Zobrazeno 1 - 10 of 22 pro vyhledávání: '"Andrew R. Miksztal"'
1
In Situ Forming Systems (Depots)
Autor: Jeremy C. Wright, Michael Sekar, William W. van Osdol, Su Huey Ching, Andrew R. Miksztal
Publikováno v: Long Acting Injections and Implants ISBN: 9781461405535
In situ forming systems transform into semi-solids (or viscous masses) upon injection and provide sustained release of pharmacological agents, including small molecule drugs, peptides and proteins. These formulations can be utilized for systemic or s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7e4e5b49e51c82207863cca838ef4ee4
https://doi.org/10.1007/978-1-4614-0554-2_9
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2
[Untitled]
Autor: Kwan Leung, Andrew R. Miksztal, Leo Gu, William A. Lee, Nancy Chu, Peter H. Nelson
Publikováno v: Pharmaceutical Research. :161-166
The potential bioavailability improvement of mycophenolic acid (MPA), 1, through ester derivatization was evaluated in monkeys at a dose of 20 mg/kg in this study. The acetyl solketal ester 3 was found to have excellent partition properties but poor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0055f576d7f7442cc055c45186bb9531
https://doi.org/10.1023/a:1015828802490
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3
ChemInform Abstract: Alkene Epoxidations Catalyzed by Iron(III), Manganese(III), and Chromium(III) Porphyrins. Effects of Metal and Porphyrin Substituents on Selectivity and Regiochemistry of Epoxidation
Autor: Teddy G. Traylor, Andrew R. Miksztal
Publikováno v: ChemInform. 21
The products of epoxidation of norbornene, cyclohexene, and adamantylideneadamantane with pentafluoroiodobenzene using as catalysts variously substituted tetraphenylporphyrin complexes of chloroiron (III), chloromanganese(III), and chlorochromium(III
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::de304fb96cce7fb4cdd9aedc0dd892d4
https://doi.org/10.1002/chin.199001084
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5
Partial molal heat capacity of aqueous ferrous chloride from measurements of integral heats of dilution
Autor: Ernest Bernarducci, Lester R. Morss, Andrew R. Miksztal
Publikováno v: Journal of Solution Chemistry. 8:717-727
Heats of dilution of concentrated aqueous solutions (4.43 moles-kg−1) of FeCl2 were measured at 15, 25, and 35°C. The heat capacities of these concentrated solutions were also measured at the same temperatures. From these data the partial molal he
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::86a9228fa7bccae3efedc686ae4ad634
https://doi.org/10.1007/bf00648777
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8
Mechanisms of hemin-catalyzed epoxidations: electron transfer from alkenes
Autor: Teddy G. Traylor, Andrew R. Miksztal
Publikováno v: Journal of the American Chemical Society. 109:2770-2774
L'hexamethyl benzene Dewar se transpose partiellement en hexamethylbenzene au cours de son epoxydation a l'aide de chlorure de (tetraphenylporphyrinato) fer(III) et d'acide chloro-3 perbenzoique. De la meme maniere, l'hexahydro-1,4,4a,5,8,8a dimethan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::10610a10446d07d67e81608e953b3d77
https://doi.org/10.1021/ja00243a033
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9
Alkene epoxidations catalyzed by iron(III), manganese(III), and chromium(III) porphyrins. Effects of metal and porphyrin substituents on selectivity and regiochemistry of epoxidation
Autor: Teddy G. Traylor, Andrew R. Miksztal
Publikováno v: Journal of the American Chemical Society. 111:7443-7448
The products of epoxidation of norbornene, cyclohexene, and adamantylideneadamantane with pentafluoroiodobenzene using as catalysts variously substituted tetraphenylporphyrin complexes of chloroiron (III), chloromanganese(III), and chlorochromium(III
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ed19e7ef15a6c12bda96e80c1ef860d
https://doi.org/10.1021/ja00201a026
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10
Transient formation of N-alkylhemins during hemin-catalyzed epoxidation of norbornene. Evidence concerning the mechanism of epoxidation
Autor: Beth E. Dunlap, Andrew R. Miksztal, Teddy G. Traylor, Taku Nakano
Publikováno v: Journal of the American Chemical Society. 109:3625-3632
During the course of hemin-catalyzed epoxidation of norbornene and other alkenes, the hemin catalyst is converted to N-alkylhemin by addition to the alkene.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f7d43cc6ebf3ba7e685d657be3b961b0
https://doi.org/10.1021/ja00246a019
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