Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Beth E. Dunlap"'
Publikováno v:
ChemInform. 23
Hydroxylation of aliphatic hydrocarbons with oxidants such as iodosobenzene can be effectively catalyzed with highly halogenated iron(III) porphyrins such as iron(III) tetrakis(2,6-dichlorophenyl)octabromoporphyrin. Hydroxylation of norbornane and te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea37a07bab87237a5251ea3666b77c89
https://doi.org/10.1002/chin.199222103
https://doi.org/10.1002/chin.199222103
Publikováno v:
Journal of the American Chemical Society. 114:1308-1312
Hydroxylation of aliphatic hydrocarbons with oxidants such as iodosobenzene can be effectively catalyzed with highly halogenated iron(III) porphyrins such as iron(III) tetrakis(2,6-dichlorophenyl)octabromoporphyrin. Hydroxylation of norbornane and te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e842e922933695915fae64333d7548be
https://doi.org/10.1021/ja00030a028
https://doi.org/10.1021/ja00030a028
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
https://doi.org/10.1021/ja00246a019
Publikováno v:
Journal of the American Chemical Society. 108:2782-2784
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c8a32d50a8652e7f3c087ccf0edee43
https://doi.org/10.1021/ja00270a063
https://doi.org/10.1021/ja00270a063
Publikováno v:
Journal of the American Chemical Society. 107:5537-5539
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1673590c65698cf03268dfbf78f9af6
https://doi.org/10.1021/ja00305a042
https://doi.org/10.1021/ja00305a042
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03b71b928de81306e55d8333677a02c9
https://doi.org/10.1002/chin.198637270
https://doi.org/10.1002/chin.198637270
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a67b31357425e390c65ddf88834ba90
https://doi.org/10.1002/chin.198601102
https://doi.org/10.1002/chin.198601102
Publikováno v:
Oxygen Radicals in Biology and Medicine ISBN: 9781468455700
Iron(III) porphyrins efficiently catalyze the epoxidation of alkenes and the hydroxylation of alkanes by iodosylbenzenes and peracids, most likely by the same mechanisms utilized by cytochrome P-450 enzymes. The synthetic catalysts mimic the enzymes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a20ad8755e31fedd64e61a2403992cb
https://doi.org/10.1007/978-1-4684-5568-7_78
https://doi.org/10.1007/978-1-4684-5568-7_78
Publikováno v:
ChemInform. 18
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_________::8bc934bdc7b097769141f19df581353b
https://doi.org/10.1002/chin.198741370
https://doi.org/10.1002/chin.198741370
Autor:
Debkumar Bandyopadhyay, Paul Maffuid, Wen-Pang Fann, Feng Xu, Beth E. Dunlap, Joseph P. Ciccone, Teddy G. Traylor, Shinji Tsuchiya
Publikováno v:
Journal of Inorganic Biochemistry. 36:313
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a27ab171c25c4a96100c7f4db1536c5e
https://doi.org/10.1016/0162-0134(89)84486-1
https://doi.org/10.1016/0162-0134(89)84486-1