Griffith University

Refereed journal articles

1. Camp, D.; Avery, V.; Street, I.; Quinn, R. J. Progress towards establishing an open access molecular screening capability in the Australasian region. ACS Chem. Biol. 2007, 2, accepted for publication.
2. Camp, D. Establishment of an open access compound management facility in Australia to stimulate applied, basic and translational biomedical research. Drug Discovery World 2007, 61.
3. Camp, D.; Quinn, R. J. Biodiscovery for natural product pharmaceuticals: an Australian experience. J. Biolaw and Bus., Special Supplement: Australia 2007, 39.
4. Camp, D.; Quinn, R. J. The evolution of compound libraries for applied and basic research. Chemistry in Australia 2007, 74, 14.
5. Camp, D.; Carroll, A.; Avery, V.; Walve, P.; Jenkins, I. D.; Quinn, R. J. Screening nature: natural products challenge scientific rules and increase screening hit rates. PharmaTechnology 2006, 36.
6. Camp, D.; Li, Y.; McCluskey, A.; Moni, R. W.; Quinn, R. J. Diimidazo [1,2-c:4',5'-e]pyrimidines: N⁶-N¹ conformationally restricted adenosines. Bioorg. Med. Chem. Lett. 1998, 8, 695.
7. Camp, D.; Green, J. M.; Kaiser, S. M.; Moni, R. W.; Townsend-Nicholson, A.; Schofield, P. R.; Quinn, R. J. Diimidazo [1,2-c:4',5'-e]pyrimidines: adenosines agonist activity demonstrated by microphysiometry. Bioorg. Med. Chem. Lett. 1998, 8, 691.
8. Mander, L. N.; Sherburn, M.; Camp, D.; King, R. W.; Evans, L. T.; Pharris, R. P. Effects of D-ring modified gibberellins on flowering and growth in Lolium Temulentum. Phytochemistry 1998, 49, 2195.
9. Mander, L. N.; Adamson, G.; Bhaskar, V. K.; Twitchin, B.; Camp, D.; King, R. W.; Evans, L. T. Effects of 17-Alkyl-16,17-dihydrogibberellin A5 derivatives on growth and flowering in Lolium Temulentum. Phytochemistry 1998, 49, 1509.
10. Mander, L. N.; Camp, D.; Evans, L. T.; King, R. W.; Pharris, R. P.; Sherburn, M.; Twitchin, B. Designer gibberellins: the quest for specific activity. Acta Horticulturae 1995, 394, 45.
11. Camp, D.; Hanson, G. R.; Jenkins, I. D. Formation of radicals in the Mitsunobu reaction. J. Org. Chem. 1995, 60, 2977.
12. Blount, J. F.; Camp, D.; Hart, R. D.; Healy, P. C.; Skelton, B. W.; White, A. H. The synthesis and structural characterization of mesityldiphenylphosphine, dimesitylphenylphospine and trimesitylphosphine. Aust. J. Chem. 1994, 47, 1631.
13. Bowen, R. J.; Camp, D.; Effendy; Healy, P. C.; Skelton, B. W.; White, A. H. Structural and solid state ³¹P NMR studies of tetrameric 1:1 butyldiphenylphospine complexes of silver (I) halides. Aust. J. Chem. 1994, 47, 693.
14. Camp, D.; Jenkins, I. D. The mechanism of the Mitsunobu esterification reaction. 3. The use of tributylphosphine. Aust. J. Chem. 1992, 45, 47.
15. Baker, L.-J.; Bowmaker, G. A.; Camp, D.; Effendy; Healy, P. C.; Schmidbaur, H.; Steigelmann, O.; White, A. H. Structural, far-IR and ³¹P NMR studies of two-coordinate complexes of tris(2,4,6-trimethoxyphenyl) phosphine with silver (I) halides. Inorg. Chem. 1992, 31, 3656.
16. Bowmaker, G. A.; Camp, D.; Hart, R. D.; Healy, P. C.; Skelton, B. W.; White, A. H. Comparative structural studies on three-coordinate copper (i) halide complexes with tertiary phosphines. Crystal structures of [(PPh₂Mes)CuX₂] and [(PPhMes₂)CuX]₂ (Mes=Mesityl; X=C1, Br; 1). Aust. J. Chem. 1992, 45, 1155.
17. Camp, D.; Healy, P. C.; Jenkins, I. D.; Skelton, B. W.; White, A. H. The reaction of diphenylphosphine with dialkyl azodicarboxylates. J. Chem. Soc. Perkin Trans. 1. 1991, 1323.
18. Camp, D.; Jenkins, I. D. The reaction of thiols and α,ω-dithiols with triphenylphosphine and diisopropyl azodicarboxylate. Aust. J. Chem. 1990, 43, 161.
19. Camp, D.; Jenkins, I. D. Mechanism of the Mitsunobu esterification reaction. 1. The involvement of phosphoranes and oxyphosphonium salts. J. Org. Chem. 1989, 54, 3045.
20. Camp, D.; Jenkins, I. D. Mechanism of the Mitsunobu esterification reaction. 2. The involvement of (acyloxy)alkoxyphosphoranes. J. Org. Chem. 1989, 54, 3049.
21. Camp, D.; Jenkins, I. D. The use of a phosphine containing a basic group in the Mitsunobu esterification reaction. Aust. J. Chem. 1988, 41, 1835.