Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Janet M. Gillam"'
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 53:1521-1525
The 1H and 13C NMR chemical shifts of substituted 1,4-dephenyl-2-butene-1,4-diones indicate that these compounds in CDCl3 solution exist mainly in the s-trans-s-trans (Z) keto (trans Z) configuration and that hydrogen bonding between the NH proton an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fedd65d8027fc1496d54fc6f637cb49d
https://doi.org/10.1016/s1386-1425(97)00061-9
https://doi.org/10.1016/s1386-1425(97)00061-9
Autor:
Ray Stepney, Paul Leff, M.L. Bolofo, Alan McNeill, Paul Barraclough, C. John Harris, Alan D. Robertson, Janet M. Gillam, Brendan J. R. Whittle, Heather Giles, Michael G. Kelly
Publikováno v:
Bioorganic & Medicinal Chemistry. 4:81-90
The rationale for investigating conformationally restricted analogues of BW245C as DP-receptor ligands and the syntheses of three such racemic bicyclic imidazolidinone analogues are described. Compounds 7 (BW587C), 8 (BW480C85), and 9 (BW572C85) were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c96594a9666673275121ccee2d38cd9b
https://doi.org/10.1016/0968-0896(95)00173-5
https://doi.org/10.1016/0968-0896(95)00173-5
Publikováno v:
Journal of Magnetic Resonance, Series B. 109:275-283
A new method for measuring and assigning long-range 1 H– 13 C spin coupling constants is presented. This is based on the HSQC pulse sequence with substitution of the 180° 1 H pulse by a selective 180° 1 H pulse and a 180° 13 C pulse in the middl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a95f7b132ddf797771130b0d7046252
https://doi.org/10.1006/jmrb.1995.9994
https://doi.org/10.1006/jmrb.1995.9994
Autor:
V. Paul Gerskowitch, David Cambridge, Mark V. Whiting, Janet M. Gillam, Robert Antony David Hull, Paul Barraclough, Steven Smith, Shah Gita Punjabhai, Ramachandran Iyer, Heather Giles, P. Randall, Robert C. Glen, James W. Black, David Firmin
Publikováno v:
Archiv der Pharmazie. 325:225-234
Aryl substituted 1H-imidazo[1, 2-a]imidazole 8, imidazo[2,1-b]thiazole 9, 1,4-dihydroimidazo[4,5-d]imidazole 11, and 1(2),4-dihydroimidazo[4,5-c]pyrazoles 12–17 have been prepared. An X-ray crystallographic study confirmed the structure of 8 and sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cea692c4fc32e06c8963b295c1aebe9
https://doi.org/10.1002/ardp.19923250407
https://doi.org/10.1002/ardp.19923250407
Autor:
Paul N. Sanderson, Paul Barraclough, John C. Lindon, Steven Smith, David Firmin, Janet M. Gillam, Malcolm S. Nobbs
Publikováno v:
Magnetic Resonance in Chemistry. 29:468-475
The pKa, values of six sulmazole analogues were measured spectrophotometrically. The major protonation sites for most of these bridgehead nitrogen heterocycles were determined by 1H and 13C NMR methods. The aryl-substituted imidazo[1,2-a]pyrimidine (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eacd62caa0131489d52e9364ee5dde9
https://doi.org/10.1002/mrc.1260290511
https://doi.org/10.1002/mrc.1260290511