Jean-Pierre Baltaze
Centre national de la recherche scientifique
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Featured researches published by Jean-Pierre Baltaze.
Journal of Organic Chemistry | 2009
Ramzi Aït Youcef; Mickaël Dos Santos; Sandrine Roussel; Jean-Pierre Baltaze; Nadège Lubin-Germain; Jacques Uziel
Carbonated analogues of ribavirin were synthesized from ethyl C-ribosylpropiolate obtained by an alkynylation reaction mediated by indium(0). The C-ribosides were then engaged in a Huisgen 1,3-dipolar cycloaddition reaction under a micellar catalysis. In these conditions, formation of 1,2,3-triazoles with control of the regioselectivity was observed. The regiochemistry of the adducts was determined by HMBC 2D-NMR analysis.
Organic Letters | 2008
Nadège Lubin-Germain; Jean-Pierre Baltaze; Alexis Coste; Agnes Hallonet; Hugo Laureano; Grégory Legrave; Jacques Uziel; Jacques Augé
Indium-mediated alkynylation reaction was studied for the direct preparation of C-glycosides. Easily available starting sugar derivatives with an acetyl group at the anomeric position were tested as electrophiles toward alkynylindium reagents under Barbier conditions. Good yields and stereoselectivities were observed during the reaction. The alkynylation was applied to the synthesis of an alpha-(1-->6)-C-disaccharide analogue of isomaltoside.
Chemsuschem | 2015
Daniel Ortiz; Isabel Jiménez Gordon; Jean-Pierre Baltaze; Oscar Hernandez‐Alba; Solène Legand; Vincent Dauvois; Gregory Si Larbi; Uli Schmidhammer; Jean-Louis Marignier; Jean‐Frédéric Martin; J. Belloni; Mehran Mostafavi; Sophie Le Caër
The ageing phenomena occurring in various diethyl carbonate/LiPF6 solutions are studied using gamma and pulse radiolysis as a tool to generate similar species as the ones occurring in electrolysis of Li-ion batteries (LIBs). According to picosecond pulse radiolysis experiments, the reaction of the electron with (Li(+), PF6(-)) is ultrafast, leading to the formation of fluoride anions that can then precipitate into LiF(s). Moreover, direct radiation-matter interaction with the salt produces reactive fluorine atoms forming HF(g) and C2H5F(g). The strong Lewis acid PF5 is also formed. This species then forms various R(1)R(2)R(3) P=O molecules, where R is mainly -F, -OH, and -OC2H5. Substitution reactions take place and oligomers are slowly formed. Similar results were obtained in the ageing of an electrochemical cell filled with the same model solution. This study demonstrates that radiolysis enables a description of the reactivity in LIBs from the picosecond timescale until a few days.
European Polymer Journal | 2011
Bénédicte Lepoittevin; Xiaolu Wang; Jean-Pierre Baltaze; Hefang Liu; Jean-Marie Herry; Marie-Noëlle Bellon-Fontaine; Philippe Roger
Organic and Biomolecular Chemistry | 2012
Sophie Thétiot-Laurent; Francelin Bouillère; Jean-Pierre Baltaze; François Brisset; Debby Feytens; Cyrille Kouklovsky; Emeric Miclet; Valérie Alezra
Carbohydrate Polymers | 2011
Bénédicte Lepoittevin; Amina Elhiri; Loïc Bech; Joël Belleney; Jean-Pierre Baltaze; Isabelle Capron; Véronique Planchot; Philippe Roger
Journal of Power Sources | 2016
Daniel Ortiz; Isabel Jiménez Gordon; Solène Legand; Vincent Dauvois; Jean-Pierre Baltaze; Jean-Louis Marignier; Jean-Frédéric Martin; J. Belloni; Mehran Mostafavi; Sophie Le Caër
ChemistrySelect | 2016
Thi‐Thuy‐Duong Ngo; Kenta Kishi; Makoto Sako; Masashi Shigenobu; Chloée Bournaud; Martial Toffano; Régis Guillot; Jean-Pierre Baltaze; Shinobu Takizawa; Hiroaki Sasai; Giang Vo-Thanh
Synlett | 2013
Annie Pouilhes; Jean-Pierre Baltaze; Cyrille Kouklovsky
Chemsuschem | 2015
Daniel Ortiz; Isabel Jiménez Gordon; Jean-Pierre Baltaze; Oscar Hernandez‐Alba; Solène Legand; Vincent Dauvois; Gregory Si Larbi; Uli Schmidhammer; Jean-Louis Marignier; Jean-Frédéric Martin; J. Belloni; Mehran Mostafavi; Sophie Le Caër