Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Tuan Lormier"'
Autor:
Albert Virgili, José Elguero, Marta Fierros, Concepción Foces- Foces, Antonio L. Llamas-Saiz, Jean-Pierre Galy, Tuan Lormier, Gérard Boyer
Publikováno v:
Molecules, Vol 4, Iss 4, Pp 104-121 (1999)
Three derivatives of 9,9'-biacridine, 2,2'-dihydroxy, 2,2'-dimethoxy and 2,2'-diacetoxy have been prepared. The crystal structure of racemic 2,2'-dimethoxy-9,9'-biacridine CHCl3 1:1 complex has been determined and shows an almost perpendicular confor
Externí odkaz:
https://doaj.org/article/2ec73184cef5496f964ab547a5560e10
Autor:
Stéphanie Gaigé, Anne Abysique, Rym Barbouche, Alain Tonetto, Attilio Di Maio, Maxime Robin, Anh-Tuan Lormier, Jean-Denis Troadec
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 18, p 9838 (2024)
Chalcones constitute an important group of natural compounds abundant in fruits and comestible plants. They are a subject of increasing interest because of their biological activities, including anti-diabetic and anti-obesity effects. The simple chal
Externí odkaz:
https://doaj.org/article/9b094d8de1c2454ebad7767effa830d3
Publikováno v:
Current Medicinal Chemistry. 30
Background: NLS-3 or (R, R) enantiomer of phacetoperane (levophacetoperane) is the reverse ester of methylphenidate, a well-documented psychostimulant marketed for the treatment of attention-deficit/hyperactivity disorder (ADHD) since the end of 1950
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e59997c988924bd0c9f81d6c984b74de
https://doi.org/10.2174/0929867330666230120161837
https://doi.org/10.2174/0929867330666230120161837
Publikováno v:
Tetrahedron Letters. 53:6961-6964
A first palladium catalyzed cross-coupling amination with chiral auxiliaries at the two meso positions of diarylporphyrins was reported. We noticed that, the non-metallation of porphyrins and steric hinderance of the chiral auxiliary play an essentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1d6c1721380765eaa7b3831bc4db4f4
https://doi.org/10.1016/j.tetlet.2012.10.041
https://doi.org/10.1016/j.tetlet.2012.10.041
Publikováno v:
Tetrahedron Letters. 52:3175-3178
General access to 5,15-diarylporphyrins in two steps is described. Generalization of this approach to tetra-substituted porphyrins allows the reproducible preparation of compounds, in some cases with high yields for porphyrins, which can be used in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::979976d72aa6806a4623c75a13905cf8
https://doi.org/10.1016/j.tetlet.2011.04.028
https://doi.org/10.1016/j.tetlet.2011.04.028
Publikováno v:
Il Farmaco. 59:981-986
The study of the relative binding affinity (RBA) to the human alpha and beta estrogen receptors (ERs) of various 7-hydroxycoumarins substituted at 4- and 3,4- positions is weak and lacks in selectivity for both ERalpha and ERbeta. The 4-(4-hydroxyphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f3259d98cfa6b521e601731dcfa9524
https://doi.org/10.1016/j.farmac.2004.08.004
https://doi.org/10.1016/j.farmac.2004.08.004
Autor:
Anh Tuan Lormier, Sandrine Cojean, Philippe M. Loiseau, Zahra Abada, Bruno Figadère, Bernardin Akagah, Laurent Ferrié, Sébastien Pomel
Publikováno v:
European journal of medicinal chemistry. 67
Importance of heme in African trypanosomes, Leishmania sp. and Plasmodium sp. metabolisms justifies considering the potential of porphyrins and their precursors and derivatives as potential antiparasitic agents by interfering with heme metabolism. Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee0ffe20a1619b137cee514ed1187ae6
https://pubmed.ncbi.nlm.nih.gov/23851117
https://pubmed.ncbi.nlm.nih.gov/23851117
Publikováno v:
The Journal of organic chemistry. 72(7)
Electron-poor 6-oxo-1-sulfonyl-1,6-dihydropyridine-3-carboxylates 1b−d undergo cross-Diels−Alder reactions with electron-rich dienes 4a−f under hyperbaric conditions, reacting either as dienophiles to yield normal-electron-demand (NED) cycloadd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb5692cc87dce8a38977a30f9f08d28
https://pubmed.ncbi.nlm.nih.gov/17346084
https://pubmed.ncbi.nlm.nih.gov/17346084
Publikováno v:
ChemInform. 36
The study of the relative binding affinity (RBA) to the human α and β estrogen receptors (ERs) of various 7-hydroxycoumarins substituted at 4- and 3,4- positions is weak and lacks in selectivity for both ERα and ERβ. The 4-(4-hydroxyphenyl)-7-hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc109a0f54580f7e4437590b03469675
https://doi.org/10.1002/chin.200516124
https://doi.org/10.1002/chin.200516124
Publikováno v:
Tetrahedron Letters. 54:1900
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62398cb2d4a9e2b0e697bbcf8fbb0d9e
https://doi.org/10.1016/j.tetlet.2013.02.010
https://doi.org/10.1016/j.tetlet.2013.02.010