Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Christophe Menendez"'
Autor:
Despina Palla, Antonia I. Antoniou, Michel Baltas, Christophe Menendez, Philippe Grellier, Elisabeth Mouray, Constantinos M. Athanassopoulos
Publikováno v:
Molecules, Vol 25, Iss 20, p 4858 (2020)
Malaria, despite many efforts, remains among the most problematic infectious diseases worldwide, mainly due to the development of drug resistance by Plasmodium falciparum. The antibiotic fosmidomycin (FSM) is also known for its antimalarial activity
Externí odkaz:
https://doaj.org/article/9b96bbe07c1845878b9466ab49f3f5c5
Autor:
Strahinja Stevanovic, Milan Sencanski, Mathieu Danel, Christophe Menendez, Roumaissa Belguedj, Abdelmalek Bouraiou, Katarina Nikolic, Sandrine Cojean, Philippe M. Loiseau, Sanja Glisic, Michel Baltas, Alfonso T. García-Sosa
Publikováno v:
Molecules, Vol 24, Iss 7, p 1282 (2019)
Due to the lack of approved vaccines against human leishmaniasis and the limitations of the current chemotherapy inducing side effects and drug resistance, development of new, effective chemotherapeutic agents is essential. This study describes the s
Externí odkaz:
https://doaj.org/article/df39e0b494e14ea1ae0280a0c717ab36
Autor:
Christophe Menendez, Despina Palla, Antonia I. Antoniou, Constantinos M. Athanassopoulos, Philippe Grellier, Michel Baltas, Elisabeth Mouray
Publikováno v:
Molecules
Volume 25
Issue 20
Molecules, MDPI, 2020, 25 (20), pp.4858. ⟨10.3390/molecules25204858⟩
Molecules, Vol 25, Iss 4858, p 4858 (2020)
Molecules, 2020, 25 (20), pp.4858. ⟨10.3390/molecules25204858⟩
Volume 25
Issue 20
Molecules, MDPI, 2020, 25 (20), pp.4858. ⟨10.3390/molecules25204858⟩
Molecules, Vol 25, Iss 4858, p 4858 (2020)
Molecules, 2020, 25 (20), pp.4858. ⟨10.3390/molecules25204858⟩
Malaria, despite many efforts, remains among the most problematic infectious diseases worldwide, mainly due to the development of drug resistance by Plasmodium falciparum. The antibiotic fosmidomycin (FSM) is also known for its antimalarial activity
Autor:
Christophe Menendez, Alain Chamayou, Rachel Calvet, Brigitte Guidetti, Michel Baron, Lori Gonnet, Michel Baltas, Christiane André-Barrès
Publikováno v:
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2020, 8 (8), pp.3114-3125. ⟨10.1021/acssuschemeng.9b05886⟩
ACS Sustainable Chemistry & Engineering, 2020, 8 (8), pp.3114-3125. ⟨10.1021/acssuschemeng.9b05886⟩
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2020, 8 (8), pp.3114-3125. ⟨10.1021/acssuschemeng.9b05886⟩
ACS Sustainable Chemistry & Engineering, 2020, 8 (8), pp.3114-3125. ⟨10.1021/acssuschemeng.9b05886⟩
International audience; The mechanochemical synthesis of 1,2,4-triazoles by using a planetary ball-mill is studied starting from hydralazine hydrochloride. Excellent conditions were found for achieving total conversion to intermediate hydrazones in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6df334e6d42e97661b18ca6f863faf3b
https://hal-mines-albi.archives-ouvertes.fr/hal-02519781/document
https://hal-mines-albi.archives-ouvertes.fr/hal-02519781/document
Autor:
Christophe Menendez, Mathilde Maillot, Maria Rosalia Pasca, Giorgia Mori, Beatrice Silvia Orena, Chantal Carayon, Christian Lherbet, Zoia Voitenko, Isabelle Fabing, Michel Baltas
Publikováno v:
French-Ukrainian Journal of Chemistry. 3:82-96
A new series of β-hydroxytriazoles were synthesized and evaluated as Mycobacterium tuberculosis inhibitors. Our strategy implied the synthesis of alkyne precursors through a Barbier reaction between benzaldehydes and propargyl bromide followed by cl
Autor:
Christian Lherbet, Stéphane Balayssac, Robert Martino, Véronique Gilard, Christophe Menendez, Nathalie Martins-Froment, Myriam Malet-Martino, François Couderc
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis
Journal of Pharmaceutical and Biomedical Analysis, Elsevier, 2017, 135, pp.31-49. ⟨10.1016/j.jpba.2016.12.011⟩
Journal of Pharmaceutical and Biomedical Analysis, 2017, 135, pp.31-49. ⟨10.1016/j.jpba.2016.12.011⟩
Journal of Pharmaceutical and Biomedical Analysis, Elsevier, 2017, 135, pp.31-49. ⟨10.1016/j.jpba.2016.12.011⟩
Journal of Pharmaceutical and Biomedical Analysis, 2017, 135, pp.31-49. ⟨10.1016/j.jpba.2016.12.011⟩
The sildenafil analogue adulterant previously identified as a nitroso derivative (nitrosoprodenafil) in a dietary supplement (DS) marketed to increase sexual performance and sold in Europe in the early 2010 s is the same as that found in the same typ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a5da794a38df3731fe39102c479852
https://hal.archives-ouvertes.fr/hal-02060162
https://hal.archives-ouvertes.fr/hal-02060162
Autor:
Christian Lherbet, Zoia Voitenko, Michel Baltas, Christophe Menendez, Chantal Carayon, Tetiana Matviiuk, Nathalie Saffon
Publikováno v:
European Journal of Organic Chemistry. 2014:6538-6546
The tandem reduction/oxidation of fluorenyl compounds was performed with LiAlH4 under air to afford the corresponding 9-hydroxyfluorenyl derivatives in good yields. This methodology with LiAlH4 is unprecedented and most likely proceeds by an organoal
Autor:
Tetiana Matviiuk, Christian Lherbet, Michel Baltas, Andrii I. Kysil, Christophe Menendez, Maria Rosalia Pasca, Frédéric Rodriguez, Beatrice Silvia Orena, Giorgia Mori, Zoia Voitenko, Jan Madacki, Christiane André-Barrès, Sonia Mallet-Ladeira, Jana Korduláková
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2016, 123, pp.462-475. ⟨10.1016/j.ejmech.2016.07.028⟩
European Journal of Medicinal Chemistry, Elsevier, 2016, 123, pp.462-475. ⟨10.1016/j.ejmech.2016.07.028⟩
A series of GEQ analogues bearing pyrrolidinone or pyrrolidine cores were synthesized and evaluated against InhA, essential target for Mycobacterium tuberculosis (M.tb) survival. The compounds were also evaluated against M.tb H37Rv growth. Interestin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6b47aae9b8ed35921cc1afef78d223b
https://hal.archives-ouvertes.fr/hal-02061443
https://hal.archives-ouvertes.fr/hal-02061443
Autor:
Maria Grypioti, Christophe Menendez, Sonia Mallet-Ladeira, Christian Lherbet, Michel Baltas, Swantje Nawratil
Publikováno v:
European Journal of Organic Chemistry. 2014:654-659
Benzyltriazoles have been catalytically oxidized by using CuI and tert-butyl hydroperoxide to yield phenyl(1H-1,2,3-triazol-4-yl)methanone derivatives in good yields at room temperature.
Publikováno v:
Synlett. 23:2623-2626
A novel chlorination reaction on the 5-position of 1,2,3-triazoles, directly from 5H-substituted 1,2,3-triazoles was developed by using copper(II) chloride in pivalic acid. A series of triazoles were thus chlorinated in low to good yields.