Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Daniel M. Perrine"'
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ded8e184061a56e42fc7c2be40cc003
https://doi.org/10.1002/chin.199203180
https://doi.org/10.1002/chin.199203180
Publikováno v:
ChemInform. 21
Obtention de benzo [1,2-b:3,4-b':5,6-b″]- et -[1,2-b:4,3-b':5,6-b″] trithiophene. Mecanisme de la reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454d46f87e792301a2fb4e31b854b1fd
https://doi.org/10.1002/chin.199005167
https://doi.org/10.1002/chin.199005167
Publikováno v:
Journal of Chemical Education. 77:1479
A one-pot synthesis of (±)-2-(t-butylamino)-3'-chloropropiophenone (bupropion) as its hydrochloride salt (Zyban, Wellbutrin), an important antidepressant drug used in the treatment of nicotine addiction, is described. The procedure, suitable for stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b1a036b0146c14abefb9c9622a7a75a
https://doi.org/10.1021/ed077p1479
https://doi.org/10.1021/ed077p1479
Autor:
Daniel M. Perrine
Publikováno v:
American Journal of Psychiatry. 156:1123-1123
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e58cd6dc6ffffd329f1be010b4e718b
https://doi.org/10.1176/ajp.156.7.1123
https://doi.org/10.1176/ajp.156.7.1123
Publikováno v:
Journal of Chemical Education. 75:1266
A synthesis of the immediate precursor of the widely used antidepressant fluoxetine (Prozac) is described. The procedure is short, safe, and simple enough to serve as a laboratory exercise for undergraduate students in the second semester of introduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a91e031dd6e9d1986f0d58307744693
https://doi.org/10.1021/ed075p1266
https://doi.org/10.1021/ed075p1266
Autor:
Daniel M Perrine
Publikováno v:
The Lancet. 351:1818
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::949e9ac498b3afb2e19b6f229ecc34bc
https://doi.org/10.1016/s0140-6736(05)78787-0
https://doi.org/10.1016/s0140-6736(05)78787-0
Publikováno v:
Journal of Chemical Education. 69:719
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::742984761abe7dae85f512b01c883b22
https://doi.org/10.1021/ed069p719
https://doi.org/10.1021/ed069p719
Publikováno v:
The Journal of Organic Chemistry. 52:2213-2216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d826a97d7f724b9c8d072e4519482966
https://doi.org/10.1021/jo00387a019
https://doi.org/10.1021/jo00387a019
Autor:
Jacques Kagan, Dov Borovsky, Tian P. Wang, Daniel M. Perrine, Rosemarie Seitz, Allison B. Stokes, R. W. Tuveson
Publikováno v:
Chemosphere. 17:1309-1320
The title compound was known to be a powerful acaricide. Its activity is light-dependent, but unlike most other phototoxic molecules, it displays significant selectivity. For example, it is extremely active against first-instar larvae of the mosquito
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ebb1ceb692cebd6e63c2a33d4465ffc
https://doi.org/10.1016/0045-6535(88)90083-5
https://doi.org/10.1016/0045-6535(88)90083-5
Publikováno v:
The Journal of Organic Chemistry. 54:4203-4205
Obtention de benzo [1,2-b:3,4-b':5,6-b″]- et -[1,2-b:4,3-b':5,6-b″] trithiophene. Mecanisme de la reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85c61d1be63761ca0669e7c1d40f3af7
https://doi.org/10.1021/jo00278a039
https://doi.org/10.1021/jo00278a039