Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Elise Tran Huu Dau"'
Autor:
Cyril Poullain, Jean-Claude Guillemot, Bruno Canard, Françoise Guéritte, Marc Litaudon, Vincent Dumontet, Elise Tran Huu Dau, Pierre-Marie Allard, Cécilia Eydoux
Publikováno v:
Journal of Natural Products
Journal of Natural Products, American Chemical Society, 2011, 74 (11), pp.2446-53. ⟨10.1021/np200715v⟩
Journal of Natural Products, American Chemical Society, 2011, 74 (11), pp.2446-53. ⟨10.1021/np200715v⟩
International audience; An in vitro screening of New Caledonian plants allowed the selection of several species with a significant dengue virus NS5 RNA-dependent RNA polymerase (RdRp) inhibiting activity. The chemical investigation of Cryptocarya cha
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2009, 11 (18), pp.4044-7. ⟨10.1021/ol901452d⟩
Organic Letters, American Chemical Society, 2009, 11 (18), pp.4044-7. ⟨10.1021/ol901452d⟩
International audience; Reaction of an isoquinoline, a silyloxyfuran, and an acyl or sulfonyl chloride provides easy access to a wide variety of isoquinolinobutyrolactones with excellent yields and diastereoselectivites (R*,R* isomer), even in the ca
Autor:
Olivier Lafon, Marie-Elise Tran Huu Dau, Li Chen, Philippe Lesot, Françoise Dumas, Pierre Chaminade, André Loupy, Franck Le Bideau, Lai Wei, Lucie Vandromme
Publikováno v:
Proceedings of MOL2NET, International Conference on Multidisciplinary Sciences.
In connection with synthetic applications, we have foreseen to study the reactivity of the poorly reactive tert-butyl acrylate electrophile with chiral imines of unsymmetrical ketones, using conventional or microwave flash heating under carefully con
Autor:
Stéphanie Norsikian, Alexandre Cannillo, Jean-Marie Beau, Pascal Retailleau, Marie-Elise Tran Huu Dau, Bogdan I. Iorga
Publikováno v:
ChemInform. 46
A sequence combining Petasis and Diels—Alder reactions gives access to hexahydroisoindole scaffolds in a one-step procedure.
Autor:
Marie-Thérèse Martin, Diaa T. A. Youssef, Pierre Sauleau, Marie-Elise Tran Huu Dau, Marie-Lise Bourguet-Kondracki
Publikováno v:
Journal of Natural Products
Journal of Natural Products, American Chemical Society, 2006, 69 (12), pp.1676-9. ⟨10.1021/np060132r⟩
Journal of Natural Products, American Chemical Society, 2006, 69(12), pp.1676-1679. ⟨10.1021/np060132r⟩
Journal of Natural Products, American Chemical Society, 2006, 69 (12), pp.1676-9. ⟨10.1021/np060132r⟩
Journal of Natural Products, American Chemical Society, 2006, 69(12), pp.1676-1679. ⟨10.1021/np060132r⟩
International audience; Biological and chemical investigations of the methanolic crude extract of the Red Sea marine sponge Hyrtios erectus led to the isolation of a novel azepino-indole-type alkaloid named hyrtiazepine (2) and 5-hydroxy-1H-indole-3-
Autor:
Frederic Hendra, Christian Cavé, Mohammed Nour, Sandrine Delarue-Cochin, Mathieu Pizzonero, Françoise Dumas, Marie-Elise Tran Huu-Dau, Jean d'Angelo
Publikováno v:
Tetrahedron: Asymmetry
Tetrahedron: Asymmetry, Elsevier, 2005, 16 (23), pp.3853-3857. ⟨10.1016/j.tetasy.2005.10.034⟩
Tetrahedron: Asymmetry, Elsevier, 2005, 16 (23), pp.3853-3857. ⟨10.1016/j.tetasy.2005.10.034⟩
In contrast with keto diester ( R )- 10a bearing a methyl ester group at the quaternary carbon center, the benzyl ester analogue ( R )- 10a partially racemized during workup, thereby revealing that the nature of the ester group at the quaternary carb
An unprecedented outcome of the lithium–ammonia reduction of enones: the formation of cyclopropanols
Autor:
Cyrille Thominiaux, Didier Desmaële, Christine Miet, Christian Cavé, Jean d'Angelo, Marie-Elise Tran Huu-Dau, Mohammed Nour, Georges Morgant, Françoise Dumas
Publikováno v:
Tetrahedron Letters. 43:9649-9652
An unusual process takes place during the lithium–ammonia reduction of a variety of cyclic enones bearing an ester group in the γ-position, furnishing cyclopropanols. The reason for this unprecedented outcome has been attributed to the through-spa
Publikováno v:
The Journal of Organic Chemistry. 67:5408-5411
A general method giving access to protected alpha-alkyl amino glycines (A3G) 4 from the previously described precursor alpha-isopropylthioglycine 1 is described. In the presence of N-bromosuccinimide, displacement of the thiol by a large variety of a
Autor:
Jean-Marie Beau, Pascal Retailleau, Alexandre Cannillo, Marie-Elise Tran Huu Dau, Bogdan I. Iorga, Stéphanie Norsikian
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (38), pp.12133-12143. ⟨10.1002/chem.201402965⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (38), pp.12133-12143. ⟨10.1002/chem.201402965⟩
International audience; One-step assembly of hexahydroisoindole scaffolds by a sequence that combines the Petasis (borono-Mannich) and Diels-Alder reactions is described. The unique selectivity observed experimentally was confirmed by quantum calcula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28754013ad06ef6a7d27bb4b1d36aa43
https://hal.archives-ouvertes.fr/hal-01065678
https://hal.archives-ouvertes.fr/hal-01065678
Publikováno v:
ChemInform. 45
Benzotriazole is used as an efficient catalyst for transamidation reactions of amides, imides, and urea.