Laboratoire de Chimie Moléculaire et Thio-organique

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Publications

Les publications du LCMT

Séminaires

Les séminaires du LCMT

Livres

C-H bond functionalization
Elie, M.; Renaud, J-L.; Gaillard, S.
in Sciences of Synthesis, Thieme, N-Heterocyclic Carbenes in Catalytic Organic Synthesis 1, N. P. Nolan, C. S. J. Cazin Eds, Georg Thieme Verlag, Stuttgart, 2017, 199-260.

Luminescent Cationic Copper(I) Complexes: Synthesis, Photophysical Properties and Application in Light-Emitting Electrochemical Cells
Elie, M.; Renaud, J-L.;  Gaillard, S.
in Light-Emitting Electrochemical Cells: Concepts, Advances and Challenges, Costa, R. D. Ed., Springer International Publishing, 2017, 287-327.

Quantitative Treatment of Nucleophilicity and Lewis Basicity (book Chapter)
Lakhdar, S.
In Lewis Base Catalysis in Organic Synthesis, Edwin Vedejs & Scott Denmark
(eds.) -Wiley-VCH, 2016.

Syntheses of Monofluoroalkyl compounds by substitution reactions
Lequeux, T.
In Science of Synthesis, volume 34 Compounds with One Carbon-Heteroatom  Bond: Fluorine, Editeurs J. F. Paquin, Houben-Weyl, 2016, chapitre 34-1-4-1 up-date

Activated Zeolites and Heteropolyacids Have Efficient Catalysts for Synthesis Without Use of Organic Solvent at Room Temperature
Hammadi, M.; Dokari, H.; Villemin, D.; Benferrah, N.
In Progress in Clean Energy, Springer, 2015 ed.; Ibrahim Dincer,C. Ozgur Colpan,Onder Kizilkan,M. Akif Ezan: 2015; pp 535-549.

Olefin metathesis in ionic liquids
Queval, P.;  Rouen, M.;  Gaumont, A.-C.; Dez, I.; Baslé, O.; M. Mauduit, M.
in Olefin Metathesis: Theory and Practice (Ed.: Karol Grela), John Wiley & Sons, 2014, p. 547-558.

Copper-catalyzedformation of C-P bonds with aryl halides
Alayrac,C.; Gaumont, A.-C.
In Copper-Mediated Cross Coupling Reactions G. Evano and N. Blanchard ed.; Wiley: Hoboken (New jersey), 2014; pp 93-111.

Reduction of S=O and SO2 toS, S-X to S-H, and P=O to P
Gaumont,A.-C.; Gulea, M.; Perrio, S.; Reboul, V.
In Comprehensive Organic Synthesis, Gary A.Molander and Paul Knochel ed.; Elsevier: Oxford, 2014; Vol. 8, pp 535-563.

Methyl Lithiodithioacetate
Perrio,S.
In e-eros Electronic Encyclopedia of Reagents for Organic Synthesis, B. A. Charrette Ed. ;Wiley: 2014; pp1-12.

Application to the synthesis of natural products
Witulski, B.; Grand, J.
In Transition-Metal-Mediated Aromatic Ring Construction, K. Tanaka ed.; Wiley: Hoboken (New Jersey), 2013; pp 207-242.

Chloro[(1R,2S)-2,3-dihydro-1-[[[2-(hydroxy-O)-5-methyl-3-tricyclo[3.3.1.13,7dec-1-ylphenyl]methyl-ene]amino-N]-1H-indene-2-olato-(2-)-O] chromium
J.-L. Renaud, S. Gaillard
e-EROS Electronic Encyclopedia of Reagents for Organic Synthesis, 2012.

Two new graph kernels and applications to chemoinformatics
B. Gaüzère, L.  Brun, D. Villemin
Graph-based Representations in Pattern Recognition, GBR’11. vol. 6658, X. Jiang, M. Ferrer, A. Torsello edn: Springer; 2011: 112-121.

Chiral Ionic LIquids for asymmetric reactions
A.-C. Gaumont, Y. Genisson, F.  Guillen, V. Zgonnik, J.-C. Plaquevent
Catalytic methods in asymmetric synthesis Advances materials, techniques and applications. M. Gruttadauria and F. Giacalone edn.Wiley; 2011.

Recent Developments in the Synthesis of Dihydropyridines (DHP’s) and Dihydropyrimidines (DHPM’s)
J. Moreau,  J.-P. Hurvois, M. D. Mbaye, J.-L. Renaud
Targets in heterocyclic systems, chemistry and properties. O. Attanasi and D. Spinelli edn. Cambridge: Royal Society of Chemistry, 2010, Vol 12.

Epoxy-based Nanocomposites
L. Le  Pluart
Recent Advances in Polymer Nanocomposites: Synthesis and Characterization. S. Thomas,  S. V. Valsaraj, A. P. Meera, G. E. Zaikov edn. Leiden (The Netherlands): Brill Academic; 2010: 74-136.

(9R)-Amino-9-deoxyquinidine.
M.-C. Lasne, J. Rouden
e-EROS Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Ltd, Chichester, UK., 2009.

Fluorine-18 Chemistry for Molecular Imaging with Positron Emission Tomography in Fluorine and Health.
F. Dollé, D. Roeda, B. Kuhnast, M.-C. Lasne
Fluorine and Health,
Elsevier, Amsterdam, 2008, Vol. I – Chap.1, p. 3-65.

9-Phosphabicyclo[3.3.1]nonane, 9-cyclohexyl
O. Delacroix, A.-C. Gaumont
e-eros Electronic Encyclopedia of Reagents for Organic Synthesis, 2008.

Boron, (diphenylphosphine)trihydro
O. Delacroix, A.-C. Gaumont
e-eros Electronic Encyclopedia of Reagents for Organic Synthesis, 2008.

Synthesis and Use of Chiral Sulfur Ylides
Jean-François Brière, Patrick Metzner
Organosulfur Chemistry in Asymmetric Synthesis, Wiley-VCH, Weinheim, 2008, p. 179-208.

Electrophilic Fluorination with N-F Reagents
J Baudoux, D. Cahard
Organic Reactions, John Wiley & Sons, Ltd, 2008, Vol. 69, p. 347-673.

Arenesulfenic Acids and Derivatives
Stéphane Perrio, Vincent Reboul, Patrick Metzner
Science of Synthesis, Houben-Weyl, Methods of Molecular Transformations,
Thieme, Stuttgart, 2007, Vol. 31, p. 1043-1086.

Thio-Claisen Rearrangement
Stéphane Perrio, Vincent Reboul, Carole Alayrac, Patrick Metzner
Claisen Rearrangements, Wiley-VCH, Weinheim, 2007, p. 431-459.

O, O-Diethyl Phosphonodifluoromethyllithium
T. Lequeux, D. J. Burton, N. Qiu
e-eros Encyclopedia of Reagents for Organic Synthesis, John Wiley, Chichester, 2007, DOI: 10.1002/9780470842898.rd158.pub2.

2,2,2-Trifluoroethyl Diphenylphosphine Oxide
L. Jean-Baptiste, T. Lequeux
e-eros Encyclopedia of Reagents for Organic Synthesis, John Wiley & Sons, Chichester, 2007, DOI: 10.1002/9780470842898.rn00707.

Alk-1-enyl Phosphorus Compounds
M. Gulea, A.-C. Gaumont
Science of Synthesis, Houben-Weyl, Methods of Molecular Transformations, Thieme, Stuttgart, 2007, Vol. 33, p. 665-736.

Plant Protein-based Nanoparticles. Nanotechnologies for the Life Sciences
A.-M. Orecchioni, C. Duclairoir, J. Irache, E. Nakache
Biological and Pharmaceutical Nanomaterials, Willey-VCH, Weinheim, 2006, Vol. 2, p. 117-137.

Synthesis by Substitution of Oxygen and Sulfur Functionalities
T. Lequeux
Science of Synthesis, HoubenWeyl, Methods of Molecular Transformations, Thieme, Stuttgart, 2006, Vol. 34, p. 149-168.

Synthesis by Substitution of Heteroatoms
T. Lequeux
Science of Synthesis, HoubenWeyl, Methods of Molecular Transformations, Thieme, Stuttgart, 2006, Vol. 34, p. 57-70.

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