Zobrazeno 1 - 9 of 9 pro vyhledávání: '"DAVID M. MARYNIAK"'
1
Uncoupling Oxygen Transfer and Electron Transfer in the Oxygenation of Camphor Analogues by Cytochrome P450-CAM
Autor: David M. Maryniak, John H. Dawson, Eric D. Coulter, Thomas A. Bryson, Saloumeh Kadkhodayan
Publikováno v: Journal of Biological Chemistry. 270:28042-28048
The hydroxylation of (1R)-camphor by cytochrome P450-CAM involves almost complete coupling of electron to oxygen transfer. Modifications at C-5 of camphor, the normal site of hydroxylation by P450-CAM, lead to as much as 98% uncoupling of electron an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8313548077cd0edb14c36279c0abb9d8
https://doi.org/10.1074/jbc.270.47.28042
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2
The syntheses of 1R- and 1S-5-methylenylcamphor and their epoxidation by cytochrome P-450-CAM
Autor: John H. Dawson, George B. Crull, Thomas A. Bryson, David M. Maryniak, Saloumeh Kadkhodayan
Publikováno v: Tetrahedron. 49:9373-9384
The syntheses of 1R- and 1S-5-methylenylcamphor, camphor analogues in which the two methylene hydrogens at C-5 have been replaced with an exocyclic methylene group, are described. The stereospecific epoxidations of both olefins by Pseudomonas putida
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fb4b3d263157025f942c94cdec30abb0
https://doi.org/10.1016/0040-4020(93)80022-l
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3
ChemInform Abstract: The Syntheses of (1R)- and (1S)-5-Methylenylcamphor and Their Epoxidation by Cytochrome P-450-CAM
Autor: John H. Dawson, Thomas A. Bryson, Saloumeh Kadkhodayan, David M. Maryniak, George B. Crull
Publikováno v: ChemInform. 25
The syntheses of 1R- and 1S-5-methylenylcamphor, camphor analogues in which the two methylene hydrogens at C-5 have been replaced with an exocyclic methylene group, are described. The stereospecific epoxidations of both olefins by Pseudomonas putida
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e777f3e54c420a9536bc343ce2cd8ea1
https://doi.org/10.1002/chin.199404224
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4
ChemInform Abstract: Studies on Antifungal Agents. In vitro Activity of Novel cis-5-Alkoxy-(or Acyloxy)alkyl-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidine Derivatives
Autor: S. D. Allen, J. T. Mitchell, V. St. Georgiev, David M. Maryniak, George B. Mullen, C. R. Kinsolving
Publikováno v: ChemInform. 21
The synthesis and in vitro antifungal activity of a novel series of cis-5-alkoxy(or acyloxy)alkyl-3-phenyl-3-(1H-imidazol-1-ylmethyl)- 2-methylisoxazolidine derivatives (6a-n) are described. The 5-[(4-chlorobenzyloxy)methyl] analogue 6h and the two 5
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1e8391a01f6e741c1b9b27402114bbbc
https://doi.org/10.1002/chin.199023316
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5
Substituted 5-Phenoxyalkyl-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines
Autor: GEORGE B. MULLEN, DAVID M. MARYNIAK, PATRICIA A. SWIFT, STANLEY D. ALLEN, JEFFREY T. MITCHELL, C. RICHARD KINSOLVING, VASSIL ST. GEORGIEV
Publikováno v: Annals of the New York Academy of Sciences. 544:359-362
Substituted 5-(phenoxyalkyl)-3-phenyl-3-(1H-imidazol-1-ylmethyl)-2-methylisoxazolidines, in which hydrogens of their benzene rings may be replaced by halogen, lower alkoxy, lower alkyl, nitro, acetamido and/or trifluoromethyl groups, are useful as an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ce3043e30ae6fb16ce7040f114a87e
https://doi.org/10.1111/j.1749-6632.1988.tb40422.x
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