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Автор DinsmorePresent address: Department of Chemistry, University of Witwatersrand, PO WITS 2050, South Africa., Andrew
Автор DoylePresent address: BioFocus plc, 130 Abbott Drive, Sittingbourne Research Centre, Sittingbourne, Kent, UK ME9 8AZ., Paul M.
Автор Young, Douglas W.
Дата выпуска 2001
dc.description (2S)-2-Amino-3-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)propionic acid 8, an isomer of the natural product willardiine 7, was synthesised by treatment of the pyroglutamate urea 19 with mild base followed by deprotection in a two-step modification of our â ring-switchingâ approach to the synthesis of glutamate antagonists. Use of this two-step strategy has allowed us to synthesise l-alanine derivatives, which are β-substituted by a reduced pyrimidinedione which contains a second chiral centre. In one case, the antagonist activity at metabotropic glutamate receptors of two diastereoisomers showed little difference.
Формат application.pdf
Издатель Royal Society of Chemistry
Название Use of a modified ring-switching strategy to synthesise the glutamate antagonist (2S)-2-amino-3-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)propionate and related compounds with two chiral centres1
Тип research-article
DOI 10.1039/b109820a
Electronic ISSN 1364-5463
Print ISSN 0300-922X
Журнал Journal of the Chemical Society, Perkin Transactions 1
Первая страница 155
Последняя страница 164
Аффилиация DinsmorePresent address: Department of Chemistry, University of Witwatersrand, PO WITS 2050, South Africa. Andrew; Sussex Centre for Biomolecular Design and Drug Development, University of Sussex
Аффилиация DoylePresent address: BioFocus plc, 130 Abbott Drive, Sittingbourne Research Centre, Sittingbourne, Kent, UK ME9 8AZ. Paul M.; Sussex Centre for Biomolecular Design and Drug Development, University of Sussex
Аффилиация Young Douglas W.; Sussex Centre for Biomolecular Design and Drug Development, University of Sussex
Выпуск 2
Библиографическая ссылка A. Dinsmore, P. M. Doyle, P. B. Hitchcock, D. W. Young, Part of this work has been published in preliminary form in , Tetrahedron Lett., 2000, 41, 10153
Библиографическая ссылка G. K. Steinberg, J. Saleh, D. Kunis, R. DeLaPaz, S. R. Zarnegar, Stroke, 1989, 20, 1247
Библиографическая ссылка T. A. Johansen, K. Frydenvang, B. Ebert, P. Krogsgaard-Larsen, U. Masden, See , J. Med. Chem., 1994, 37, 3252, and references cited therein
Библиографическая ссылка A. N. Bowler, A. Dinsmore, P. M. Doyle, D. W. Young, J. Chem. Soc., Perkin Trans. 1, 1997, 1297
Библиографическая ссылка R. H. Evans, A. W. Jones, J. C. Watkins, J. Physiol., 1980, 308, 71P
Библиографическая ссылка H. Sugiyama, M. Watanabe, H. Taji, Y. Yamamoto, I. Ito, Neurosci. Res., 1989, 7, 164
Библиографическая ссылка R. A. August, J. A. Khan, C. M. Moody, D. W. Young, J. Chem. Soc., Perkin Trans. 1, 1996, 507
Библиографическая ссылка S. J. East, J. Garthwaite, Eur. J. Pharmacol., 1992, 219, 395

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