Green extraction of polyphenols from citrus peel by-products and their antifungal activity against Aspergillus flavus

Autor: Meryem Benohoud, Caroline Orfila, Yue Liu, Yun Yun Gong, Joseph Hubert Galani Yamdeu

Publikováno v: Food Chemistry: X
Food Chemistry: X, Vol 12, Iss, Pp 100144-(2021)

Highlights • Mandarin peel extracts inhibited the growth of A. flavus by up to 52% over 7 days. • The MIC of mandarin extracts was 300-400 mg mL−1 depending on the extraction solvent. • Phenolic-rich SPE fractions showed 40% higher antifungal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8b2845d4b765bb7d9c32daf39128db5
http://europepmc.org/articles/PMC8566929

Starch Digestion Enhances Bioaccessibility of Anti-Inflammatory Polyphenols from Borlotti Beans (

Autor: Lucia Margarita, Perez-Hernandez, Kartika, Nugraheni, Meryem, Benohoud, Wen, Sun, Alan Javier, Hernández-Álvarez, Michael R A, Morgan, Christine, Boesch, Caroline, Orfila

Publikováno v: Nutrients

The consumption of beans has been associated with chronic disease prevention which may be attributed to the polyphenols present in the seed coat and endosperm. However, their bioaccessibility is likely to be limited by interactions with bean matrix c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::edd2c44a69250ad21857ecb535e59ee9
https://pubmed.ncbi.nlm.nih.gov/31978996

A New Supported Reagent for the Parallel Synthesis of Primary and Secondary O-Alkyl Hydroxylamines through a Base-Catalyzed Mitsunobu Reaction

Autor: Ludovic T. Maillard, Bernard Badet, Philippe Durand, Meryem Benohoud

Publikováno v: ResearcherID
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2005, 70, pp.6303-6312. ⟨10.1021/jo050722⟩

International audience; The growing field of applications of O-alkyl hydroxylamines in medicinal chemistry and chemical biology has motivated the search for a parallel synthesis. A solid-phase approach based on the alkylation by alcohols of a new sup

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dade2d7d41e9d7a2d996f055b270ea5
https://doi.org/10.1021/jo050722e

Catalytic enantioselective [4 + 2]-cycloaddition: a strategy to access aza-hexacycles

Autor: Meryem Benohoud, Claudia Lalli, Guillaume Dagousset, Géraldine Masson

Publikováno v: Chemical Society Reviews
Chemical Society Reviews, Royal Society of Chemistry, 2013, 42 (3), pp.902-23. ⟨10.1039/c2cs35370a⟩

International audience; The aza-Diels Alder reaction has become one of the most widely used synthetic tools for the preparation of N-containing 6-membered heterocycles. Numerous important developments have been reported to render this reaction cataly

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b3fc7e96090d035bed56f055eb78a52
https://pubmed.ncbi.nlm.nih.gov/23172010

Total synthesis and absolute configuration of the natural amino acid tetrahydrolathyrine

Autor: Sílvia Helena Cardoso, Meryem Benohoud, Philippe Dauban, Loïc Leman, Robert H. Dodd, Josiane Thierry, Pascal Retailleau

Publikováno v: Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2009, 74 (15), pp.5331-6. ⟨10.1021/jo900800x⟩

International audience; The natural product tetrahydrolathyrine has been synthesized through an iminoiodane-mediated aziridination of a (2S)-allylglycinol derivative, which provided a 2:3 mixture of diastereoisomers. One of these diastereoisomers was

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36da8af02bec122e8a3589eeab3923f
https://pubmed.ncbi.nlm.nih.gov/19572523