-Shielded, Asymmetric 1,4-Additions and Enolate Alkylations; Synthesis of a Southern Corn Rootworm Pheromone. Preliminary Communication†

W. Oppolzer, P. Dudfield, T. Godel, 1985 .

Synthesis of C-ribosyl 1,2,4-triazolo[3,4-f][1,2,4]triazines as inhibitors of adenosine and AMP deaminases

S. Lindell, P. Dudfield, C. Rees, 1999 .

Asymmetric halogenation of camphor-10-sulfonic acid derived esters: an efficient new route to enantiomerically pure halohydrins and epoxides.

W. Oppolzer, P. Dudfield, 1986 .

Asymmetric α-Acetoxylation of Carboxylic Esters. Preliminary Communication†

W. Oppolzer, P. Dudfield, 1985 .

Synthesis of Quinones

P. Dudfield, 1991 .

(±)‐Carbocyclic (E)‐5‐(2‐bromovinyl)‐2′‐deoxyuridine: A Potent Antiherpes Agent.

P. Ravenscroft, J. Cameron, R. Cookson, 1985 .

Synthesis of carbocyclic C-nucleoside analogues from 8,9,10-trinorborn-5-en-2-ol

R. Cookson, D. Scopes, P. Dudfield, 1986 .

Synthesis of the carbocyclic analogue of the antiviral nucleoside (E)-5-(2-bromovinyl)-2′-deoxyuridine

R. Cookson, D. Scopes, P. Dudfield, 1986 .

A Convenient Synthesis of 2-Cyanoimidazoles

P. Dudfield, K. Hamilton, D. J. Simpson, 1990 .

2.10 – Vinylic and Arylic CH Oxidation

P. Dudfield, 1991 .