Zobrazeno 1 - 10
of 10
pro vyhledávání: '"John F. Arnett"'
Autor:
Mark D. Lauritsen, Goss S. Kauffman, Kimberly A. Nelson, Walter M. Bryant, Richard E. Olson, Gary O. Page, Lisa M. Lloyd, James Segretario, George F. Huhn, John F. Arnett, Pesti Jaan A, Christopher S. Bamum, Edward F. Gorko, Jill A. Downard, Robert E. Yule, Joseph J. Mrowca
Publikováno v:
Journal of Heterocyclic Chemistry. 35:249-255
The methanesulfonates of (α-(4-chlorophenyl)-α-[1-(2-chlorophenyl)ethenyl]-1H-1,2,4-triazole-1-ethanol and α-[1-(2-chlorophenyl)ethenyl]-α-(2,4-difluorophenyl)-1H-1,2,4-triazole-1-ethanol (1a, b) are orally effective α-styryl carbinol derivative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4e11eec83289b50d611174679ccae58
https://doi.org/10.1002/jhet.5570350144
https://doi.org/10.1002/jhet.5570350144
Autor:
James R. Moore, Robert A. Reamer, Chen Cheng Y, Sidney Brookes, Bruce S. Foster, Edward G. Corley, Anthony O. King, David M. Tschaen, Lucius Thomas Rossano, F. Edward Roberts, Thomas R. Verhoeven, John F. Arnett, David R. Lieberman, Paul J. Reider, Chunhua Yang, Robert D. Larsen, Meloni David J, S. Lo Young
Publikováno v:
The Journal of Organic Chemistry. 59:6391-6394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2613c46ff25d0baa37fd84c6c2af2d0
https://doi.org/10.1021/jo00100a048
https://doi.org/10.1021/jo00100a048
Publikováno v:
The Journal of Organic Chemistry. 58:4642-4645
DuP 532 (2), which is a potent angiotensin II receptor antagonist, has been prepared by two different routes. One route, which is more practical for large-scale synthesis, required the preparation of methyl 4(5)-(pentafluoroethyl)-2-propylimidazole-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1d1d4268cd709410a483885ffa73b51
https://doi.org/10.1021/jo00069a029
https://doi.org/10.1021/jo00069a029
Publikováno v:
ChemInform. 24
DuP 532 (2), which is a potent angiotensin II receptor antagonist, has been prepared by two different routes. One route, which is more practical for large-scale synthesis, required the preparation of methyl 4(5)-(pentafluoroethyl)-2-propylimidazole-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffab6b066693bcb4d9c2015415df3515
https://doi.org/10.1002/chin.199351154
https://doi.org/10.1002/chin.199351154
Autor:
Meloni David J, Ying-Chi Lee, John F. Arnett, James R. Moore, Lucius Thomas Rossano, Young S. Lo
Publikováno v:
Journal of Heterocyclic Chemistry. 32:355-357
Understanding the mechanism of formation of an impurity in the key step of the synthesis of Losartan (1) helped devise a procedure to synthesize the title compound in high yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23d10aad10bcf81242c66a89af30c8ed
https://doi.org/10.1002/jhet.5570320160
https://doi.org/10.1002/jhet.5570320160
Autor:
John F. Arnett, H. M. Walborsky
Publikováno v:
The Journal of Organic Chemistry. 37:3678-3683
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2d839d335f3024d6d7af3157382b8de
https://doi.org/10.1021/jo00796a024
https://doi.org/10.1021/jo00796a024
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fdfa4129d0addf31ca8ad3eaaff8163
https://doi.org/10.1002/chin.197514418
https://doi.org/10.1002/chin.197514418
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff5a4339762c87af43a6758c6f2b90ee
https://doi.org/10.1002/chin.197431063
https://doi.org/10.1002/chin.197431063
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2ea010ec4a4043589f1d3f708af3e26
https://doi.org/10.1002/chin.197351079
https://doi.org/10.1002/chin.197351079
Publikováno v:
Journal of the American Chemical Society. 97:430-431
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d18609c5ec74fcb1a33526942a7cd708
https://doi.org/10.1021/ja00835a039
https://doi.org/10.1021/ja00835a039