Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Haydn W. R. Williams"'
Autor:
John Scheigetz, Jeffrey D. Chambers, Claude Dufresne, Haydn W. R. Williams, Cheuk K. Lau, Michael A. Bernstein, Jason Crawford
Publikováno v:
ChemInform. 24
Thermolysis of 1-phenyl-4H-1,3,2-benzodioxaborins generated the corresponding ortho-quinone methides, which were found to undergo intermolecular cycloaddition reactions with ethyl vinyl ether, dihy...
Autor:
M. Belley, Eugene G. Herold, Marc Labelle, Kathleen M. Metters, E. Grimm, Helene Perrier, Y. B. Xiang, Robert N. Young, D.H. Patrick, Patrick Roy, Lau Cheuk-Kun, John G. DeLuca, Anthony W. Ford-Hutchinson, Daniel Guay, L. Charette, E. Champion, P. Masson, H. Piechuta, A. Lord, Serge Leger, Thomas R. Jones, Jacques-Yves Gauthier, Petpiboon Prasit, Robert Zamboni, Nathalie Ouimet, Yves Leblanc, Claude Dufresne, C.B. Pickett, Zhaoyin Wang, Scott J. Grossman, Richard Frenette, C. S. Mcfarlane, M. McAuliffe, Haydn W. R. Williams, Marc Blouin
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 2:1141-1146
A new, potent, orally active leukotriene D 4 receptor antagonist has been discovered. The structure -activity relationship leading to L-695,499 is described.
Autor:
John Scheigetz, Claude Dufresne, Haydn W. R. Williams, Jeffrey D. Chambers, Cheuk K. Lau, Michael A. Bernstein, Jason Crawford
Publikováno v:
Canadian Journal of Chemistry. 70:1717-1732
Thermolysis of 1-phenyl-4H-1,3,2-benzodioxaborins generated the corresponding ortho-quinone methides, which were found to undergo intermolecular cycloaddition reactions with ethyl vinyl ether, dihydropyran, β-methylstyrene, cyclohexene, and 1-ethoxy
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 28:297-306
The synthesis of 5-[3-{2-(7-chloroquinolin-2-yl)ethenyl}-phenyl]-8-dimethylcarbamyl-4,6-[6-35S]dithiaoctanoic acid at a specific activity of 1350 Ci/mmol is reported. This compound is a reagent suited for selective affinity binding studies at the LTD
Autor:
Robert Zamboni, Haydn W. R. Williams, Michael A. Bernstein, Robert N. Young, Kathleen M. Metters
Publikováno v:
Bioorganic Chemistry in Healthcare and Technology ISBN: 9781468413564
Leukotrienes D4 (1a) and E4 (1b) are potent contractile substances which have been implicated in the ethiology of human asthma. These leukotrienes exert their effects through interaction with specific receptors on pulmonary smooth muscle and other ti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a076b745df83d626b230c468e08cb111
https://doi.org/10.1007/978-1-4684-1354-0_37
https://doi.org/10.1007/978-1-4684-1354-0_37
Autor:
Claude Dufresne, Patrice C. Belanger, Sylvie Tardiff, Cheuk K. Lau, Haydn W. R. Williams, John Scheigetz
Publikováno v:
ChemInform. 21
Reaction of a phenol with an aldehyde in the presence of phenylboronic acid gives a 1,3,2-benzodioxaborin. The latter could be reduced to the corresponding ortho-alkylphenol with tert-butylamine borane in the presence of aluminum chloride. Alternativ
Publikováno v:
Canadian Journal of Chemistry. 53:2279-2292
A series of 3-substituted-aminomethy1-3-hydroxy-3,4-dihydro-2H-1,5-benzodioxepins is described. Members of the series constitute a unique class of β-adrenergic stimulants and possess interesting bronchial dilator activity.
Autor:
Haydn W. R. Williams
Publikováno v:
Canadian Journal of Chemistry. 54:3377-3382
The syntheses of 2-isopropylamino-1-(5-hydroxy-4H-pyran-4-on-2-yl)ethanol and the corresponding 4-pyridone and 1-methyl-4-pyridone analogues are described. The selective reduction of an aliphatic nitro group in the presence of a benzyl ether linkage
Publikováno v:
Canadian Journal of Chemistry. 61:1383-1386
The resolution of 2-tetrahydrofuran-carboxylic acid and assignment of configuration to the enantiomers are reported. New syntheses of the enantiomers of 2-tetrahydrofurancarboxaldehyde are also described.
Publikováno v:
Journal of Heterocyclic Chemistry. 13:841-844
The syntheses of some 1,8-naphthyridines substituted in the 6-position with heterocyclic groups are described. A synthetic route to 6-amino-5,7-dimethyl-1,8-naphthyridin-2(1H)one is also presented.