Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Nicolas Birlirakis"'
Autor:
Samuel Oger, Nicolas Duchemin, Yara Mayssa Bendiab, Nicolas Birlirakis, Adam Skiredj, Somia Rharrabti, Jean-Christophe Jullian, Erwan Poupon, Michael Smietana, Stellios Arseniyadis, Laurent Evanno
Publikováno v:
Chemical Communications. 59:4221-4224
We report here a general and scalable method for the synthesis of cyclobutane-containing natural products and analogues thereof via a DNA-templated [2+2] photo-induced homo- and heterodimerization of aplysinopsins.
Autor:
Mohamad Nurul Azmi, Charlotte Gény, Aurélie Leverrier, Marc Litaudon, Vincent Dumontet, Nicolas Birlirakis, Françoise Guéritte, Kok Hoong Leong, Siti Nadiah Abd. Halim, Khalit Mohamad, Khalijah Awang
Publikováno v:
Molecules, Vol 19, Iss 2, Pp 1732-1747 (2014)
A phytochemical investigation of the methanolic extract of the bark of Endiandra kingiana led to the isolation of seven new tetracyclic endiandric acid analogues, kingianic acids A–G (1–7), together with endiandric acid M (8), tsangibeilin B (9)
Externí odkaz:
https://doaj.org/article/4b75c19196064d12bce9adff01360927
Autor:
Nicolas Birlirakis, Marc Litaudon, Jérôme Bignon, Vincent Dumontet, Eric Guittet, Gwladys Rivière, Charlotte Gény, Khaljah Awang, Fanny Roussi
Publikováno v:
Journal of Natural Products
Journal of Natural Products, 2016, 79 (4), pp.838-844. ⟨10.1021/acs.jnatprod.5b00915⟩
Journal of Natural Products, American Chemical Society, 2016, 79 (4), pp.838-844. ⟨10.1021/acs.jnatprod.5b00915⟩
Journal of Natural Products, 2016, 79 (4), pp.838-844. ⟨10.1021/acs.jnatprod.5b00915⟩
Journal of Natural Products, American Chemical Society, 2016, 79 (4), pp.838-844. ⟨10.1021/acs.jnatprod.5b00915⟩
International audience; Proteins of the Bcl-2 family are key targets in anticancer drug discovery. Disrupting the interaction between anti and pro-apoptotic members of this protein family was the approach chosen in this study to restore apoptosis. Th
Publikováno v:
Nature Chemistry. 4:663-667
Although arguably the most important reaction in glycoscience, chemical glycosylations are among the least well understood of organic chemical reactions, resulting in an unnecessarily high degree of empiricism and a brake on rational development in t
Publikováno v:
Biomolecular NMR Assignments
Biomolecular NMR Assignments, Springer, 2013, 7 (1), pp.1-4. ⟨10.1007/s12104-012-9364-3⟩
Biomolecular NMR Assignments, Springer, 2013, 7 (1), pp.1-4. ⟨10.1007/s12104-012-9364-3⟩
International audience; CGC-19, a 14 kDa proteic constituent of a non ribosomal peptide synthetase implicated in the biosynthesis of a secondary metabolite in Streptomyces ambofaciens, has been isotopically enriched and recombinantly expressed. Its n
Autor:
Talbi Kaoudi, Nicolas Birlirakis, Imad Safir, Susana Porcel, Loïc Toupet, Isabel Castellote, Siméon Arseniyadis
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2006, 12(28), pp.7337-7344. ⟨10.1002/chem.200600494⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2006, 12(28), pp.7337-7344. ⟨10.1002/chem.200600494⟩
Oxidative cleavage with lead tetraacetate results in the synthesis of different oxygen heterocycles starting from the same unsaturated 1,2-diol of type I by tuning of the substitution pattern at the angular position. When this compound bears a functi
Autor:
Jacques Einhorn, A. Cingöz, Loïc Lepiniec, Nicolas Birlirakis, Jean-Marc Routaboul, Denya Aouak, Lucien Kerhoas
Publikováno v:
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry, American Chemical Society, 2006, 54 (18), pp.6603-6612. ⟨10.1021/jf061043n⟩
Journal of Agricultural and Food Chemistry, American Chemical Society, 2006, 54(18), pp.6603-6612
Journal of Agricultural and Food Chemistry, American Chemical Society, 2006, 54 (18), pp.6603-6612. ⟨10.1021/jf061043n⟩
Journal of Agricultural and Food Chemistry, American Chemical Society, 2006, 54(18), pp.6603-6612
International audience; Information gains from the seed of the model plant Arabidopsis thaliana( Brassicaceae) have greatly contributed to a better understanding of flavonoid synthesis and may be used for crop improvement. However, exhaustive identif
Autor:
José Ignacio Candela Lena, Jose Ignacio Martin Hernando, Maria del Rosario Rico Ferreira, Sylvain Loïc Jean-Luc Hamon, José Quilez del Moral, Loï C Toupet, Nicolas Birlirakis, Siméon Arseniyadis
Publikováno v:
Tetrahedron: Asymmetry. 16:3241-3255
Central intermediate 5 for the taxoid diterpene framework, prepared by the aldol–annulation sequence, permitted the construction of A-secotaxane frameworks incorporating differentiatable olefin and oxygen functionalities suitable for further elabor
Publikováno v:
European Journal of Organic Chemistry. 2005:4082-4092
The goal of this investigation is to assemble the 20-carbon unit 1 of the taxoid diterpene skeleton with a high level of stereocontrol by means of a three-reaction sequence developed in this laboratory. The strategy involves seven C–C bond-forming
Autor:
José Ignacio Candela Lena, Ertan Altinel, Nicolas Birlirakis, Özge Sesenoglu, Siméon Arseniyadis
Publikováno v:
Tetrahedron: Asymmetry. 16:995-1015
The effect of solvent on oxidative cleavage of the Hajos–Parrish ketone derived hydrindene–diols 1 , and Wieland–Miescher ketone derived octaline–diols 2 with Pb(OAc) 4 is presented. Various solvents were screened and compared for these domin