Image
Téléphone
05 40 00 62 83
Groupe de recherche
Catalysis, Synthesis and Health
Statut
Permanent
Poste
Enseignant-chercheur
Batiment
A12
Etage
1° Ouest
Parcours
2000-Présent : Professeur des Universités, Université de Bordeaux
1995-2000 : Chargé de Recherches CNRS 1ère Classe, Université Bordeaux 1, Pr. M. Pereyre.
1994-1995 : Associate Research Fellow, Christopher Ingold Laboratories, University College London (Great-Britain), Pr. W.B. Motherwell.
1991-1994 : Chargé de Recherches CNRS 2ème Classe, Bordeaux 1 University, Pr. M. Pereyre.
1988-1991 : Doctorat de l’Ecole Polytechnique, Palaiseau, Dr. S. Z. Zard.
1986-1987 : D.E.A. de l’Université Paul Sabatier, Toulouse, Dr B. Meunier
Contact
eric.fouquet@u-bordeaux.fr
ISM, UMR-CNRS 5255, Groupe CSH, Université de Bordeaux,
Bât. A12, 351, cours de la libération, 33405 TALENCE Cedex
Publications
(). Benzisoselenazoles as Selenophenolate Anion Surrogates for the Formation of Carbon-Selenium Bonds via the Selena-Kemp Reaction. In Journal of Organic Chemistry (Vol. 89, Issue 15, p. 10462-10466). https://doi.org/10.1021/acs.joc.4c00581
(). 18F-Fluorination of a supported 2-(aryl-di-tert-butylsilyl)-N-methyl-imidazole for indirect 18F-labeling of a VH H single-variable domain. In Journal of Labelled Compounds and Radiopharmaceuticals (Vol. 67, Issue 3, p. 104-110). https://doi.org/10.1002/jlcr.4082
(). Ex Situ Generation of 18O2 and 17O2 from Endoperoxides for *O-Labeling and Mechanistic Studies of Oxidations by Dioxygen. In Organic Letters (Vol. 25, Issue 25, p. 4661-4665). https://doi.org/10.1021/acs.orglett.3c01487
(). Last-step 18F-fluorination of supported 2-(aryl-di-tert-butylsilyl)-N-methyl-imidazole conjugates for applications in positron emission tomography. In Chemical Communications (Vol. 58, Issue 65, p. 9140-9143). https://doi.org/10.1039/d2cc03258a
(). Biorecognition and detection of antigens from Mycobacterium tuberculosis using a sandwich ELISA associated with magnetic nanoparticles. In Journal of Pharmaceutical and Biomedical Analysis (Vol. 215, p. 114749). https://doi.org/10.1016/j.jpba.2022.114749
(). Synthesis and [*C]CO-labelling of (C,N)gem-dimethylbenzylamine-palladium complexes for potential applications in positron emission tomography. In Dalton Transactions (Vol. 50, Issue 30, p. 10608-10614). https://doi.org/10.1039/d1dt01633d
(). The Metallocene Battery: Ultrafast Electron Transfer Self Exchange Rate Accompanied by a Harmonic Height Breathing. In Angewandte Chemie - International Edition (Vol. 60, Issue 24, p. 13554-13558). https://doi.org/10.1002/anie.202100174
(). Practical synthesis of 13C-labeled conjugates by [13C]CO-carbonylation of supported arylbipyridylpalladium complexes and alkyne–azide cycloadditions. In Applied Organometallic Chemistry (Vol. 34, Issue 9, p. e5779). https://doi.org/10.1002/aoc.5779
(). Synthesis, characterization and bio-functionalization of magnetic nanoparticles to improve the diagnosis of tuberculosis. In Nanotechnology (Vol. 31, Issue 17, p. 175101). https://doi.org/10.1088/1361-6528/ab6ab1
(). Syntheses of o-iodobenzyl alcohols‒BODIPY structures as potential precursors of bimodal tags for positron emission tomography and optical imaging. In Tetrahedron (Vol. 75, Issue 52, p. 130765). https://doi.org/10.1016/j.tet.2019.130765
(). Expedient synthesis of a symmetric cycloheptyne-Co2 (CO)6 complex for orthogonal Huisgen cycloadditions. In Organic Chemistry Frontiers (Vol. 6, Issue 8, p. 1114-1117). https://doi.org/10.1039/c9qo00086k
(). Bioconjugated arylpalladium complexes on solid supports for a convenient last-step synthesis of 11C-labelled tracers for positron emission tomography. In Chemical Communications (Vol. 55, Issue 53, p. 7587-7590). https://doi.org/10.1039/c9cc03215k
(). Stabilization of a new nanocomposite family by reduction of gold nanoclusters with electron-reservoir complexes. In Chemical Communications (Vol. 55, Issue 69, p. 10277-10280). https://doi.org/10.1039/c9cc05260g
(). Cobaltocene Reduction of Cu and Ag Salts and Catalytic Behavior of the Nanoparticles Formed. In ACS Catalysis (Vol. 8, Issue 9, p. 8100-8106). https://doi.org/10.1021/acscatal.8b02338
(). Highly Selective and Sharp Volcano-type Synergistic Ni2 Pt@ZIF-8-Catalyzed Hydrogen Evolution from Ammonia Borane Hydrolysis. In Journal of the American Chemical Society (Vol. 140, Issue 31, p. 10034-10042). https://doi.org/10.1021/jacs.8b06511
(). Electron- and Hydride-Reservoir Organometallics as Precursors of Catalytically Efficient Transition Metal Nanoparticles in Water. In Chemistry - A European Journal (Vol. 24, Issue 25, p. 6645-6653). https://doi.org/10.1002/chem.201800418
(). Mechanistic and asymmetric investigations of the Au-catalysed cross-coupling between aryldiazonium salts and arylboronic acids using (P,N) gold complexes. In Chemical Communications (Vol. 54, Issue 91, p. 12867-12870). https://doi.org/10.1039/c8cc07530a
(). Highly hindered 2-(aryl-di-tert -butylsilyl)- N -methyl-imidazoles: A new tool for the aqueous 19F- and 18F-fluorination of biomolecule-based structures. In Chemical Communications (Vol. 54, Issue 40, p. 5098-5101). https://doi.org/10.1039/c8cc01782d
(). Synthesis of late transition-metal nanoparticles by Na naphthalenide reduction of salts and their catalytic efficiency. In Inorganic Chemistry Frontiers (Vol. 4, Issue 12, p. 2037-2044). https://doi.org/10.1039/c7qi00530j
(). Last-Step Pd-Mediated [11C]CO Labeling of a Moxestrol-Conjugated o-Iodobenzyl Alcohol: From Model Experiments to in Vivo Positron Emission Tomography Studies. In Bioconjugate Chemistry (Vol. 28, Issue 11, p. 2887-2894). https://doi.org/10.1021/acs.bioconjchem.7b00583
(). Bipyridyl– and pyridylquinolyl–phenothiazine structures as potential photoactive ligands: Syntheses and complexation to palladium. In Tetrahedron Letters (Vol. 58, Issue 32, p. 3096-3100). https://doi.org/10.1016/j.tetlet.2017.06.073
(). Exposure to air boosts CuAAC reactions catalyzed by PEG-stabilized Cu nanoparticles. In Chemical Communications (Vol. 53, Issue 39, p. 5384-5387). https://doi.org/10.1039/c7cc02504a
(). Gold-catalysed cross-coupling between aryldiazonium salts and arylboronic acids: Probing the usefulness of photoredox conditions. In Chemical Communications (Vol. 52, Issue 65, p. 10040-10043). https://doi.org/10.1039/c6cc04239b
(). From the gold-catalysed benzylation of arenes to the regio- and stereoselective synthesis of procyanidins dimers. In Tetrahedron (Vol. 71, Issue 20, p. 3045-3051). https://doi.org/10.1016/j.tet.2014.11.011
(). How wine polyphenols can fight Alzheimer disease progression: Towards a molecular explanation. In Tetrahedron (Vol. 71, Issue 20, p. 3163-3170). https://doi.org/10.1016/j.tet.2014.06.091
(). General last-step labeling of biomolecule-based substrates by [12C], [13C], and [11C] carbon monoxide. In Organic Letters (Vol. 17, Issue 2, p. 354-357). https://doi.org/10.1021/ol503471e
(). On the peculiar recycling properties of charcoal-supported palladium oxide nanoparticles in Sonogashira reactions. In Applied Catalysis A: General (Vol. 482, p. 157-162). https://doi.org/10.1016/j.apcata.2014.05.019
(). Palladium and copper-supported on charcoal: A heterogeneous multi-task catalyst for sequential Sonogashira-Click and Click-Heck reactions. In Journal of Organometallic Chemistry (Vol. 755, p. 78-85). https://doi.org/10.1016/j.jorganchem.2014.01.006
(). Heck-Matsuda arylation of olefins through a bicatalytic approach: Improved procedures and rationalization. In Advanced Synthesis and Catalysis (Vol. 356, Issue 5, p. 1065-1071). https://doi.org/10.1002/adsc.201301144
(). Isolation, characterization, and determination of a new compound in red wine. In Analytical and Bioanalytical Chemistry (Vol. 406, Issue 4, p. 1201-1208). https://doi.org/10.1007/s00216-013-7244-z
(). A new sif-dipropargyl glycerol scaffold as a versatile prosthetic group to design dimeric radioligands: Synthesis of the [18f]bmppsif tracer to image serotonin receptors. In ChemMedChem (Vol. 9, Issue 2, p. 337-349). https://doi.org/10.1002/cmdc.201300458
(). Pd0-catalyzed methyl transfer on nucleosides and oligonucleotides, envisaged as a PET tracer. In Molecules (Vol. 18, Issue 11, p. 13654-13665). https://doi.org/10.3390/molecules181113654
(). Stabilisation of carbon-supported palladium nanoparticles through the formation of an alloy with gold: Application to the Sonogashira reaction. In Chemistry - A European Journal (Vol. 19, Issue 42, p. 14024-14029). https://doi.org/10.1002/chem.201300347
(). Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst. In Beilstein Journal of Organic Chemistry (Vol. 9, p. 1426-1431). https://doi.org/10.3762/bjoc.9.160
(). Chelation-assisted cross-coupling of anilines through in situ activation as diazonium salts with boronic acids under ligand-, base-, and salt-free conditions. In Chemistry - A European Journal (Vol. 19, Issue 28, p. 9291-9296). https://doi.org/10.1002/chem.201300858
(). 11C click chemistry using [11C]methyl azide: Simplified, versatile, and practical alternative access to [11C] Nucleosides and [11C]oligonucleotides for PET imaging. In European Journal of Organic Chemistry (Issue 7, p. 1214-1217). https://doi.org/10.1002/ejoc.201201379
(). The colloidal state of tannins impacts the nature of their interaction with proteins: The case of salivary proline-rich protein/procyanidins binding. In Langmuir (Vol. 28, Issue 50, p. 17410-17418). https://doi.org/10.1021/la303964m
(). Sustainable heck-matsuda reaction with catalytic amounts of diazonium salts: An experimental and theoretical study. In Chemistry - A European Journal (Vol. 18, Issue 23, p. 7210-7218). https://doi.org/10.1002/chem.201200444
(). [ 18F]Si-RiboRGD: From design and synthesis to the imaging of α v β 3 integrins in melanoma tumors. In ChemPlusChem (Vol. 77, Issue 5, p. 345-349). https://doi.org/10.1002/cplu.201200022
(). Synthesis of indanones by sequential Heck-reduction-cyclization-alkylation (HRCA) reactions. In Tetrahedron Letters (Vol. 53, Issue 3, p. 338-341). https://doi.org/10.1016/j.tetlet.2011.11.042
(). Polyphenols and alzheimer’s disease: Tau/polyphenol interactions investigated by NMR and molecular modelling. In Nutrition and Aging (Vol. 1, Issue 3-4, p. 201-206). https://doi.org/10.3233/NUA-130015
(). A sustainable procedure combining the advantages of both homogeneous and heterogeneous catalysis for the heck-matsuda reaction. In Synthesis (Vol. 44, Issue 1, p. 37-41). https://doi.org/10.1055/s-0031-1289585
(). Unprecedented substoichiometric use of hazardous aryl diazonium salts in the Heck-Matsuda reaction via a double catalytic cycle. In Organic Letters (Vol. 13, Issue 10, p. 2646-2649). https://doi.org/10.1021/ol200752x
(). Recent advances in the Heck-Matsuda reaction in heterocyclic chemistry. In Tetrahedron (Vol. 67, Issue 16, p. 2815-2831). https://doi.org/10.1016/j.tet.2011.02.051
(). Silicon-based chemistry: An original and efficient one-step approach to [18F]-Nucleosides and [18F]-Oligonucleotides for PET imaging. In Chemistry - A European Journal (Vol. 17, Issue 11, p. 3096-3100). https://doi.org/10.1002/chem.201003234
(). A fully palladium-mediated construction of phenanthrenes and naphthoxindoles. In European Journal of Organic Chemistry (Issue 24, p. 4616-4622). https://doi.org/10.1002/ejoc.201100477
(). Aryl diazonium versus iodonium salts: Preparation, applications and mechanisms for the suzuki-miyaura cross-coupling reaction. In Advanced Synthesis and Catalysis (Vol. 353, Issue 17, p. 3063-3084). https://doi.org/10.1002/adsc.201100531
(). New strategies to study the chemical nature of wine oligomeric procyanidins. In Analytical and Bioanalytical Chemistry (Vol. 401, Issue 5, p. 1489-1499). https://doi.org/10.1007/s00216-011-4988-1
(). Towards a molecular interpretation of astringency: Synthesis, 3D structure, colloidal state, and human saliva protein recognition of procyanidins. In Planta Medica (Vol. 77, Issue 11, p. 1116-1122). https://doi.org/10.1055/s-0030-1270848
(). Reliable and safe, gram-scale hydrogenation and hydrogenolysis of O-benzyl ether groups with in situ Pd0/C catalyst. In Synthesis (Issue 18, p. 2893-2896). https://doi.org/10.1055/s-0030-1260167
(). A useful, reliable and safer protocol for hydrogenation and the hydrogenolysis of o-benzyl groups: The in situ preparation of an active Pd 0/C catalyst with well-defined properties. In Chemistry - A European Journal (Vol. 16, Issue 41, p. 12440-12445). https://doi.org/10.1002/chem.201001377
(). Room-temperature, ligand- and base-free heck reactions of aryl diazonium salts at low palladium loading: Sustainable preparation of substituted stilbene derivatives. In Chemistry - A European Journal (Vol. 16, Issue 17, p. 5191-5204). https://doi.org/10.1002/chem.200903050
(). Colloidal behavior of wine galloylated tannins. In Comptes Rendus Chimie (Vol. 13, Issue 5, p. 561-565). https://doi.org/10.1016/j.crci.2009.11.007
(). NMR of human saliva protein/wine tannin complexes. Towards deciphering astringency with physico-chemical tools. In Comptes Rendus Chimie (Vol. 13, Issue 4, p. 449-452). https://doi.org/10.1016/j.crci.2010.01.003
(). A 'click chemistry' approach to the efficient synthesis of modified nucleosides and oligonucleotides for PET imaging. In Tetrahedron Letters (Vol. 51, Issue 8, p. 1230-1232). https://doi.org/10.1016/j.tetlet.2009.12.120
(). Recyclable heterogeneous palladium catalysts in pure water: Sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. In Advanced Synthesis and Catalysis (Vol. 352, Issue 1, p. 33-79). https://doi.org/10.1002/adsc.200900765
(). NMR and molecular modeling of wine tannins binding to saliva proteins: Revisiting astringency from molecular and colloidal prospects. In FASEB Journal (Vol. 24, Issue 11, p. 4281-4290). https://doi.org/10.1096/fj.10-158741
(). A multi-task palladium catalyst involved in heck-reduction-cyclization sequences for the preparation of 4-benzyl-1,2-dihydroisoquinolin-3-ones: An unusual homogeneous-heterogeneous sustainable approach. In Synlett (Issue 10, p. 1539-1543). https://doi.org/10.1055/s-0029-1219926
(). Policosanol characterization and accumulation during ripening of Tunisian Olea europaea L. fruits. In European Journal of Lipid Science and Technology (Vol. 112, Issue 3, p. 373-379). https://doi.org/10.1002/ejlt.200900076
(). Heterogeneous palladium multi-task catalyst for sequential Heck-reduction-cyclization (HRC) reactions: influence of the support. In Tetrahedron Letters (Vol. 50, Issue 36, p. 5071-5074). https://doi.org/10.1016/j.tetlet.2009.06.084
(). Gas chromatographic-mass spectrometric characterisation of triterpene alcohols and monomethylsterols in developing Olea europaea L. fruits. In Food Chemistry (Vol. 116, Issue 1, p. 345-350). https://doi.org/10.1016/j.foodchem.2009.01.094
(). Preparation of 2-Quinolones by sequential heck reduction-cyclization (HRC) reactions by using a multitask palladium catalyst. In Chemistry - A European Journal (Vol. 15, Issue 29, p. 7238-7245). https://doi.org/10.1002/chem.200900583
(). Dynamic accumulation of 4-desmethylsterols and phytostanols during ripening of Tunisian Meski olives (Olea europea L.). In Food Chemistry (Vol. 112, Issue 4, p. 897-902). https://doi.org/10.1016/j.foodchem.2008.06.068
(). Synthesis of oxindoles by tandem heck-reduction-cyclization (HRC) from a single bifunctional, in situ generated Pd/C catalyst. In Journal of Organic Chemistry (Vol. 74, Issue 3, p. 1349-1352). https://doi.org/10.1021/jo802467s
(). Origin of brown discoloration in the staves of oak used in cooperage - Characterization of two new lignans in oak wood barrels. In Comptes Rendus Chimie (Vol. 12, Issue 1-2, p. 291-296). https://doi.org/10.1016/j.crci.2008.04.004
(). 3D-structure, colloidal behavior and Human saliva Protein recognition of wine tannins determined by NMR. In Acta Horticulturae (Vol. 841, p. 389-396). https://doi.org/10.17660/ActaHortic.2009.841.49
(). Improved Suzuki-Miyaura reactions of aryldiazonium salts with boronic acids by tuning palladium on charcoal catalyst properties. In Advanced Synthesis and Catalysis (Vol. 351, Issue 4, p. 649-655). https://doi.org/10.1002/adsc.200800783
(). Heck cross-coupling of aryldiazonium tetrafluoroborate with acrylates catalyzed by palladium on charcoal. In Advanced Synthesis and Catalysis (Vol. 350, Issue 16, p. 2559-2565). https://doi.org/10.1002/adsc.200800539
(). Modeling procyanidin self-association processes and understanding their micellar organization: A study by diffusion NMR and molecular mechanics. In Langmuir (Vol. 24, Issue 19, p. 11027-11035). https://doi.org/10.1021/la8015904
(). Heterogeneous multifunctional catalysts for tandem processes: An approach toward sustainability. In ChemSusChem (Vol. 1, Issue 8-9, p. 718-724). https://doi.org/10.1002/cssc.200800110
(). Structural diversity of nucleophilic adducts from flavanols and oak wood aldehydes. In Food Chemistry (Vol. 107, Issue 4, p. 1494-1505). https://doi.org/10.1016/j.foodchem.2007.10.012
(). Efficient and practical cross-coupling of arenediazonium tetrafluoroborate salts with boronic acids catalyzed by palladium(0)/barium carbonate. In Advanced Synthesis and Catalysis (Vol. 350, Issue 6, p. 863-868). https://doi.org/10.1002/adsc.200800025
(). Tetra- and monoorganotin reagents in palladium-mediated cross-coupling reactions for the labeling with carbon-11 of PET tracers. In Synthesis (Issue 6, p. 978-984). https://doi.org/10.1055/s-2008-1032206
(). Polyfunctional Tin Organometallics for Organic Synthesis. In Handbook of Functionalized Organometallics: Applications in Synthesis (Vol. 1, p. 203-249). https://doi.org/10.1002/9783527619467.ch6
(). State of art in 11C labelled radiotracers synthesis. In Current Medicinal Chemistry (Vol. 15, Issue 3, p. 235-277). https://doi.org/10.2174/092986708783497292
(). A kinetic study of the reactions of (+)-catechin with aldehydes derived from toasted oak. In Journal of the Science of Food and Agriculture (Vol. 87, Issue 11, p. 2081-2091). https://doi.org/10.1002/jsfa.2968
(). Structural and conformational analysis of two native procyanidin trimers. In Magnetic Resonance in Chemistry (Vol. 45, Issue 2, p. 157-166). https://doi.org/10.1002/mrc.1938
(). An improved synthesis of procyanidin dimers: Regio- and stereocontrol of the interflavan bond. In European Journal of Organic Chemistry (Issue 23, p. 5367-5377). https://doi.org/10.1002/ejoc.200600668
(). Structure of extracted lignins from oak heartwood (Quercus petraea Liebl., Q. Robur L.). In Comptes Rendus Chimie (Vol. 9, Issue 9, p. 1221-1233). https://doi.org/10.1016/j.crci.2006.02.005
(). A 3D structural and conformational study of procyanidin dimers in water and hydro-alcoholic media as viewed by NMR and molecular modeling. In Magnetic Resonance in Chemistry (Vol. 44, Issue 9, p. 868-880). https://doi.org/10.1002/mrc.1867
(). Pyrolysis-gas chromatography/mass spectrometry of Quercus sp. wood: Application to structural elucidation of macromolecules and aromatic profiles of different species. In Journal of Analytical and Applied Pyrolysis (Vol. 75, Issue 2, p. 181-193). https://doi.org/10.1016/j.jaap.2005.05.006
(). Methyl transfer reaction from monomethyltin reagent under palladium(0) catalysis: A versatile method for labelling with carbon-11. In Chemical Communications (Issue 1, p. 97-99). https://doi.org/10.1039/b510286c
(). Proanthocyanidins from Quercus petraea and Q. robur heartwood: Quantification and structures. In Comptes Rendus Chimie (Vol. 9, Issue 1 SPEC. ISS., p. 120-126). https://doi.org/10.1016/j.crci.2005.09.001
(). Development of direct size-exclusion chromatography separation for the determination of molar mass of native procyanidins in the phenolate form. In Journal of Chromatography A (Vol. 1089, Issue 1-2, p. 263-269). https://doi.org/10.1016/j.chroma.2005.07.002
(). Stille cross-coupling of activated alkyltin reagents under "ligandless" conditions. In Journal of Organic Chemistry (Vol. 70, Issue 5, p. 1953-1956). https://doi.org/10.1021/jo047907q
(). Global fractionation of oak heartwood extractable polymers (lignins, polysaccharides and ellagitannins) by selective precipitations. In Journal of the Science of Food and Agriculture (Vol. 85, Issue 3, p. 343-353). https://doi.org/10.1002/jsfa.1991
(). Three-dimensional structure and dynamics of wine tannin-saliva protein complexes. A multitechnique approach. In Biochemistry (Vol. 42, Issue 35, p. 10385-10395). https://doi.org/10.1021/bi034354p
(). Monoallylstannanes, reagents for allylic radical transfer. Part I. In Comptes Rendus de l'Academie des Sciences - Series IIc: Chemistry (Vol. 4, Issue 7, p. 641-648). https://doi.org/10.1016/S1387-1609(01)01287-7
(). A new carboxylic acid with branched ponytails for the solubilization of Mn(II) and Co(II) ions in perfluorocarbons. In Journal of Fluorine Chemistry (Vol. 108, Issue 2, p. 195-197). https://doi.org/10.1016/S0022-1139(01)00355-4
(). Observations on the versatility of methylenecyclopropanes as olefinic components in the intramolecular Pauson-Khand reaction. In Chemical Communications (Issue 2, p. 183-184). https://doi.org/10.1039/a807333c
(). The use of a monoorganotin derivative of pyrene in the palladium(0)-catalyzed synthesis of a new metal-cation complexing molecule displaying excited state charge transfer properties. In Tetrahedron Letters (Vol. 39, Issue 10, p. 1179-1182). https://doi.org/10.1016/S0040-4039(97)10811-5
(). NMR as a tool for kinetic studies: Application to the assessment of organotin reactivity. In Journal de Chimie Physique et de Physico-Chimie Biologique (Vol. 95, Issue 2, p. 377-383). https://doi.org/10.1051/jcp:1998147
(). Activated monoorganotins for the modified stille coupling reaction with triflates. In Synlett (Issue 12, p. 1323-1324). https://doi.org/10.1055/s-1998-1942
(). New monoorganostannanes as efficient reagents for palladium-Catalyzed coupling reactions. In Journal of Organic Chemistry (Vol. 62, Issue 16, p. 5242-5243). https://doi.org/10.1021/jo970465g
(). Halogen exchange in substituted allyltin halides studied by 2D NMR EXSY as a tool to assess reactivity. In Journal of Organometallic Chemistry (Vol. 524, Issue 1-2, p. 103-106). https://doi.org/10.1016/S0022-328X(96)06446-7
(). Observations on some Pd((0)) catalysed intermolecular reaction of electron deficient alkylidene cyclopropanes with olefins: A novel route to highly functionalised skipped diene units. In Tetrahedron Letters (Vol. 37, Issue 33, p. 5983-5986). https://doi.org/10.1016/0040-4039(96)01238-5
(). Some Intermolecular Pauson-Khand Reactions of Functionalised Alkylidenecyclopropanes. In Synlett (Vol. 1996, Issue 10, p. 990-992). https://doi.org/10.1055/s-1996-5645
(). Monoalkylstannanes as a new source of allyl radical transfer. In Journal of the Chemical Society, Chemical Communications (Issue 23, p. 2387-2388). https://doi.org/10.1039/C39950002387
(). 1,2-Addition of Tin Tetrachloride to Bicyclo[2.2.1]hepta-2,5-diene and 2,3-Benzobicyclo[2.2.1]hepta-2,5-diene. In Journal of Organic Chemistry (Vol. 59, Issue 26, p. 8292-8293). https://doi.org/10.1021/jo00105a061
(). Iminyl radicals: part II. ring opening of cyclobutyl- and cyclopentyliminyl radicals.. In Tetrahedron (Vol. 50, Issue 6, p. 1757-1768). https://doi.org/10.1016/S0040-4020(01)80850-4
(). Iminyl radicals: Part III. Further synthetically useful sources of iminyl radicals.. In Tetrahedron (Vol. 50, Issue 6, p. 1769-1776). https://doi.org/10.1016/S0040-4020(01)80851-6
(). Iminyl radicals: Part I. generation and intramolecular capture by an olefin.. In Tetrahedron (Vol. 50, Issue 6, p. 1745-1756). https://doi.org/10.1016/S0040-4020(01)80849-8
(). Study of halogen exchange in allyltin trihalides by two‐dimensional 119Sn EXSY NMR. In Magnetic Resonance in Chemistry (Vol. 32, Issue 10, p. 617-623). https://doi.org/10.1002/mrc.1260321010
(). Reactivity of functionalized allyltrihalostannanes: An easy entry to α-methylene-γ-lactones. In Tetrahedron Letters (Vol. 34, Issue 48, p. 7749-7752). https://doi.org/10.1016/S0040-4039(00)61555-1
(). A convenient synthesis of functionalized allyltrihalostannanes. In Journal of Organometallic Chemistry (Vol. 453, Issue 1). https://doi.org/10.1016/0022-328X(93)80343-A
(). Ring Opening Induced by Iminyl Radicals Derived from Cyclobutanones: New Aspects of Tin Hydride Cleavage of S-Phenyl Sulphenylimines. In Journal of the American Chemical Society (Vol. 113, Issue 3, p. 1055-1057). https://doi.org/10.1021/ja00003a057
(). A new and synthetically useful source of iminyl radicals.. In Tetrahedron Letters (Vol. 32, Issue 34, p. 4299-4302). https://doi.org/10.1016/S0040-4039(00)92153-1
(). Cyclisation of imine radicals derived from sulphenylimines: A simple access to Δ1-pyrrolines.. In Tetrahedron Letters (Vol. 31, Issue 1, p. 85-88). https://doi.org/10.1016/S0040-4039(00)94340-5
(). Multiple radical additions starting with iminyl radicals derived from sulphenylimines.. In Tetrahedron Letters (Vol. 31, Issue 25, p. 3545-3548). https://doi.org/10.1016/S0040-4039(00)94438-1
(). Nuclease activity of a water-soluble manganese porphyrin associated with potassium hydrogen persulphate: Oxidative cleavage of DNA. In Journal of the Chemical Society, Chemical Communications (Issue 15, p. 1169-1171). https://doi.org/10.1039/C39870001169