P. Kane

发表

The diazo route to diazonamide A. Studies on the indole bis-oxazole fragment.

C. Moody, J. R. Davies, P. Kane, 2005, The Journal of organic chemistry.

A linker for amidines in solid phase synthesis

M. Bradley, P. Roussel, I. Matthews, 1997 .

Inhibition of the tissue factor/factor VIIa complex — Lead optimisation using combinatorial chemistry

M. Bradley, P. Roussel, A. Cross, 1999 .

The Bohlmann–Rahtz route to functionalised pyridine scaffolds and their use in library synthesis

K. E. Bashford, A. Robertson, M. Warne, 2003 .

N–H Insertion reactions of rhodium carbenoids. Part 5: A convenient route to 1,3-azoles☆

C. Moody, P. Kane, James R. Davies, 2004 .

The preparation and utility of ethyl 2-(5′-O-t-butyldimethylsilyl-2′,3′-O-isopropylidene-β-D-ribofuranosyl)propenoate as a key intermediate for C-nucleoside synthesis

J. Mann, P. Kane, 1984 .

Control of competing N-H insertion and Wolff rearrangement in dirhodium(II)-catalyzed reactions of 3-indolyl diazoketoesters. synthesis of a potential precursor to the marine 5-(3-indolyl)oxazole martefragin A.

A. Slawin, C. Moody, P. Kane, 2005, The Journal of organic chemistry.

The design and synthesis of thrombin inhibitors: analogues of MD805 containing non-polar surrogates for arginine at the P1 position.

D. Brundish, D. Janus, X. Cockcroft, 2000, Bioorganic & medicinal chemistry letters.

N–H Insertion reactions of rhodium carbenoids. Part 3. The development of a modified Bischler indole synthesis and a new protecting-group strategy for indoles

K. E. Bashford, C. Moody, E. Swann, 2002 .

A new protecting-group strategy for indoles

K. E. Bashford, C. Moody, P. Kane, 2002 .

A novel approach to bis-isoxazolines using a latent form of cyclopentadienone

M. Drew, J. Mann, P. Kane, 2000 .

Amidine protection for solution phase library synthesis

P. Kane, Emma L. Baker, C. Bailey, 1999 .

Design and synthesis of thrombin inhibitors: analogues of MD-805 with reduced stereogenicity and improved potency.

M. McDonnell, R. Wakeford, D. Brundish, 1999, Journal of Medicinal Chemistry.

The design and synthesis of thrombin inhibitors: the introduction of in vivo efficacy and oral bioavailability into benzthiazolylalanine inhibitors.

K. Menear, X. Cockcroft, M. Tweed, 2000, Bioorganic & medicinal chemistry letters.

THE PREPARATION AND UTILITY OF ETHYL 2-(5′-O-TERT-BUTYLDIMETHYLSILYL-2′,3′-O-ISOPROPYLIDENE-β-D-RIBOFURANOSYL)P# ROPENOATE AS A KEY INTERMEDIATE FOR C-NUCLEOSIDE SYNTHESIS

J. Mann, P. Kane, 1984 .

Tritium labelling by selective debromination

D. Brundish, P. Kane, 1988 .

The synthesis of [3H]cadralazine of high specific activity

D. Brundish, P. Kane, 1988 .

N—H Insertion Reactions of Rhodium Carbenoids. Part 3. The Development of a Modified Bischler Indole Synthesis and a New Protecting Group Strategy for Indoles.

K. E. Bashford, C. Moody, E. Swann, 2002 .

Optimisation of the P2 pharmacophore in a series of thrombin inhibitors: ion-dipole interactions with lysine 60G.

M. Grütter, J. Priestle, B. Wathey, 1999, Bioorganic & Medicinal Chemistry Letters.