Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Edvige Galeazzi"'
Autor:
Roger L. Whiting, Rosenkranz Roberto P, Joseph M. Muchowski, Joan M. Caroon, Mcclelland Deborah L, Richard M. Eglen, Robin D. Clark, Lawrence E. Fisher, Anton D. Michel, Edvige Galeazzi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:2371-2376
The D-1 and D-2 affinities, in vivo femoral and renal vasodilatory effects, oral antihypertensive and diuretic effects and syntheses of selected dopamine congeners are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a12baf334a3eddba10913c6cf19b15d
https://doi.org/10.1016/0960-894x(95)00413-n
https://doi.org/10.1016/0960-894x(95)00413-n
Autor:
Angel Guzman, J. M. Muchowski, M R Van Calsteren, Edvige Galeazzi, J. L. Nava, K. Jankowski, Eduardo Díaz
Publikováno v:
Magnetic Resonance in Chemistry. 33:581-585
The conformation of 1-phenyl-1-(1,2-dimethyl-5-pyrrolyl)-2-(2-methyl-5-benzoyl-1-pyrroly)ethanol, with characteristics of a molecular propeller, is stabilized by intramolecular hydrogen bonding as detected by 1H NMR, NOE difference experiments, 2D NM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39fe499e11718fd6c765a264a1cec347
https://doi.org/10.1002/mrc.1260330715
https://doi.org/10.1002/mrc.1260330715
Autor:
Patricia Saavedra, Joseph M. Muchowski, Denise Yamamoto, Shahin Jamil-Panah, J. M. Young, David J. Morgans, Angel Guzman, Arthur F. Kluge, Francisco Xavier Talamas, Edvige Galeazzi, Philip Teitelbaum, Miguel Salazar
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:1437-1442
Heteroatom substitution within the zileuton nucleus led to a congener series which was evaluated for potency and rate of glucuronidation, a major route for elimination of zileuton. Subtle changes in structure were found to significantly effect glucur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb4db977ebe5f435edb3e085f52272ed
https://doi.org/10.1016/s0960-894x(01)80509-6
https://doi.org/10.1016/s0960-894x(01)80509-6
Autor:
Michael L. Maddox, Angel Guzman, Lilia J. Kurz, Y. Antonio, Robert Greenhouse, Edvige Galeazzi, Joseph M. Muchowski, David A. Lustig, Brian L. Bray, Ma. Elizabeth De La Cruz
Publikováno v:
Canadian Journal of Chemistry. 72:15-22
1-(2-Bromobenzyl)-2-alkanesulfonylpyrroles (1c, 1d) and 1-(4-bromobutyl)-2-methylsulfonfylpyrrols (8) undergo oxidative radical cyclization with partial or complete reductive desulfonylation to the pyrrolizidine derivatives 5 and 9 by an AIBN initiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b6eee81211c3b7dfda05ab44bac2f58
https://doi.org/10.1139/v94-004
https://doi.org/10.1139/v94-004
Autor:
Horn Albert R Van, Tsung T. Li, David Y. Jackson, Edvige Galeazzi, Cooper Gary F, Wren Douglas L, Colin C. Beard
Publikováno v:
The Journal of Organic Chemistry. 58:4280-4286
The four stereoisomeric components of enprostil (1a-d) were prepared using an orthoester Claisen rearrangement of individual propargylic alcohol intermediates 8 to generate the required allene upper chain stereochemistry, followed by one-carbon homol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5d363195558e362248f6b2b5b6a2efd
https://doi.org/10.1021/jo00068a023
https://doi.org/10.1021/jo00068a023
Autor:
G. F. Cooper, Wren Douglas L, A. R. Van Horn, Edvige Galeazzi, Li Tsung-Tee, Colin C. Beard, David Y. Jackson
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::109afcb2ab81795dc26d43bb39ab6dea
https://doi.org/10.1002/chin.199349273
https://doi.org/10.1002/chin.199349273
Autor:
Y. Antonio, Joseph M. Muchowski, Ma. Elizabeth De La Cruz, Robert Greenhouse, Edvige Galeazzi, Angel Guzman, Brian L. Bray, Lilia J. Kurz, David A. Lustig, Michael L. Maddox
Publikováno v:
ChemInform. 25
1-(2-Bromobenzyl)-2-alkanesulfonylpyrroles (1c, 1d) and 1-(4-bromobutyl)-2-methylsulfonfylpyrrols (8) undergo oxidative radical cyclization with partial or complete reductive desulfonylation to the...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56711d0d265492def0f91e2ec1fe9e38
https://doi.org/10.1002/chin.199437037
https://doi.org/10.1002/chin.199437037
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f28b4f5c48e4c10528b02c0a0a00626
https://doi.org/10.1002/chin.199404189
https://doi.org/10.1002/chin.199404189
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac493dd5899f95f5d4b7f1f830a25d83
https://doi.org/10.1002/chin.199532156
https://doi.org/10.1002/chin.199532156
Autor:
Joseph M. Muchowski, A. D. Michel, Richard M. Eglen, L. E. Fisher, R. L. Whiting, Robin D. Clark, D. L. Mcclelland, R. P. Rosenkranz, J. M. Caroon, Edvige Galeazzi
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::947cb29109eceb0a3338249b6b2bd256
https://doi.org/10.1002/chin.199608124
https://doi.org/10.1002/chin.199608124