Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Alain Kossanyi"'
Autor:
Catherine Verchère-Béaur, Samia Far, Nohad Gresh, Alain Kossanyi, Martine Perrée-Fauvet, Eliane Taillandier
Publikováno v:
European Journal of Organic Chemistry. 2004:1781-1797
In order to increase the DNA binding affinity of a bis-arginyl-porphyrin which has been previously shown to bind preferentially in the major groove of the d(GGCGCC)2 sequence (Mohammadi et al., Biochemistry1998, 37, 9165), we have synthesized bis- an
Publikováno v:
Chemistry - A European Journal. 7:2862-2872
Hydrogen-bond formation with the terminal oxygen atom is considered to be the basis of dioxygen molecule activation by cytochrome P450. In order to verify the effect of this hydrogen bond, we have undertaken the synthesis of a model complex: a binaph
Publikováno v:
Synthetic Communications. 29:4341-4346
The synthesis of 9-acridinecarboxamide derivatives has been improved through the choice of better reaction conditions and the devising of an original treatment step. Extended amino chains are thus easily and reliably coupled to the commercially avail
Publikováno v:
ChemInform. 31
The synthesis of 9-acridinecarboxamide derivatives has been improved through the choice of better reaction conditions and the devising of an original treatment step. Extended amino chains are thus easily and reliably coupled to the commercially avail
Publikováno v:
Coordination Chemistry Reviews
Coordination Chemistry Reviews, Elsevier, 1998, 178-180, pp.1407-1431
Coordination Chemistry Reviews, 1998, 178-180, pp.1407-1431. ⟨10.1016/S0010-8545(98)00148-9⟩
Coordination Chemistry Reviews, Elsevier, 1998, 178-180, pp.1407-1431. ⟨10.1016/S0010-8545(98)00148-9⟩
Coordination Chemistry Reviews, Elsevier, 1998, 178-180, pp.1407-1431
Coordination Chemistry Reviews, 1998, 178-180, pp.1407-1431. ⟨10.1016/S0010-8545(98)00148-9⟩
Coordination Chemistry Reviews, Elsevier, 1998, 178-180, pp.1407-1431. ⟨10.1016/S0010-8545(98)00148-9⟩
Three kinds of biomimetic heme precursors have been prepared. The first type is based on tetra-aminoporphyrins: either 5,10,15,20-tetrakis (o-aminophenyl)porphyrin (various atropoisomers), or 5,15-bis(2′,6′-diaminophenyl)porphyrin. The second typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::070fbd48d7ee9d1064f9dcebdc4972d8
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01469616
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01469616
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 1993, 34 (45), pp.7267-7270
Tetrahedron Letters, 1993, 34 (45), pp.7267-7270
Tetrahedron Letters, Elsevier, 1993, 34 (45), pp.7267-7270
Tetrahedron Letters, 1993, 34 (45), pp.7267-7270
UV-Vis studies of two heme protein models differing only by two carbons show unexpected oxygen and carbonmonoxide affinities and in one case a partition coefficient M = 105 which can be compared favorably with hemoprotein values.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdbe9d0825a576c537d954c7e225ab86
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01469811
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01469811
Autor:
Bernard Desmazieres, Mélanie Quelquejeu, Aurelien Cardon-Pilotaz, Alain Kossanyi, Eric Rose, Nicolas Bernard
Publikováno v:
The Journal of Organic Chemistry. 60:3919-3920
Publikováno v:
The Journal of Organic Chemistry. 58:5030-5031
A 72% abundance of α,βα,β-atropoisomer was observed in the thermal treatment of 4 g of meso-5,10,-15,20-tetrakis(o-nitrophenyl)porphyrin in 800 g of naphthalene at 130 o C. The rt reduction of the nitro groups with SnCl 2 and HCl followed by chro
Autor:
Samia Far, Alain Kossanyi, Catherine Verchère-Béaur, Nohad Gresh, Eliane Taillandier, Martine Perrée-Fauvet
Publikováno v:
European Journal of Organic Chemistry; Apr2004, Vol. 2004 Issue 8, p1781-1797, 17p