Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Clémence Tabélé"'
Publikováno v:
Molecules, Vol 20, Iss 12, Pp 22890-22899 (2015)
Cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids are used to obtain aromatic-(2-methylallyl) derivatives. However, deboronation or isomerization side reactions may occur for several boronic acids. We describe herein t
Externí odkaz:
https://doaj.org/article/7cc921336e744a86898d2b2e3afaaa14
Autor:
Clémence Tabélé, marc montana, christophe curti, thierry terme, pascal rathelot, sophie gensollen, patrice vanelle
Publikováno v:
Journal of Pharmacy & Pharmaceutical Sciences, Vol 15, Iss 1 (2012)
Since 1976, fibrin glues have been attracting medical interest, spreading from their initial use as a hemostatic agent in cardiovascular surgery to other fields of surgery. Studies have compared the efficacy of fibrin glues vs sutures in surgery. How
Externí odkaz:
https://doaj.org/article/aa6c509c6372441ca8ac54a349088892
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Patrice Vanelle, Viviane dos Santos Faiões, Omar Khoumeri, Fabien Grimaud, Eduardo Caio Torres-Santos, Clémence Tabélé, Christophe Curti
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2018, 148, pp.154--164. ⟨10.1016/j.ejmech.2018.02.029⟩
European Journal of Medicinal Chemistry, 2018, 148, pp.154--164. ⟨10.1016/j.ejmech.2018.02.029⟩
European Journal of Medicinal Chemistry, Elsevier, 2018, 148, pp.154--164. ⟨10.1016/j.ejmech.2018.02.029⟩
European Journal of Medicinal Chemistry, 2018, 148, pp.154--164. ⟨10.1016/j.ejmech.2018.02.029⟩
WOS:000428824700013; In continuation to our previous findings on amidoximes' antiparasitic activities, a new series of 23 original derivatives was designed and obtained by convergent synthesis. First, new terminal alkenes were synthesized by cross-co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de38ddf3888ac96a33823055bcbcdbba
https://doi.org/10.1016/j.ejmech.2018.02.029
https://doi.org/10.1016/j.ejmech.2018.02.029
Autor:
Ngoc Anh Thu Nguyen, Pascal Auquier, Any Beltran Anzola, Roseline D’oiron, Thierry Lambert, Céline Falaise, Christine Biron, Anne Lienhart, Jenny Goudemand, Antoine Rauch, Bénédicte Wibaut, Sabine Marie Castet, Dominique Desprez, Annie Harroche, Natalie Stieltjes, Annie Borel-Derlon, Marc Trossaërt, Amandine Celli, Benoît Guillet, Sophie Bayart, Marie-Anne Bertrand, Alexandra Fournel, Guillaume Mourey, Valérie Gay, Pierre Chamouni, Emmanuelle DE Raucourt, Birgit Frotscher, Michèle Martin, Mathieu Puyade, Brigitte Tardy, Stéphane Vanderbecken, Fabienne Genre-Volot, Philippe Nguyen, Benoît Polack, Caroline Oudot-Challard, Stéphane Girault, Annelise Voyer, Aurélien Lebreton, Abel Hassoun, Philippe Moreau, Pierre-Simon Rohrlich, Karine Baumstarck, Mohamed Boucekine, Vanessa Milien, Natacha Rosso, Clemence Tabele, Marie Viprey, Nicolas Giraud, Thomas Sannie, Hervé Chambost, Noémie Resseguier
Publikováno v:
HemaSphere, Vol 7, p e623777c (2023)
Externí odkaz:
https://doaj.org/article/35f0ccb00974432f92e9847dd92e5503
Autor:
Vincent Remusat, Patrice Vanelle, Nicolas Primas, Youssef Kabri, Christophe Curti, Clémence Tabélé
Publikováno v:
ChemInform. 47
To obtain aromatic 2-methylallyl derivatives, cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids were studied. Among allylic alcohols described for such cross-coupling reactions, 2-methyl-2-propen-1-ol has a low reactiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b2afc2e79f9bb050f2765fd51099be9
https://doi.org/10.1002/chin.201610067
https://doi.org/10.1002/chin.201610067
Publikováno v:
Molecules; Volume 20; Issue 12; Pages: 22890-22899
Cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids are used to obtain aromatic-(2-methylallyl) derivatives. However, deboronation or isomerization side reactions may occur for several boronic acids. We describe herein t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::a8980c0f855f530d7c17e5a207234f29
Autor:
Nicolas Primas, Vincent Remusat, Youssef Kabri, Clémence Tabélé, Patrice Vanelle, Christophe Curti
Publikováno v:
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2015, 47, pp.3339-3346. ⟨10.1055/s-0034-1381034⟩
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2015, 47, pp.3339-3346. ⟨10.1055/s-0034-1381034⟩
Synthesis: Journal of Synthetic Organic Chemistry, 2015, 47, pp.3339-3346. ⟨10.1055/s-0034-1381034⟩
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2015, 47, pp.3339-3346. ⟨10.1055/s-0034-1381034⟩
International audience; To obtain aromatic 2-methylallyl derivatives, cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids were studied. Among allylic alcohols described for such cross-coupling reactions, 2-methyl-2-prope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0865ba64332f72df0f15ca9a57bcae1
https://hal.science/hal-01423338/document
https://hal.science/hal-01423338/document
Autor:
Ahlem Bouhlel, Patrice Vanelle, Nicolas Primas, Vincent Remusat, Sébastien Hutter, Thierry Terme, Anita Cohen, Christophe Curti, Clémence Tabélé, Nadine Azas
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2014, 87, pp.440-453. ⟨10.1016/j.ejmech.2014.07.113⟩
European Journal of Medicinal Chemistry, 2014, 87, pp.440-453. ⟨10.1016/j.ejmech.2014.07.113⟩
European Journal of Medicinal Chemistry, Elsevier, 2014, 87, pp.440-453. ⟨10.1016/j.ejmech.2014.07.113⟩
European Journal of Medicinal Chemistry, 2014, 87, pp.440-453. ⟨10.1016/j.ejmech.2014.07.113⟩
International audience; Following the promising antileishmanial results previously obtained in monoamidoxime series, a new series of derivatives was synthesized using manganese(III) acetate, Wittig reactions and Suzuki-Miyaura cross coupling reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b24203e249373f5be32ce53c9d74ca5
https://hal.archives-ouvertes.fr/hal-01417043
https://hal.archives-ouvertes.fr/hal-01417043
Publikováno v:
Molecules, Vol 18, Iss 4, Pp 4293-4307 (2013)
A convenient microwave irradiation protocol was utilized for the synthesis of b-ketosulfones 1–5 in good yields. These sulfones reacted with alkenes through a radical oxidative cyclization mediated by Mn(OAc)3. Dihydrofurans 6–10 were obtained in
Externí odkaz:
https://doaj.org/article/3055f51816c94e64abaf6df82e704c9d