Zobrazeno 1 - 10
of 737
pro vyhledávání: '"G. W. H. Cheeseman"'
Autor:
Edward F. Lasala
Publikováno v:
Journal of Pharmaceutical Sciences. 66:1062
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba9c7fb58d24249be338f367581fe68d
https://doi.org/10.1002/jps.2600660752
https://doi.org/10.1002/jps.2600660752
Autor:
LaSala, Edward F.
Publikováno v:
Journal of Pharmaceutical Sciences; July 1977, Vol. 66 Issue: 7 p1062-1062, 1p
Autor:
LaSala, Edward F.
Publikováno v:
In Journal of Pharmaceutical Sciences July 1977 66(7):1062-1062
Autor:
R. F. Cookson, G. W. H. Cheeseman
Publikováno v:
Chemistry of Heterocyclic Compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb18f70979e530517a0876987462bef5
https://doi.org/10.1002/9780470187333.ch29
https://doi.org/10.1002/9780470187333.ch29
Publikováno v:
Journal of Heterocyclic Chemistry. 22:423-427
Synthese de dihydro-6,7 pyrrolo [1,2-a] benzothiadiazocine-3,1,6ones-6 par cyclisation intramoleculaire des thiols provenant de la reduction par NaBH 4 de chloro-2″ acylamino-2'- ou [bromo-2″ ethyl tosyl amino]-2' phenyl-1 thiocyanato-2 pyrroles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8682fbac3b925bec7f54f62da8abc765
https://doi.org/10.1002/jhet.5570220241
https://doi.org/10.1002/jhet.5570220241
Publikováno v:
Organic Magnetic Resonance. 8:357-360
13C n.m.r. chemical shifts and carbon-proton coupling constants of 2-substituted pyrimidines are reported. The carbon chemical shifts are correlated with π-electron densities. Substituents which cause deshielding at the directly bound carbon (e.g. N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65c78c6f08162c9208e730d44055c386
https://doi.org/10.1002/mrc.1270080707
https://doi.org/10.1002/mrc.1270080707
Autor:
C. J. Turner, G. W. H. Cheeseman
Publikováno v:
Organic Magnetic Resonance. 6:663-666
Carbon-13 NMR chemical shifts and one-bond carbon–hydrogen coupling constants have been obtained at 15·09 MHz. The trends in the carbon chemical shifts obtained for the pyrazines parallel those of monosubstituted benzenes and 2-substituted pyridin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::507efdab40a938500d1ed314ce938acd
https://doi.org/10.1002/mrc.1270061212
https://doi.org/10.1002/mrc.1270061212
Autor:
George Varvounis, G. W. H. Cheeseman
Publikováno v:
Journal of Heterocyclic Chemistry. 24:1157-1161
A new synthesis of the thiadiazocine ring is reported together with an investigation of the diverse chemical reactions of pyrrolo[1,2-a][3,1,6]benzothiadiazocines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61688afa2a122929b0166c095b5794dc
https://doi.org/10.1002/jhet.5570240445
https://doi.org/10.1002/jhet.5570240445
Autor:
G. W. H. Cheeseman, S. G. Greenberg
Publikováno v:
Journal of Heterocyclic Chemistry. 16:241-244
The title compounds are. Prepared by the reaction of carbonyl compounds with 1-(2′-amino-methylphenyl)pyrrole hydrochloride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b5734136b1d852368f14f98a9091423
https://doi.org/10.1002/jhet.5570160209
https://doi.org/10.1002/jhet.5570160209
Publikováno v:
Tetrahedron. 33:2255-2258
The intramolecular cyclization of the tertiary amines ( 3 ) with potassium amide in liquid ammonia affords a variety of unsymmetrical isoindolines ( 5 ) and isoindoles ( 6 ).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6603b8aa8835cd25049a56ff0f97213
https://doi.org/10.1016/0040-4020(77)80012-4
https://doi.org/10.1016/0040-4020(77)80012-4