Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ronald F. Cookson"'
Publikováno v:
PharmacoEconomics. 14:285-297
Objective:We constructed a UK-based decision model of palliative care for terminally ill cancer patients who were switched from a weak to a strong opioid so that the expected direct healthcare costs in the UK could be estimated from the time a patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a69e5d1fd4441e702e0979c643239bf8
https://doi.org/10.2165/00019053-199814030-00005
https://doi.org/10.2165/00019053-199814030-00005
Autor:
Ronald F Cookson, Krista F Huybrechts
Publikováno v:
Journal of Medical Economics. 1:103-134
SummaryA variety of economic studies have been carried out in Europe, North America and Australia. Risperidone is dominant over haloperidol, providing both an improvement in patient benefit and decreasing direct medical costs. These effects are most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ceafba76aa883db50ad1ec08b07cf42
https://doi.org/10.3111/199801103134
https://doi.org/10.3111/199801103134
Publikováno v:
Organic Mass Spectrometry. 13:341-343
A combination of electron impact, chemical ionization, field desorption and field ionization mass spectrometry has been employed to demonstrate that the LAH reduction product of 3H-1,2-benzodithiole-3-thione is the dimer, dibenzo[c,h]-3H,10H-dihydro-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dd89db5d3d0311cc85c25473f3fce7a
https://doi.org/10.1002/oms.1210130609
https://doi.org/10.1002/oms.1210130609
Autor:
Ronald F. Cookson, Alan C. Richards
Publikováno v:
Chemischer Informationsdienst. 5
1,2,5-Thiadiazole, previously thought to be resistant to electrophilic substitution, has been shown to undergo chloromethylation; N-chlorosuccinimide is more selective than N-bromosuccinimide in the dihalogenation of 3,4-dimethyl-1,2,5-thiadiazole.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec40806fefe8ed2f2213f31ae3b910d9
https://doi.org/10.1002/chin.197447296
https://doi.org/10.1002/chin.197447296
Publikováno v:
Chemischer Informationsdienst. 6
Treatment of the phenacyl quaternary salts of isoquinoline and quinoline with ammonium acetate in acetic acid gave the products (5) and (7) respectively, and not those previously reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::305cfd810fda996191ddface3412adec
https://doi.org/10.1002/chin.197506270
https://doi.org/10.1002/chin.197506270
Autor:
RONALD F. COOKSON, RONALD E. RODWAY
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19142bd994002d2b1b1883668652a429
https://doi.org/10.1002/chin.197552245
https://doi.org/10.1002/chin.197552245
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :201
Treatment of 2-phenacylisoquinolinium bromide with ammonium acetate in acetic acid gave 5,10-dihydro-2-phenylimidazo[1,2-b]isoquinoline (4) by cyclisation at the 3-position of the isoquinoline ring. The mechanism of this reaction is discussed. On sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6c69aa75ec4239e0190b51b951e6a6b
https://doi.org/10.1039/p19760000201
https://doi.org/10.1039/p19760000201
Autor:
Ronald F. Cookson, Ronald E. Rodway
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1854
Heating 2-aminoethylammonium tosylate (EDMT) with various aromatic bicyclic amides at 200–250 °C provides a convenient single-stage synthesis of the corresponding dihydroimidazo-compounds. The procedure worked well with phthalazinones (1), quinolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2614b5040c73cf9389749670dc8b035
https://doi.org/10.1039/p19750001854
https://doi.org/10.1039/p19750001854
Autor:
Ronald F. Cookson, Ronald E. Rodway
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1850
Phenanthridone reacts with 2-aminoethylammonium tosylate at 200–250 °C to give 2,3-dihydroimidazo[1,2-f]-phenanthridine (2; R = H) in high yield. This reaction could not be extended to the monotosylate salts of o-phenylenediamine, propane-1,3-diam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efc366a3758aeed30cdcd752814f451a
https://doi.org/10.1039/p19750001850
https://doi.org/10.1039/p19750001850
Autor:
Alan C. Richards, Ronald F. Cookson
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :585
1,2,5-Thiadiazole, previously thought to be resistant to electrophilic substitution, has been shown to undergo chloromethylation; N-chlorosuccinimide is more selective than N-bromosuccinimide in the dihalogenation of 3,4-dimethyl-1,2,5-thiadiazole.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7ef07fea1ab1d728f72384f58c934b6
https://doi.org/10.1039/c39740000585
https://doi.org/10.1039/c39740000585