Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Maria A. Csiba"'
Publikováno v:
International journal of cosmetic scienceREFERENCES.
This article describes the eco-design of a new preservative in cosmetics based on bio-inspiration of natural extracts from traditional medicines. In order to reach the multiple specification targets, various structures have been synthesized and evalu
Autor:
Lisheng Mao, Francisco Alvarez, Sébastien Dropsit-Montovert, Long Lu, Maria Dalko-Csiba, Xavier Marat, Jinzhu Xu, Yudi Ding, Susana Ramos, Amélie Prévot-Guéguiniat, Florence Pic, Clément Aracil, Magali Lima, Marie-Céline Frantz
Publikováno v:
Organic Letters. 21:2684-2687
An efficient, divergent, and straightforward access to novel C-glycosides has been developed, namely, α-hydroxy carboxamide and carboxylic acid derivatives, via a green and scalable process from unprotected carbohydrates. The method involves condens
Autor:
Anne-Claude Dublanchet, Maude Brossat, Michel Philippe, Maria Dalko-Csiba, Julien Hitce, Jinzhu Xu, Marie-Céline Frantz
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 13:164-169
Sustainable innovation is a key-objective for our Group that has recently integrated the principles of sustainable development into all stages of a product's life cycle, from its design to consumer use. The following ambitious commitment: 100% of its
Autor:
Laurence Deyon-Jung, Christophe Morice, Florence Chéry, Julie Gay, Thierry Langer, Marie-Céline Frantz, Roger Rozot, Maria Dalko-Csiba
Publikováno v:
MedChemComm. 7:506-511
Through a process of fragmentation, functionalization, and recombination of market approved molecules for cosmetic usage, we customized an in-house virtual library comprising molecules ideally suited for virtual screening. Computational pharmacophore
Flash-metathesis for the coupling of sustainable (poly)hydroxyl β-methylstyrenes from essential oils
Publikováno v:
Green Chemistry. 17:3756-3761
A cross-metathesis procedure was developed to synthetize symmetrical and non symmetrical stilbenes from sustainable resources. The reaction proceeds under solvent-free conditions and at low catalyst loading (down to 0.01 mol%) within a couple of minu
Autor:
Sibylle Jäger, Christian Tran, Maria Dalko-Csiba, Anne-Marie Minondo, Jean-François Michelet, Florian Formanek, Philippe Bastien, Hugues Lortat-Jacob, Elodie Henriet, Lionel Breton, Romain R. Vivès
Publikováno v:
Biochimica et Biophysica Acta (BBA)-General Subjects
Biochimica et Biophysica Acta (BBA)-General Subjects, Elsevier, 2017, 1861 (9), pp.2250-2260. ⟨10.1016/j.bbagen.2017.06.006⟩
Biochimica et Biophysica Acta (BBA)-General Subjects, 2017, 1861 (9), pp.2250-2260. ⟨10.1016/j.bbagen.2017.06.006⟩
Biochimica et Biophysica Acta (BBA)-General Subjects, Elsevier, 2017, 1861 (9), pp.2250-2260. ⟨10.1016/j.bbagen.2017.06.006⟩
Biochimica et Biophysica Acta (BBA)-General Subjects, 2017, 1861 (9), pp.2250-2260. ⟨10.1016/j.bbagen.2017.06.006⟩
Background Jasmonates are plant hormones that exhibit anti-cancer and anti-inflammatory properties and have therefore raised interest for human health applications. The molecular basis of these activities remains poorly understood, although increasin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6801740c77589f5bebec0c67b0f94539
https://hal.archives-ouvertes.fr/hal-01553681
https://hal.archives-ouvertes.fr/hal-01553681
Autor:
Magali Lima, Xavier Marat, Clément Aracil, Jinzhu Xu, Lisheng Mao, Francisco Alvarez, Florence Pic, Maria Dalko-Csiba, Marie-Céline Frantz, Amélie Prévot-Guéguiniat, Sébastien Dropsit-Montovert, Susana Ramos, Long Lu, Yudi Ding
Publikováno v:
Organic Letters. 21:3470-3470
Autor:
Maria Dalko-Csiba, Michel Philippe, Jinzhu Xu, Maude Brossat, Anne-Claude Dublanchet, Julien Hitce, Marie-Céline Frantz
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 13:171
Publikováno v:
Chemistry - A European Journal. 16:6056-6068
Titrations of commercial diaminobutane (DAB) and polyamidoamine (PAMAM) dendrimers by vitamins C (ascorbic acid, AA), B(3) (nicotinic acid), and B(6) (pyridoxine) were monitored by (1)H NMR spectroscopy using the chemical shifts of both dendrimer and
Autor:
Christophe Boulle, Alexandre Cavezza, Amelie Gueguiniat, Patrick Pichaud, Louis Ricard, Simon Trouille, Maria Dalko-Csiba
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:845-849
The scope and limitation of Lubineau's reaction were evaluated for the synthesis of C-glycosides (compounds 1-13). Further transformation of side chain carbonyl was also achieved (compounds 16-23). Optimization of these two steps was investigated in