Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Leslie Duroure"'
Publikováno v:
Journal of Natural Products. 81:1946-1955
As part of a search for new sustainable plant sources of valuable compounds, the EtOAc extract of the discarded calyces of Physalis peruviana fruit was selected for its significant antiaging activity. Eight new sucrose esters (SEs), named peruvioses
Publikováno v:
Flavour and Fragrance Journal. 32:317-329
Essential oils and CO2 extracts of Timur (Zanthoxylum armatum DC syn. Zanthoxylum alatum Hemsl.) from fruits cropped in the Nepalese districts Surkhet, Jajarkot and Salyan from 2012 to 2015 were analysed to explain their typical odour and characteriz
Publikováno v:
European Journal of Organic Chemistry. 2014:7716-7720
The synthesis of chiral spiroimines, one of the pharmacophores of the marine neurotoxin gymnodimine A is described. The approach relies on a three-step sequence that includes a palladium-catalyzed asymmetric decarboxylative alkylation, an isomerizati
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2008, 10 (15), pp.3203-3206. ⟨10.1021/ol801025u⟩
Organic Letters, American Chemical Society, 2008, 10 (15), pp.3203-3206. ⟨10.1021/ol801025u⟩
International audience; We have developed an inexpensive catalytic system using a readily available copper/ligand combination for the Sonogashira-type cross-coupling of aryl iodides and phenyl- and hexyl-acetylene which affords disubstituted alkynes
Publikováno v:
ChemInform. 46
The synthesis of optically active spiroimines, one of the pharmacophores of the marine neurotoxin gymnodimine A, is described.
Autor:
Pascal Retailleau, Rómulo Aráoz, Leslie Duroure, Laurent Chabaud, Catherine Guillou, Thierry Jousseaume, Elvina Barre, Jordi Molgó
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2011, 9, pp.8112-8118. ⟨10.1039/c1ob06257c⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2011, 9 (23), pp.8112-8. ⟨10.1039/c1ob06257c⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2011, 9, pp.8112-8118. ⟨10.1039/c1ob06257c⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2011, 9 (23), pp.8112-8. ⟨10.1039/c1ob06257c⟩
International audience; Simple models of the spiroimine core of (-)-gymnodimine A have been synthesized in racemic and optically active forms. The quaternary carbon of the racemic spiroimines was created by Michael addition of a β-ketoester to acrol
Publikováno v:
ChemInform. 39