Zobrazeno 1 - 10
of 14
pro vyhledávání: '"G. J. Ellames"'
Autor:
I. Shaw, V. L. Murrell, L. P. Kingston, P. W. Miller, A. Burgos, F. Le Strat, M. H. F. Pedersen, William J. S. Lockley, S. Twiddy, Sean L. Kitson, S. L. Kostiuk, M. J. Hickey, S. Schou, M. Sriram, R. S. Sharma, S. Husbands, L. Nanson, L. E. Jennings, C. Plisson, R. Sherhod, S. Kealey, R. T. Brown, R. Bragg, David C. Harrowven, A. Kohler, A. J. P. White, J. Tate, A. D. Gee, T. Woodcock, A. H. McNeill, N. J. Long, N. Bushby, J. M. Herbert, M. L. Clarke, J. R. Harding, M. Jones, D. J. Wilkinson, T. S. Moody, M. Tredwell, Mark E. Light, G. J. Ellames, K. G. Pinney, D. Killick, P. H. Allen, V. Gouverneur, Traci Smith, William Watters, L. F. Dudin, A. J. Bloom
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 54:387-398
The 19th annual symposium of the International Isotope Society's United Kingdom Group took place at the Wellcome Genome Campus, Hinxton, Cambridge, UK on Thursday 14th October 2010. The meeting was attended by around 80 delegates from academia and in
Autor:
G. Åberg, F. I. Aigbirhio, E. Alexakis, N. Al-Maharik, M. Almi, Y. Ambacher, S. Andersson, A. Athlan, G. Badman, S. A. Baldwin, M. Baumann, I. R. Baxendale, N. P. Botting, R. A. Bragg, J. A. Brown, A. Burton, N. Bushby, K. Cable, G. Campbell, R. Carr, M. Carroll, L. Chen, M. Christlieb, P. Davies, G. J. Ellames, W. Ellis, C. Elmore, T. Fryatt, N. Geach, J. R. Harding, S. Hartmann, S. Harwood, J. J. Hayward, P. J. F. Henderson, R. B. Herbert, J. R. Heys, S. Hölzl, M. D. Hopkin, P. Horn, T. Ilyas, S. Irvine, S. D. Jackson, J. Jin, A. Keats, A. R. Kennedy, W. J. Kerr, M. O. Kitching, C. Landreau, S. Lanners, R. Lawrence, K. W. M. Lawrie, S. V. Ley, G. Little, W. J. S. Lockley, D. Maier, C. Manning, A. McNeill, D. A. Middleton, S. Montgomery, J. J. Morrison, L. Mrzljak, J. Newman, J. Newsome, N. Nikbin-Roudsari, G. N. Nilsson, M. F. Oldfield, S. G. Patching, D. J. Procter, G. Randall, A. A. Robertson, C. S. Rummel, D. Rustidge, R. Sherhod, N. Shipley, C. D. Smith, C. J. Smith, D. I. Smith, C. Song, L. Tamborini, I. Waterhouse, A. Watts, J. L. Werkheiser, G. Williams, C. L. Willis, P. Woodward, R. Yan, G. Young, Q. Zhang
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 51:247-261
Autor:
V. Snieckus, N. J. Geach, G. P. Randall, C. J. Winfield, A. Studer, A. C. Spivey, T. Jones, C. Noban, G. J. Ellames, A. Kohler, H. Wadsworth, J. Rieke-Zapp, S. Stone-Elander, J. Goehl, B. Perry, J. Windels, M. H. Marx, J. Krüger, B. Manmontri, G. Fels, F. Wüst, T. Kniess, R. Bergmann, P. Mäding, F. Füchtner, C. S. Hilger, M. Halks-Miller, R. Horuk, L. Matei, C. Postolache, V. Fugaru, E. Condac, A. Dinischiotu, M. Costache, J. Atzrodt, V. Derdau
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 47:1035-1060
V Snieckus [Queen's University, Canada]—The Directed Ortho Metalation—Cross Coupling Symbiosis in Aromatic Synthesis. N Geach, GP Randall, CJ Winfield [Scynexis, UK]—Isotopically Labelled 4-Formylimidazole. A Studer [Marburg University, Germany
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2439-2442
A novel aldolase from Streptomyces amakusaensis which catalyses a reverse aldol reaction on (2S,3R)-β-hydroxy-α-amino acids is specific for aromatic compounds, but otherwise shows broad substrate tolerance. This is further illustrated by its abilit
Publikováno v:
Canadian Journal of Chemistry. 72:114-117
A unique aldolase, which was isolated from Streptomyces amakusaensis, is used to catalyse a reverse aldol reaction on representative racemic β-hydroxy-α-amino acids (3–6) to give samples of the (2R,3S)-(D-threo)-enantiomers with excellent enantio
Autor:
Anthony P. Metters, Kevin Robert Lawson, Roger Munro Upton, William R. McKay, Jon P. Dickens, Anthony M. S. Pope, G. J. Ellames, Nigel J. Hare, Peter L. Myers
Publikováno v:
ChemInform. 22
1-(2,4-Dichlorophenyl)-2-phenylpropen-1-one (2) is identified as a potent antibacterial agent. A compound, 2-chloro-1-(2,4-dichlorophenyl)-3-(1H-imidazol-1-yl)-2-phenylpropan++ +-1-one (5) has been designed with the intention of its acting as a pro-d
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 25
A unique aldolase, which was isolated from Streptomyces amakusaensis, is used to catalyse a reverse aldol reaction on representative racemic β-hydroxy-α-amino acids (3–6) to give samples of the (2R,3S)-(D-threo)-enantiomers with excellent enantio
Publikováno v:
ChemInform. 28
A novel aldolase from Streptomyces amakusaensis which catalyses a reverse aldol reaction on (2S,3R)-β-hydroxy-α-amino acids is specific for aromatic compounds, but otherwise shows broad substrate tolerance. This is further illustrated by its abilit
Publikováno v:
Synfacts. 2010:0115-0115