Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dorothée Razafimahefa"'
Autor:
Amélie Lemoine, Bakolinirina Andriamihaja, F. Bailleul, Sevser Sahpaz, Heritiana Ranarivelo, Nathalie Duhal, Dorothée Razafimahefa, Sania Mahamodo, Amin Abedini, Céline Rivière, Vincent Roumy, Christel Neut, Thierry Hennebelle, Bakonirina Razanamahefa
Publikováno v:
Phytochemistry. 102:162-168
Bioassay-guided fractionation using antimicrobial assay of the crude acetonic extract of Garcinia goudotiana leaves and of its five partitions led to the isolation of two new prenylated benzoylphloroglucinol derivatives, goudotianone 1 ( 1 ) and goud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f5c3e21727f69abc9760a9487e1e015
https://doi.org/10.1016/j.phytochem.2014.03.006
https://doi.org/10.1016/j.phytochem.2014.03.006
Autor:
David Ramanitrahasimbola, François Frappier, Dorothée Razafimahefa, Marie-Thérèse Martin, Lengo Mambu, Philippe Rasoanaivo
Publikováno v:
Planta Medica
Planta Medica, Georg Thieme Verlag, 2000, 66, pp.537-540
Planta Medica, Georg Thieme Verlag, 2000, 66, pp.537-540
From stem barks of Isolona guesquiereina three known bisbenzylisoquinolines were isolated and identified as (-)-curine, chondrofoline and isochondodendrine. Structures were established mainly on the basis of comparison of their physical and spectral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0c5b2be601d5933dffd8d32c3b4842a
https://doi.org/10.1055/s-2000-8610
https://doi.org/10.1055/s-2000-8610
Autor:
Jeanne Maugein, Sylvia Lauvagie, Lies Hammouche, Christiane Bebear, Dorothée Razafimahefa, Lydie Pelinski, Jacques Brocard, Dimby Andrianina Ralambomanana
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2005, 15, pp.2301-2303. ⟨10.1016/j.bmcl.2005.03.004⟩
Bioorganic and Medicinal Chemistry Letters, 2005, 15, pp.2301-2303. ⟨10.1016/j.bmcl.2005.03.004⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2005, 15, pp.2301-2303. ⟨10.1016/j.bmcl.2005.03.004⟩
Bioorganic and Medicinal Chemistry Letters, 2005, 15, pp.2301-2303. ⟨10.1016/j.bmcl.2005.03.004⟩
International audience; A new series of ferrocenyl diamino alcohols and diamines were synthesized and their inhibitory potencies were probed with Mycobacterium tuberculosis. Interestingly, ferrocenyl diamines display significant activities against M.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e781978005617180a5636e6727c7134
https://doi.org/10.1016/j.bmcl.2005.03.004
https://doi.org/10.1016/j.bmcl.2005.03.004
Autor:
Dorothée Razafimahefa-Ramilison, Jeanne Maugein, Lydie Pelinski, Dimby Andrianina Ralambomanana, Andry Clément Rakotohova
Publikováno v:
Bioorganicmedicinal chemistry. 16(21)
A total of 21 ferrocenyl and benzyl diaminoalcohols and diamines were synthesized and evaluated against Mycobacterium tuberculosis H37Rv. Interestingly, ferrocenyl diamines exhibit better activities than ferrocenyl diaminoalcohols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfc073c2f0b5eacde9e434e9fa58ede8
https://pubmed.ncbi.nlm.nih.gov/18835177
https://pubmed.ncbi.nlm.nih.gov/18835177
Autor:
Jacques Brocard, Dorothée Razafimahefa, David Ramanitrahasimbola, Marie-Thérèse Martin, Lydie Pelinski, Philippe Rasoanaivo
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2005, 15, pp.1239-1241. ⟨10.1016/j.bmcl.2004.11.067⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2005, 15, pp.1239-1241. ⟨10.1016/j.bmcl.2004.11.067⟩
Bioorganic and Medicinal Chemistry Letters, 2005, 15, pp.1239-1241. ⟨10.1016/j.bmcl.2004.11.067⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2005, 15, pp.1239-1241. ⟨10.1016/j.bmcl.2004.11.067⟩
International audience; Several strychnobrasiline derivatives have been synthesized to overcome the lack of in vivo reversal activity of the parent compound. In the present study, Na-deacetyl-ferrocenoyl-strychnobrasiline was synthesized by condensin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0286137521910a05bcd50f7e49b38676
https://hal.science/hal-00115540
https://hal.science/hal-00115540
Publikováno v:
Tetrahedron: Asymmetry
Tetrahedron: Asymmetry, Elsevier, 2005, 16, pp.1189. ⟨10.1016/j.tetasy.2005.01.041⟩
Tetrahedron: Asymmetry, 2005, 16, pp.1189. ⟨10.1016/j.tetasy.2005.01.041⟩
Tetrahedron: Asymmetry, Elsevier, 2005, 16, pp.1189. ⟨10.1016/j.tetasy.2005.01.041⟩
Tetrahedron: Asymmetry, 2005, 16, pp.1189. ⟨10.1016/j.tetasy.2005.01.041⟩
8 pages; International audience; A series of enantiopure 1,4-amino alcohols with a [3]ferrocenophane backbone have been synthesized. Candida rugosa lipases were used in a key step allowing the resolution of amino alcohol (1S,Rp)-1. Two other amino al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16901390dd656e03ee1809a02d69cc24
https://hal.archives-ouvertes.fr/hal-00100251
https://hal.archives-ouvertes.fr/hal-00100251