Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Michel Momenteau"'
Autor:
Michel Momenteau
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 100:731-742
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9033209e4f23bf56a0067d6cb00442b5
https://doi.org/10.1002/bscb.19911001003
https://doi.org/10.1002/bscb.19911001003
Autor:
D. Oulmi, Erika Balog, Ph. Maillard, István Voszka, Gabriella Csík, F. Tölgyesi, Michel Momenteau
Publikováno v:
Journal of Photochemistry and Photobiology B: Biology. 44:216-224
A series of glucose- or galactose-residue-bearing tetraphenyl porphyrins (TPPs) has recently been synthesized with the aim of studying the structural dependence of porphyrin cellular localization and efficiency in photodynamic therapy (PDT). For the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81317d6a030257f709895a53550fe3d8
https://doi.org/10.1016/s1011-1344(98)00147-x
https://doi.org/10.1016/s1011-1344(98)00147-x
Autor:
Anastasios Troganis, Michel Momenteau, Charalampos G. Kalodimos, Ioannis P. Gerothanassis, Bernard Loock
Publikováno v:
Journal of Biomolecular NMR. 11:423-435
13C NMR spectra of several carbon monoxide (99.7% 13C and 11.8% 18O enriched) hemoprotein models with varying polar and steric effects of the distal organic superstructure and constraints of the proximal side are reported. This enables the 57Fe-13C(O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ae5fe40fbc3ca274e0626a56cc50f3e
https://doi.org/10.1023/a:1008253901009
https://doi.org/10.1023/a:1008253901009
Publikováno v:
Tetrahedron Letters. 38:3731-3734
Amphiphilic glycoconjugated benzochlorin was prepared efficiently from meso monoaryl porphyrin and 3-(dimethylamino)acrolein by regiospecific Vilsmeier's reaction followed by cyclisation under acidic conditions and glycosylation. This compound displa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98bb115a45b21c75109959e46584fb46
https://doi.org/10.1016/s0040-4039(97)00711-9
https://doi.org/10.1016/s0040-4039(97)00711-9
Publikováno v:
Journal of the American Chemical Society. 119:3536-3542
The reduction of rhodium(III) porphyrins in polar aprotic solvents is a two-electron irreversible reaction yielding directly the Rh(I) complex. The cause of this irreversibility is not the metal−metal dimerization of the initially formed Rh(II) com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::898d7c6872f66fd79094b2a3e45b46d8
https://doi.org/10.1021/ja964023i
https://doi.org/10.1021/ja964023i
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 113:23-34
New chiral porphyrins bearing glycosyl substituents (glucose, maltose or lactose) at ortho or meta positions of the meso-phenyl groups have been synthesized. Their manganese complexes, associated with hydrogen monopersulfate, lithium hypochlorite, hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb023074995a3a670ec9bf0307053d8d
https://doi.org/10.1016/s1381-1169(96)00038-6
https://doi.org/10.1016/s1381-1169(96)00038-6
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 113:201-208
Three new chiral managanese(III) porphyrins bearing chloro and glucosyl substituents have been used as catalysts for enantiomeric epoxidation of 4-chlorostyrene in the presence of diluted hydrogen peroxide as oxygen donor. With such complexes enantio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea3400c9e33f0111f680263d7ed9be7e
https://doi.org/10.1016/s1381-1169(96)00056-8
https://doi.org/10.1016/s1381-1169(96)00056-8
Autor:
Michel Momenteau, Hermas R. Jiménez
Publikováno v:
Inorganica Chimica Acta. 244:171-177
The synthesis and characterization of rhodium ‘two-face’ hindered porphyrins are reported. Three new metalloporphyrins were obtained from the metallation of ‘basket-handle’ porphyrins in dimethylformamide. The synthesized compounds are repres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbd5c11367265c2d61c6ffdbaa9305c8
https://doi.org/10.1016/0020-1693(95)04774-3
https://doi.org/10.1016/0020-1693(95)04774-3
Autor:
Arezki Boudif, Michel Momenteau
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :1235-1242
A new methodology based on the ‘3 + 1’ acid-catalytic condensation of tripyrranes and pyrrole-2,5-dicarbaldehyde has been used, for the first time, for the synthesis of two types of porphyrins: vic-dipropionic ester porphyrins 30 and 31 including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a738b1d6dee6d28fb86764eecd91f9a3
https://doi.org/10.1039/p19960001235
https://doi.org/10.1039/p19960001235
Publikováno v:
Journal of the American Chemical Society. 117:6041-6047
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c78aafcd94166b70a14b0f2fc5b7e89b
https://doi.org/10.1021/ja00127a017
https://doi.org/10.1021/ja00127a017