Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Norman W. Gilman"'
Autor:
Norman W. Gilman, Louis J. Todaro, James Valentine Earley, John F. Blount, Perry Rosen, Charles M. Cook
Publikováno v:
The Journal of Organic Chemistry. 58:3285-3298
The resolution of the 1-tert-butylimidazo[1,5-a] [1,4]benzodiazepines 12, 25, and 31 is described. These compounds do not contain a center of symmetry but exist as conformational isomers due to the presence of a chiral plane. The resolution was carri
Autor:
Perry Rosen, Louis J. Todaro, Charles M. Cook, John F. Blount, Norman W. Gilman, James Valentine Earley
Publikováno v:
ChemInform. 24
Publikováno v:
Journal of the American Chemical Society. 112:3969-3978
Publikováno v:
ChemInform. 21
Autor:
B. C. Holland, Norman W. Gilman
Publikováno v:
Synthetic Communications. 4:199-202
A recent communication by Brattesani and Heathcock1 on the alkylation of acetylenes with alkyl halides in hexamethylphosphoramide (HMPA) prompts us to report our work which is of a similar nature. We were interested in preparing acetylenic acids of f
Publikováno v:
Bioelectrochemistry and Bioenergetics. 16:407-426
A novel mechanism for BZ action is proposed in which a BZ is protonated by GABA or protein RNH3+ to yield an iminium species that is responsible for drug activity via charge transfer (c.t.). The following evidence from our work and prior studies supp
Autor:
James V. Earley, Norman W. Gilman
Publikováno v:
Synthetic Communications. 15:1271-1276
Publikováno v:
Journal of Heterocyclic Chemistry. 14:1163-1169
The syntheses of novel 8-chloropyrazolo[1,5-a][1,4]benzodiazepines and of an imidazo-benzodiazepinone utilizing products from the nucleophilic substitution of fluorine in 2-fluoro-5-nitrobenzophenone (1) by pyrazole-3,5-dicarboxylic acid, dimethyl es
Nucleophilic displacement of aromatic fluorine. Part V. Use of nitrogen heterocycles as nucleophiles
Publikováno v:
Journal of Heterocyclic Chemistry. 14:1157-1162
The scope of the nucleophilic displacement of aromatic halogens on 1,4-benzodiazepine precursors by the anions of pyrroles, pyrazoles and imidazoles was studied both with and without electron-withdrawing substitutents on the heterocyclic nucleophiles
Publikováno v:
Journal of Heterocyclic Chemistry. 23:119-124
The synthesis of eight pyridazino[1,6-a]benzimidazoles by a novel synthetic route is described. This relatively unexplored heterocyclic ring system is readily accessible starting from benzoylpropionic acids and phenylhydrazines in five steps. The int