Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Robert K. Husa"'
Publikováno v:
Tetrahedron. 55:11787-11802
A racemic synthesis of azanoradamantane (±) -3 was accomplished via Yamamoto's MAD-catalyzed Diels-Alder protocol. Subsequently, a scalable asymmetric synthesis of azanoradamantane benzamide SC-52491 was carried out employing Helmchen's asymmetric D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73c3925ad6f7b73fe3b28524f8e6e92f
https://doi.org/10.1016/s0040-4020(99)00680-8
https://doi.org/10.1016/s0040-4020(99)00680-8
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c119257e8c4955fb0e2380f48f3fda50
https://doi.org/10.1002/chin.199218265
https://doi.org/10.1002/chin.199218265
Autor:
J.‐P. Vanhoeck, Michael F. Rafferty, M. Reichman, Shashidhar N. Rao, M A Savage, Timothy J. Hagen, Robert K. Husa, E. A. Hallinan, Awilda Stapelfeld, Sofya Tsymbalov
Publikováno v:
ChemInform. 25
8-Chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-acetylhydrazide (1, SC-19220) has been previously reported by us and others to be a PGE2 antagonist selective for the EP1 receptor subtype with antinociceptive activities. Analogs of SC-192
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fa9e44c870fc553bcb212af542b9b5f
https://doi.org/10.1002/chin.199411197
https://doi.org/10.1002/chin.199411197
Publikováno v:
Journal of the American Chemical Society. 113:9820-9824
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efff09b0eceaabf148457acc0084c6ec
https://doi.org/10.1021/ja00026a016
https://doi.org/10.1021/ja00026a016
Autor:
Shashidhar N. Rao, M. Reichman, E. A. Hallinan, Awilda Stapelfeld, M A Savage, Michael F. Rafferty, Sofya Tsymbalov, Robert K. Husa, J.‐P. Vanhoeck, Timothy J. Hagen
Publikováno v:
Scopus-Elsevier
8-Chlorodibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 2-acetylhydrazide (1, SC-19220) has been previously reported by us and others to be a PGE2 antagonist selective for the EP1 receptor subtype with antinociceptive activities. Analogs of SC-192
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94146940fd94b5b192b92d32b31e5af4
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027424447&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027424447&partnerID=MN8TOARS
