Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Herbert J. Brabander"'
Autor:
Gerardo D. Francisco, Herbert J. Brabander, Richard M. Mangano, Richard H. Kramss, Eugene J. Trybulski
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 2:827-832
The synthesis and radioligand binding data of optically active hydroxylated oxotremorine derivatives are described. These are significant pharmacological differences between the enantiomers, most notably at the 3- and 4-position of the pyrrolidinone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92eafcabe8e94b74a2f7c683c87551b3
https://doi.org/10.1016/s0960-894x(00)80539-9
https://doi.org/10.1016/s0960-894x(00)80539-9
Publikováno v:
Journal of Heterocyclic Chemistry. 24:837-843
2-Aminobenzimidazoles were reacted with enaminones in acetic acid to give pyrimido[1,2-a]benzimidazoles. With a substituted enaminone only one regioisomer was obtained. Structural assignments based on nmr and uv spectroscopy are presented. Possible p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::703358f3f37e48619a5bf62e5305da35
https://doi.org/10.1002/jhet.5570240357
https://doi.org/10.1002/jhet.5570240357
Autor:
Arnold C. Osterberg, F. M. Lovell, Thomas C. McKenzie, Herbert J. Brabander, Corris M. Hofmann, D. B. Cosulich, Epstein Joseph William, Sidney R. Safir, William J. Fanshawe
Publikováno v:
Journal of Medicinal Chemistry. 24:481-490
A series of 1-aryl-3-azabicyclo[3.1.0]hexanes was synthesized by hydride reduction of 1-arylcyclopropanedicarboximides. Hydroxyphenyl analogues 20, 22, and 24 were prepared by EtSNa--DMF ether cleavage of the corresponding methoxyphenyl analogues 2m,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24186b6030bea4a989617f1811413125
https://doi.org/10.1021/jm00137a002
https://doi.org/10.1021/jm00137a002
Publikováno v:
The Journal of Organic Chemistry. 26:4057-4060
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::500b590274e098f5a7a457098e684f25
https://doi.org/10.1021/jo01068a099
https://doi.org/10.1021/jo01068a099
Publikováno v:
The Journal of Organic Chemistry. 26:2120-2123
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87eb741e58ef6fa1dc01b71bc5764d1f
https://doi.org/10.1021/jo01065a618
https://doi.org/10.1021/jo01065a618
Publikováno v:
Journal of the American Chemical Society. 81:5637-5640
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1a4c8ffcdf46f45c022db812a596304
https://doi.org/10.1021/ja01530a029
https://doi.org/10.1021/ja01530a029
Publikováno v:
The Journal of Organic Chemistry. 26:4051-4057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1530088634776cf027dfead19dcca6b
https://doi.org/10.1021/jo01068a098
https://doi.org/10.1021/jo01068a098
Publikováno v:
Journal of Medicinal Chemistry. 9:852-857
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c0f4730b28a8b4b79f9404e04ecd6f4
https://doi.org/10.1021/jm00324a017
https://doi.org/10.1021/jm00324a017
Publikováno v:
Journal of Heterocyclic Chemistry. 2:130-135
The synthesis of 8-tert-aminoalkoxy-6-aryl-6,7-diazaspiro[3.4]oct-7-en-5-ones (1) and 6-tert-aminoalkyl-7-aryl-6,7-diazaspiro[3.4]octane-5,8-diones has been accomplished. Two synthetic methods are described, each of which yields principally one isome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3dd9127ff4ad8ced504060820e91c44
https://doi.org/10.1002/jhet.5570020204
https://doi.org/10.1002/jhet.5570020204
Publikováno v:
The Journal of Organic Chemistry. 26:485-490
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8276352ce946cf860d68344c561db300
https://doi.org/10.1021/jo01061a049
https://doi.org/10.1021/jo01061a049