Výsledky vyhledávání - "Martin P. Duriska"

Facile dearomatisation of porphyrins using palladium-catalysed hydrazination: the 5,15-diiminoporphodimethenes and their redox products

Autor: Peter Turner, John C. McMurtrie, Martin P. Duriska, Llew Rintoul, Grace L. Simpkins, Oliver B. Locos, Louisa J. Esdaile, Dennis P. Arnold

Publikováno v: Tetrahedron. 70:517-532

The synthesis, electronic absorption and 1H NMR spectra of a suite of novel porphyrinoids derived from meso-bromoporphyrins by palladium-catalysed aminations using ethyl and tert-butylcarbazates are reported. Instead of the expected carbazate-substit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a702821289c5f76c52a9bf41674cfcc7
https://doi.org/10.1016/j.tet.2013.11.006

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meso-Porphyrinylphosphine Oxides: Mono- and Bidentate Ligands for Supramolecular Chemistry and the Crystal Structures of Monomeric {[10,20-Diphenylporphyrinatonickel(II)-5,15-diyl]-bis-[P(O)Ph2] and Polymeric Self-Coordinated {[10,20-Diphenylporphyrinatozinc(II)-5,15-diyl]-bis-[P(O)Ph2]}

Autor: John C. McMurtrie, Dennis P. Arnold, Martin P. Duriska, Peter Turner, Farzad Atefi

Publikováno v: Inorganic Chemistry. 45:6479-6489

A series of porphyrins substituted in one or two meso positions by diphenylphosphine oxide groups has been prepared by the palladium-catalyzed reaction of diphenylphosphine or its oxide with the corresponding bromoporphyrins. Compounds {MDPP−[P(O)P

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::33e553ebeb7deed028cb632f02f65a79
https://doi.org/10.1021/ic060372u

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ChemInform Abstract: Facile Dearomatization of Porphyrins Using Palladium-Catalyzed Hydrazination: The 5,15-Diiminoporphodimethenes (III) and Their Redox Products (IV)

Autor: Louisa J. Esdaile, Oliver B. Locos, Martin P. Duriska, Dennis P. Arnold, Peter Turner, Llew Rintoul, Grace L. Simpkins, John C. McMurtrie

Publikováno v: ChemInform. 45

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b02cf0168092ddf2b0527cb0cc241e02
https://doi.org/10.1002/chin.201425120

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