Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Nigel J. Barnes"'
1
The Design and Synthesis of Inhibitors of Imidazoleglycerol Phosphate Dehydratase as Potential Herbicides
Autor: Timothy Robert Hawkes, Russell Martin Ellis, Paul R. Davies, Peter A. Walker, Andrew J. Knee, Roger Barrett, Terence Lewis, John Cox, Sally Russell, Nigel J. Barnes, Peter Bellini, Joseph John Swanborough
Publikováno v: Pesticide Science. 50:297-311
The discovery and exploration of a new class of broad-spectrum post-emergent herbicides with a novel mode of action, namely the disruption of histidine biosynthesis via inhibition of imidazoleglycerol phosphate dehydratase (IGPD; E.C. 4.2.1.19), are
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0a2c92e1f86ad18eb65491573fcf8062
https://doi.org/10.1002/(sici)1096-9063(199708)50:4<297::aid-ps592>3.0.co
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2
Synthesis of 2-deoxy-α- and -β-D-arabino-hexopyranosyl phosphonic acids and related compounds; analogues of early intermediates in the shikimate pathway
Autor: Richard H. Wightman, Mark A. Probert, Nigel J. Barnes
Publikováno v: J. Chem. Soc., Perkin Trans. 1. :431-438
Treatment of 1-O-acetyl-3,4,6-tri-O-benzyl-2-deoxy-D-arabino-hexopyranose 18 with trimethyl phosphite in the presence of trimethylsilyl triflate gave a separable mixture of dimethyl (3,4,6-tri-O-benzyl-α-D-arabino-hexopyranosyl)phosphonate 19 (35%)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3beff02d202317407ef14b541fef0fc7
https://doi.org/10.1039/p19960000431
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3
ChemInform Abstract: Synthesis of 2-Deoxy-α- and -β-D-arabino-hexopyranosyl Phosphonic Acids and Related Compounds; Analogues of Early Intermediates in the Shikimate Pathway
Autor: Nigel J. Barnes, Mark A. Probert, Richard H. Wightman
Publikováno v: ChemInform. 27
Treatment of 1-O-acetyl-3,4,6-tri-O-benzyl-2-deoxy-D-arabino-hexopyranose 18 with trimethyl phosphite in the presence of trimethylsilyl triflate gave a separable mixture of dimethyl (3,4,6-tri-O-benzyl-α-D-arabino-hexopyranosyl)phosphonate 19 (35%)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d56ad8f89285ea133ab4c8616a950974
https://doi.org/10.1002/chin.199624220
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7
The synthesis of optically active tetrahydropyrans by the addition of a stabilised Witting reagent to pyranose sugars
Autor: Garry Procter, Nigel J. Barnes, Alan Hornsby Davidson, Leslie Richard Hughes
Publikováno v: Journal of the Chemical Society, Chemical Communications. :1292
The addition of the phosphonate–sulphone (8) to the carbohydrates (9) and (10) gave the tetrehydropyrans (11) and (12) as mixtures of α- and β-isomers; treatment of the mixture with sodium hydride gave the purer β-isomers.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6d221f952ee2a354dad70164117a5f66
https://doi.org/10.1039/c39850001292
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