Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maryvonne Le Plouzennec"'
Autor:
Maryvonne Le Plouzennec, Annie Bourseul, Géraldine Poignant, Paul Le Maux, Thierry Patrice, Claude Moinet, Arnaud Bondon, Véronique Vonarx, Catherine Gèze, Gérard Simonneaux
Publikováno v:
Tetrahedron Letters. 37:7511-7514
The synthesis and NMR characterization of chiral mesoporphyrins bearing α-methoxy-α-(trifluoromethyl) phenylacetyl residues are reported. The phototoxicity with circular polarized light and intracellular localization in L1210 cells are also describ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df98d1f90944dfd44d3f601bd4754a79
https://doi.org/10.1016/0040-4039(96)01726-1
https://doi.org/10.1016/0040-4039(96)01726-1
Autor:
Marie Thérèse Foultier, Gérard Simonneaux, Francois Hindré, Jacques D. de Certaines, Maryvonne Le Plouzennec, Thierry Patrice
Publikováno v:
Journal of Magnetic Resonance Imaging. 3:59-65
Tetra-P-aminophenylporphyrin (TPP) was conjugated with gadolinium diethylenetriaminepen-taacetic acid (DTPA) and used as a contrast agent in magnetic resonance (MR) imaging to achieve tumor selectivity in nude mice. A substantial decrease in T1 was m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6880762abe1b2ab32173ac85c8b8c561
https://doi.org/10.1002/jmri.1880030111
https://doi.org/10.1002/jmri.1880030111
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1169
Azobenzene-substituted prophyrins have been synthesised by condensation of aminophenylporphyrins and nitrosophenyl derivatives; intramolecular fluorescence quenching is detected in the ortho position.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31831f43c4d8439821797422d6938854
https://doi.org/10.1039/c39940001169
https://doi.org/10.1039/c39940001169
Publikováno v:
Inorganic Chemistry. 25:1254-1257
Preparation des complexes cites dans le titre et leur etude par diverses methodes spectroscopiques. Ce travail montre une analogie frappante entre les proprietes liantes des N-acylisocyanure et le monoxyde de carbone comme coordinat des porphyrines f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::997b0229c9a207178e0d351bd37112a7
https://doi.org/10.1021/ic00228a036
https://doi.org/10.1021/ic00228a036
Publikováno v:
Journal of Organometallic Chemistry. 122:365-376
The photochemical substitution, by various phosphines or phosphites, of the carbonyl ligands of derivatives of cymantrene has been studied, giving evidence of the effect of the electron density on the metal for mono- or di-substitution. Optically act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd016e8d1d16d5c97c74704046aed2e8
https://doi.org/10.1016/s0022-328x(00)82398-0
https://doi.org/10.1016/s0022-328x(00)82398-0
Publikováno v:
Journal of Organometallic Chemistry. 111:C38-C42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cc011318ac12fb6189a9af973844519
https://doi.org/10.1016/s0022-328x(00)98148-8
https://doi.org/10.1016/s0022-328x(00)98148-8
Autor:
Rene Dabard, Maryvonne Le Plouzennec
Publikováno v:
Journal of Organometallic Chemistry. 133:359-375
Summary The absolute configuration of β-(2-methyl- or 3-methyl-cymantrenoyl) α,α-dimethylpropionic acids is ascertained by chemical correlation with (−) 2-methylcymantrenoic acid. The determination of the absolute configuration of related compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd4d48704e8219a8af7aaed0d128185e
https://doi.org/10.1016/s0022-328x(00)89136-6
https://doi.org/10.1016/s0022-328x(00)89136-6
Publikováno v:
Journal of Organometallic Chemistry. 132:409-418
Various studies by p K a measurements, v (CO) frequencies and NMR data on the photochemical replacement of CO by various phosphines or phosphites provide information on the metal—ligand bond strength in the derivatives of cymantrene. For pseudo-tet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be7f69364c31881b53d61b14cc310bce
https://doi.org/10.1016/s0022-328x(00)93726-4
https://doi.org/10.1016/s0022-328x(00)93726-4
Autor:
Rene Dabard, Maryvonne Le Plouzennec
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99ceddae04e77cf5a22c062eb089cead
https://doi.org/10.1002/chin.197251408
https://doi.org/10.1002/chin.197251408
Autor:
Rene Dabard, Maryvonne Le Plouzennec
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8664110cc80f9c40c063b5dca4303f7
https://doi.org/10.1002/chin.197251409
https://doi.org/10.1002/chin.197251409