Co-auteurs

Nombre de documents

25

Pr. Frédéric Guillen


Article dans une revue25 documents

  • Asmae Kaoukabi, Frédéric Guillen, Hicham Qayouh, Asmaa Bouyahya, Sébastien Balieu, et al.. The use of ionic liquids as an organocatalyst for controlled ring-opening polymerization of ϵ-caprolactone. Industrial Crops and Products, Elsevier, 2015, sous presse. <10.1016/j.indcrop.2015.02.002>. <hal-01140371>
  • Delphine Brégeon, Laurent Ferron, Antony Chrétien, Frédéric Guillen, Viacheslav Zgonnik, et al.. Synthesis of phosphoantigens: scalable accesses to enantiomers of BrHPP and studies on N-HDMAPP synthesis.. Bioorganic & Medicinal Chemistry Letters, Elsevier, 2012, 22 (18), pp.5807-5810. <10.1016/j.bmcl.2012.07.092>. <hal-00996932>
  • Viacheslav Zgonnik, Silvia Gonella, Marie-Rose Mazières, Frédéric Guillen, Gérard Coquerel, et al.. Design and scalable synthesis of new chiral selectors. Part 2: Chiral ionic liquids derived from diaminocyclohexane and histidine. Organic Process Research & Development, 2012, pp.277-285. <10.1021/op200082a>. <hal-01016032>
  • Hicham Iken, Frédéric Guillen, Helene Chaumat, Marie-Rose Mazières, Jean-Christophe Plaquevent, et al.. Scalable synthesis of ionic liquids: comparison of performances of microstructured and stirred batch reactors. Tetrahedron Letters, Elsevier, 2012, pp.3474-3477. <10.1016/j.tetlet.2012.04.119>. <hal-01016015>
  • Annie-Claude Gaumont, Y. Genisson, F. Guillen, Jean-Christophe Plaquevent. De Pasteur aux liquides ioniques chiraux Petite histoire de l'induction asymétrique promue par le solvant. L'Actualité Chimique, 2011, pp.84-89. <hal-01016584>
  • Laurent Ferron, Frédéric Guillen, Servane Coste, Gérard Coquerel, Pascal Cardinaël, et al.. Design and scalable synthesis of new chiral selectors. Part 1: Synthesis and characterization of a new constrained cyclopeptide from unnatural bulky amino acids. Tetrahedron, Elsevier, 2011, pp.6036-6044. <10.1016/j.tet.2011.06.032>. <hal-01016393>
  • Zhor El Asri, Yves Génisson, Frédéric Guillen, Olivier Baslé, Nicolas Isambert, et al.. Multicomponent reactions in ionic liquids: convenient and ecocompatible access to the 2,6-DABCO core. Green Chemistry, Royal Society of Chemistry, 2011, 13, pp.2549-2552. <10.1039/c1gc15635g>. <hal-00681302>
  • Annie-Claude Gaumont, Yves Génisson, Frédéric Guillen, Jean-Christophe Plaquevent. De Pasteur aux liquides ioniques chiraux Petite histoire de l’induction asymétrique promue par le solvant. L'Actualité Chimique, 2011, 348-349, pp.84-89. <hal-01139859>
  • Matthieu Pepin, Marie Hubert-Roux, Claudette Martin, Frédéric Guillen, Catherine Lange, et al.. First Examples of α-(1→4)-Glycosylation Reactions on Ionic Liquid Supports. European Journal of Organic Chemistry, Wiley-VCH Verlag, 2010, pp.6366-6371. <10.1002/ejoc.201000754>. <hal-01022123>
  • Guillaume Levilain, Céline Rougeot, Frédéric Guillen, Jean-Christophe Plaquevent, Gérard Coquerel. Attrition-enhanced preferential crystallization combined with racemization leading to redissolution of the antipode nuclei. Tetrahedron: Asymmetry, Elsevier, 2009, 20 (24), pp.2769. <10.1016/j.tetasy.2009.11.015>. <hal-01147124>
  • Guillaume Mercey, Delphine Brégeon, Christine Baudequin, Frédéric Guillen, Jocelyne Levillain, et al.. Thiazolinium salt: an efficient catalyst for the Mukaiyama reaction. Tetrahedron Letters, Elsevier, 2009, 50 (52), pp.7239. <10.1016/j.tetlet.2009.09.168>. <hal-01147118>
  • James Ternois, Frédéric Guillen, Guy Piacenza, Sébastien Rose, Jean-Christophe Plaquevent, et al.. Towards a Robust and Reliable Method for the Reduction of Functionalized Sulfoxides. Organic Process Research and Development, American Chemical Society, 2008, 12 (4), pp.614. <10.1021/op800088x>. <hal-01147104>
  • D. Brégeon, J. Levillain, F. Guillen, J.-C. Plaquevent, A.-C. Gaumont. Thiazolinium and imidazolium chiral ionic liquids derived from natural amino acid derivatives. Amino Acids, Springer Verlag, 2008, 35 (1), pp.175. <10.1007/s00726-007-0575-3>. <hal-01147106>
  • James Ternois, Frédéric Guillen, Jean-Christophe Plaquevent, Gérard Coquerel. Asymmetric synthesis of modafinil and its derivatives by enantioselective oxidation of thioethers: comparison of various methods including synthesis in ionic liquids. Tetrahedron: Asymmetry, Elsevier, 2007, 18 (24), pp.2959. <10.1016/j.tetasy.2007.11.031>. <hal-01147092>
  • Laurent Ferron, Frédéric Guillen, Servane Coste, Gérard Coquerel, Jean-Christophe Plaquevent. Is the optical rotation sign/absolute configuration relationship still a problem? Examples taken from unnatural quaternary aminoacids. Chirality, Wiley, 2006, 18 (8), pp.662. <10.1002/chir.20296>. <hal-01147079>
  • Frédéric Guillen, Delphine Brégeon, Jean-Christophe Plaquevent. (S)-Histidine: the ideal precursor for a novel family of chiral aminoacid and peptidic ionic liquids. Tetrahedron Letters, Elsevier, 2006, 47 (8), pp.1245. <10.1016/j.tetlet.2005.12.090>. <hal-01147084>
  • Caroline L. Winn, Frédéric Guillen, Julien Pytkowicz, Sylvain Roland, Pierre Mangeney, et al.. Enantioselective copper catalysed 1,4-conjugate addition reactions using chiral N-heterocyclic carbenes. Journal of Organometallic Chemistry, Elsevier, 2005, 690 (24-25), pp.5672. <10.1016/j.jorganchem.2005.07.024>. <hal-01147004>
  • Hélène Vallette, Laurent Ferron, Gérard Coquerel, Frédéric Guillen, Jean-Christophe Plaquevent. Room temperature ionic liquids (RTIL’s) are convenient solvents for peptide synthesis!. ARKIVOC - Online Journal of Organic Chemistry, Arkat USA Inc, 2005, 2006 (4), pp.200. <10.3998/ark.5550190.0007.414>. <hal-01147069>
  • Christine Baudequin, Delphine Brégeon, Jocelyne Levillain, Frédéric Guillen, Jean-Christophe Plaquevent, et al.. Chiral ionic liquids, a renewal for the chemistry of chiral solvents? Design, synthesis and applications for chiral recognition and asymmetric synthesis. Tetrahedron: Asymmetry, Elsevier, 2005, 16 (24), pp.3921. <10.1016/j.tetasy.2005.10.026>. <hal-01147043>
  • Michaël Rivard, Frédéric Guillen, Jean-Claude Fiaud, Christie Aroulanda, Philippe Lesot. Efficient enantiodiscrimination of chiral monophosphine oxides and boranes by phosphorus coupled 13C NMR spectroscopy in the presence of chiral ordering agents. Tetrahedron: Asymmetry, Elsevier, 2003, 14 (9), pp.1141. <10.1016/S0957-4166(03)00202-7>. <hal-01146992>
  • Alexandre Alexakis, Caroline l. Winn, Frédéric Guillen, Julien Pytkowicz, Sylvain Roland, et al.. Asymmetric Synthesis withN-Heterocyclic Carbenes. Application to the Copper-Catalyzed Conjugate Addition. Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2003, 345 (3), pp.345. <10.1002/adsc.200390037>. <hal-01146999>
  • Frédéric Guillen, Michael Rivard, Martial Toffano, Jean-Yves Legros, Jean-Claude Daran, et al.. Synthesis and first applications of a new family of chiral monophosphine ligand: 2,5-diphenylphosphospholanes. Tetrahedron, 2002, 58 (29), pp.5895. <10.1016/S0040-4020(02)00554-9>. <hal-01146983>
  • Alexandre Alexakis, Stéphane Rosset, Janik Allamand, Sébastien March, Frédéric Guillen, et al.. Novel Biphenol Phosphoramidite Ligands for the Enantioselective Copper-Catalyzed Conjugate Addition of Dialkyl zincs. SYNLETT, Georg Thieme Verlag, 2001, 2001 (09), pp.1375. <10.1055/s-2001-16791>. <hal-01146967>
  • Frédéric Guillen, Caroline L. Winn, Alexandre Alexakis. Enantioselective copper-catalyzed conjugate addition using chiral diaminocarbene ligands. Tetrahedron: Asymmetry, Elsevier, 2001, 12 (15), pp.2083. <10.1016/S0957-4166(01)00387-1>. <hal-01146973>
  • Frédéric Guillen, Jean-Claude Fiaud. Enantiomerically pure 1,2,5-triphenylphospholane through the synthesis and resolution of the chiral trans-(2,5)-diphenylphospholanic acid. Tetrahedron Letters, Elsevier, 1999, 40 (15), pp.2939. <10.1016/S0040-4039(99)00329-9>. <hal-01146949>