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Groupe de recherche
Synthèse organique et substances naturelles
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Enseignant-chercheur
Batiment
A12
Etage
RDC Ouest
Publications
(). Total Synthesis of (−)-Vescalagin, the Iconic Member of the C-Glucosidic Ellagitannin Family. In Chemistry A European Journal (Vol. 31, Issue 34, p. e202501159). https://doi.org/10.1002/chem.202501159
(). Heterogeneous Catalytic Oxidations with In Situ-Generated Hypervalent Iodine-Based Porous Organic Polymers. In Chemistry A European Journal (Vol. 31, Issue 18, p. e202403402). https://doi.org/10.1002/chem.202403402
(). ICP2023 - XXXI International Conference on Polyphenols (July 3-6, 2023, Nantes, France): “Under the Apple Tree”. In Journal of Agricultural and Food Chemistry (Vol. 73, Issue 9, p. 5005-5006). https://doi.org/10.1021/acs.jafc.5c00365
(). Copper(II)-Amine Complex-Mediated Intramolecular Coupling of Gallates: A Bioinspired Solution to the Atroposelective Synthesis of Ellagitannins. In Angewandte Chemie International Edition (Vol. 63, Issue 52, p. e202412036). https://doi.org/10.1002/anie.202412036
(). Total Synthesis of the Bacterial ortho-Quinol (+)-Strepantibin A through Iodyl-Type λ5-Iodane-Promoted Asymmetric Hydroxylative Phenol Dearomatization. In Organic Letters (Vol. 26, Issue 29, p. 6086-6091). https://doi.org/10.1021/acs.orglett.4c01653
(). Synthesis of obovatol and related neolignan analogues as α-glucosidase and α-amylase inhibitors. In Bioorganic Chemistry (Vol. 147, p. 107392). https://doi.org/10.1016/j.bioorg.2024.107392
(). Systemic Convergent Multitarget Interactions of Plant Polyphenols Revealed by Affinity-Based Protein Profiling of Bone Cells Using C-Glucosidic Vescal(ag)in-Bearing Chemoproteomic Probes. In ACS Chemical Biology (Vol. 18, Issue 12, p. 2495-2505). https://doi.org/10.1021/acschembio.3c00440
(). Asymmetric Allenylation of Alkynes mediated by Chiral Organoselenated Reagents under Oxidative Conditions. In Angewandte Chemie International Edition (Vol. 62, Issue 42, p. e202310436). https://doi.org/10.1002/anie.202310436
(). Fast and precise chiroptical spectroscopy by photoelectron elliptical dichroism. In Physical Chemistry Chemical Physics (Vol. 25, Issue 24, p. 16246-16263). https://doi.org/10.1039/d3cp01057k
(). Synthesis of Flavonol-Bearing Probes for Chemoproteomic and Bioinformatic Analyses of Asteraceae Petals in Search of Novel Flavonoid Enzymes. In International Journal of Molecular Sciences (Vol. 24, Issue 11, p. 9724). https://doi.org/10.3390/ijms24119724
(). ortho-Quinols in (Bio)Synthesis of Natural Products. In European Journal of Organic Chemistry (Vol. 26, Issue 13, p. e202201224). https://doi.org/10.1002/ejoc.202201224
(). Effect of castalagin against HSV-1 infection in newborn mice. In Natural Product Research (Vol. 37, Issue 24, p. 4156-4161). https://doi.org/10.1080/14786419.2023.2173191
(). Preparation of a ε-caprolactonic diterpenoid derivate by unexpected oxidative cleavage/lactonization of 2-oxoaustroeupatol. In Natural Products and Bioprospecting (Vol. 12, Issue 1, p. 20). https://doi.org/10.1007/s13659-022-00343-2
(). Novel 7-Chloro-(4-thioalkylquinoline) Derivatives: Synthesis and Antiproliferative Activity through Inducing Apoptosis and DNA/RNA Damage. In Pharmaceuticals (Vol. 15, Issue 10, p. 1234). https://doi.org/10.3390/ph15101234
(). Identification, quantitation and sensory contribution of new C-glucosidic ellagitannin-derived spirit compounds. In Food Chemistry (Vol. 384, p. 132307). https://doi.org/10.1016/j.foodchem.2022.132307
(). Isolation of a new taste-active brandy tannin A: Structural elucidation, quantitation and sensory assessment. In Food Chemistry (Vol. 377, p. 131963). https://doi.org/10.1016/j.foodchem.2021.131963
(). Bispericyclic Diels–Alder Dimerization of ortho-Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6-Step Synthesis of (+)-Maytenone. In Angewandte Chemie International Edition (Vol. 60, Issue 27, p. 14967-14974). https://doi.org/10.1002/anie.202103410
(). Real-Time Analysis of Polyphenol–Protein Interactions by Surface Plasmon Resonance Using Surface-Bound Polyphenols. In Chemistry A European Journal (Vol. 27, Issue 17, p. 5498-5508). https://doi.org/10.1002/chem.202005187
(). Antiviral properties of the nsaid drug naproxen targeting the nucleoprotein of sars-cov-2 coronavirus. In Molecules (Vol. 26, Issue 9, p. 2593). https://doi.org/10.3390/molecules26092593
(). Maternal alcoholism and neonatal hypoxia-ischemia: Neuroprotection by stilbenoid polyphenols. In Brain Research (Vol. 1738, p. 146798). https://doi.org/10.1016/j.brainres.2020.146798
(). C-glucosidic ellagitannins and galloylated glucoses as potential functional food ingredients with anti-diabetic properties: a study of α-glucosidase and α-amylase inhibition. In Food Chemistry (Vol. 313, p. 126099). https://doi.org/10.1016/j.foodchem.2019.126099
(). Synthesis and Biological Evaluation of Hapten-Clicked Analogues of The Antigenic Peptide Melan-A/MART-126(27L)-35. In Chemmedchem (Vol. 15, Issue 9, p. 799-807). https://doi.org/10.1002/cmdc.202000038
(). Synthesis and leishmanicidal evaluation of sulfanyl- and sulfonyl-tethered functionalized benzoate derivatives featuring a nitroimidazole moiety. In Archiv Der Pharmazie (Vol. 353, Issue 5, p. e2000002). https://doi.org/10.1002/ardp.202000002
(). Impact of polyphenols on receptor–ligand interactions by NMR: the case of neurotensin (NT)–neurotensin receptor fragment (NTS1) complex. In Journal of Biomolecular Structure and Dynamics (Vol. 38, Issue 5, p. 1467-1478). https://doi.org/10.1080/07391102.2019.1608863
(). Blue LED Irradiation of Iodonium Ylides Gives Diradical Intermediates for Efficient Metal-free Cyclopropanation with Alkenes. In Angewandte Chemie International Edition (Vol. 58, Issue 47, p. 16959-16965). https://doi.org/10.1002/anie.201908994
(). Bio-inspired Total Synthesis of Twelve Securinega Alkaloids: Structural Reassignments of (+)-Virosine B and (−)-Episecurinol A. In Chemistry A European Journal (Vol. 25, Issue 49, p. 11574-11580). https://doi.org/10.1002/chem.201903122
(). Interaction between Ellagitannins and Salivary Proline-Rich Proteins. In Journal of Agricultural and Food Chemistry (Vol. 67, Issue 34, p. 9579-9590). https://doi.org/10.1021/acs.jafc.9b02574
(). Ellagitannins and flavano-ellagitannins: Red wines tendency in different areas, barrel origin and ageing time in barrel and bottle. In Biomolecules (Vol. 9, Issue 8, p. 316). https://doi.org/10.3390/biom9080316
(). Hemisynthesis and Bactericidal Activity of Several Substituted Benzoic Acid Esters of 13(S)-Labdan-8α,15-Diol, a Diterpene from Oxylobus glanduliferus. In Chemistry of Natural Compounds (Vol. 55, Issue 4, p. 677-684). https://doi.org/10.1007/s10600-019-02777-6
(). Synthesis of [7]Helicene Enantiomers and Exploratory Study of Their Conversion into Helically Chiral Iodoarenes and Iodanes. In Chemistry A European Journal (Vol. 25, Issue 11, p. 2852-2858). https://doi.org/10.1002/chem.201805761
(). Reactivity of wine polyphenols under oxidation conditions: Hemisynthesis of adducts between grape catechins or oak ellagitannins and odoriferous thiols. In Tetrahedron (Vol. 75, Issue 5, p. 551-560). https://doi.org/10.1016/j.tet.2018.11.071
(). Preparation and bactericidal activity of oxidation derivatives of austroeupatol, an ent-nor-furano diterpenoid of the labdane series from Austroeupatorium inulifolium. In Phytochemistry Letters (Vol. 29, p. 47-52). https://doi.org/10.1016/j.phytol.2018.11.007
(). Recent Advances in Polyphenol Research. In Recent Advances in Polyphenol Research (Vol. 6, p. 1-403). https://doi.org/10.1002/9781119427896
(). Anti-Herpes Simplex Virus Type 1 Activity of Specially Selected Groups of Tannins. In Drug Research (Vol. 69, Issue 7, p. 374-381). https://doi.org/10.1055/a-0640-2557
(). Rapid Screening of Ellagitannins in Natural Sources via Targeted Reporter Ion Triggered Tandem Mass Spectrometry. In Scientific Reports (Vol. 8, Issue 1, p. 10399). https://doi.org/10.1038/s41598-018-27708-3
(). Anti-osteoclastic effects of C-glucosidic ellagitannins mediated by actin perturbation. In European Journal of Cell Biology (Vol. 97, Issue 8, p. 533-545). https://doi.org/10.1016/j.ejcb.2018.09.003
(). Two new oleanane-type saponins from hydrocotyle multifida. In Natural Product Communications (Vol. 13, Issue 11, p. 1453-1456). https://doi.org/10.1177/1934578x1801301110
(). From Naproxen Repurposing to Naproxen Analogues and Their Antiviral Activity against Influenza A Virus. In Journal of Medicinal Chemistry (Vol. 61, Issue 16, p. 7202-7217). https://doi.org/10.1021/acs.jmedchem.8b00557
(). Synthesis of Scyphostatin Analogues through Hypervalent Iodine-Mediated Phenol Dearomatization. In Journal of Organic Chemistry (Vol. 82, Issue 22, p. 11816-11828). https://doi.org/10.1021/acs.joc.7b02366
(). Bioinspired Total Synthesis of (−)-Vescalin: A Nonahydroxytriphenoylated C-Glucosidic Ellagitannin. In Angewandte Chemie International Edition (Vol. 56, Issue 44, p. 13833-13837). https://doi.org/10.1002/anie.201707613
(). Asymmetric Alkynylation of β-Ketoesters and Naphthols Promoted by New Chiral Biphenylic Iodanes. In Chemistry A European Journal (Vol. 23, Issue 54, p. 13309-13313). https://doi.org/10.1002/chem.201703238
(). Triterpene saponins from Billia rosea. In Phytochemistry (Vol. 141, p. 105-113). https://doi.org/10.1016/j.phytochem.2017.04.023
(). Oleanane-type glycosides from Pittosporum tenuifolium “variegatum” and P. tenuifolium “gold star”. In Phytochemistry (Vol. 140, p. 166-173). https://doi.org/10.1016/j.phytochem.2017.04.013
(). Ortho-Quinol Acetate Chemistry: Reactivity toward Aryl-Based Nucleophiles and Applications to the Synthesis of Natural Products. In Journal of Organic Chemistry (Vol. 82, Issue 7, p. 3990-3995). https://doi.org/10.1021/acs.joc.7b00250
(). Asymmetric dearomative spirolactonization of naphthols using λ3-iodanes under chiral phase-transfer catalysis. In Tetrahedron (Vol. 73, Issue 26, p. 3684-3690). https://doi.org/10.1016/j.tet.2017.04.028
(). Preface. In Recent Advances in Polyphenol Research (Vol. 5, p. xix-xxi). https://doi.org/10.1002/9781118883303
(). Phenol dearomatization with hypervalent iodine reagents. In Topics in Current Chemistry (Vol. 373, p. 25-74). https://doi.org/10.1007/128_2015_665
(). Immobilization of flavan-3-ols onto sensor chips to study their interactions with proteins and pectins by SPR. In Applied Surface Science (Vol. 371, p. 512-518). https://doi.org/10.1016/j.apsusc.2016.03.002
(). Biological activity of ellagitannins: Effects as anti-oxidants, pro-oxidants and metal chelators. In Phytochemistry (Vol. 125, p. 65-72). https://doi.org/10.1016/j.phytochem.2016.02.008
(). Total Synthesis of (-)-Bacchopetiolone via an Asymmetric Hydroxylative Phenol Dearomatization/[4+2]-Dimerization Cascade Promoted by a Novel Salen-Type Chiral Iodane. In Organic Letters (Vol. 18, Issue 5, p. 1120-1123). https://doi.org/10.1021/acs.orglett.6b00224
(). Structure-based design of novel naproxen derivatives targeting monomeric nucleoprotein of Influenza A virus. In Journal of Biomolecular Structure and Dynamics (Vol. 33, Issue 9, p. 1899-1912). https://doi.org/10.1080/07391102.2014.979230
(). Gallotannins and Tannic Acid: First Chemical Syntheses and in Vitro Inhibitory Activity on Alzheimer's Amyloid β-Peptide Aggregation. In Angewandte Chemie International Edition (Vol. 54, Issue 28, p. 8217-8221). https://doi.org/10.1002/anie.201411606
(). About the impact of oak ellagitannins on wine odoriferous thiols under acidic and oxidation conditions. In Tetrahedron (Vol. 71, Issue 20, p. 2991-2998). https://doi.org/10.1016/j.tet.2015.02.036
(). Chemistry in the vine and wine sciences. In Tetrahedron (Vol. 71, Issue 20, p. 2969-2970). https://doi.org/10.1016/j.tet.2015.02.086
(). Polyphenolic C-glucosidic ellagitannins present in oak-aged wine inhibit HIV-1 nucleocapsid protein. In Tetrahedron (Vol. 71, Issue 20, p. 3020-3026). https://doi.org/10.1016/j.tet.2015.01.035
(). Chemical composition of the essential oil of gynoxys meridana from mérida, Venezuela. In Natural Product Communications (Vol. 10, Issue 4, p. 653-654). https://doi.org/10.1177/1934578x1501000431
(). Asymmetric hydroxylative phenol dearomatization promoted by chiral binaphthylic and biphenylic iodanes. In Angewandte Chemie International Edition (Vol. 53, Issue 37, p. 9860-9864). https://doi.org/10.1002/anie.201403571
(). Recent Advances in Polyphenol Research. In Recent Advances in Polyphenol Research (Vol. 4, p. 1-437). https://doi.org/10.1002/9781118329634
(). New affinity-based probes for capturing flavonoid-binding proteins. In Chemical Communications (Vol. 50, Issue 67, p. 9387-9389). https://doi.org/10.1039/c4cc04557b
(). Facile and sustainable synthesis of the natural antioxidant hydroxytyrosol. In Tetrahedron Letters (Vol. 55, Issue 15, p. 2455-2458). https://doi.org/10.1016/j.tetlet.2014.02.134
(). Acylated oleanane-type saponins from Ganophyllum giganteum. In Phytochemistry (Vol. 98, p. 236-242). https://doi.org/10.1016/j.phytochem.2013.11.003
(). Protecting-group-free solid-phase anchoring of polyphenolic C-glucosidic ellagitannins and synthesis of 1-alkylamino-vescalagin derivatives. In European Journal of Organic Chemistry (Vol. 2014, Issue 23, p. 4963-4972). https://doi.org/10.1002/ejoc.201402444
(). Ellagitannins as synergists of ACV on the replication of ACV-resistant strains of HSV 1 and 2. In Antiviral Research (Vol. 110, p. 104-114). https://doi.org/10.1016/j.antiviral.2014.07.017
(). Oxidative Coupling of Phenols and Phenol Ethers. In Comprehensive Organic Synthesis Second Edition (Vol. 3, p. 656-740). https://doi.org/10.1016/B978-0-08-097742-3.00318-9
(). Hemisynthesis and structural and chromatic characterization of delphinidin 3- O -glucoside-vescalagin hybrid pigments. In Journal of Agricultural and Food Chemistry (Vol. 61, Issue 47, p. 11560-11568). https://doi.org/10.1021/jf4033188
(). Thermodynamic and kinetic properties of a new myrtillin-vescalagin hybrid pigment. In Journal of Agricultural and Food Chemistry (Vol. 61, Issue 47, p. 11569-11578). https://doi.org/10.1021/jf403319u
(). Remarkable biomimetic chemoselective aerobic oxidation of flavano-ellagitannins found in oak-aged wine. In Angewandte Chemie International Edition (Vol. 52, Issue 44, p. 11530-11533). https://doi.org/10.1002/anie.201305839
(). Steroidal saponins from the fruits of Solanum torvum. In Phytochemistry (Vol. 86, p. 137-143). https://doi.org/10.1016/j.phytochem.2012.10.010
(). Hydrolyzable tannins: Gallotannins and ellagitannins. In Natural Products Phytochemistry Botany and Metabolism of Alkaloids Phenolics and Terpenes (p. 1975-2010). https://doi.org/10.1007/978-3-642-22144-6_65
(). Synthetic studies toward c-glucosidic ellagitannins: A biomimetic total synthesis of 5-O-desgalloylepipunicacortein A. In Chemistry A European Journal (Vol. 18, Issue 29, p. 9063-9074). https://doi.org/10.1002/chem.201200517
(). Resveratrol still has something to say about aging!. In Angewandte Chemie International Edition (Vol. 51, Issue 28, p. 6824-6826). https://doi.org/10.1002/anie.201203059
(). The polyphenolic ellagitannin vescalagin acts as a preferential catalytic inhibitor of the α isoform of human DNA topoisomerase II. In Molecular Pharmacology (Vol. 82, Issue 1, p. 134-141). https://doi.org/10.1124/mol.111.077537
(). Identification of adducts between an odoriferous volatile thiol and oxidized grape phenolic compounds: Kinetic study of adduct formation under chemical and enzymatic oxidation conditions. In Journal of Agricultural and Food Chemistry (Vol. 60, Issue 10, p. 2647-2656). https://doi.org/10.1021/jf204295s
(). Recent Advances in Polyphenol Research. In Recent Advances in Polyphenol Research (Vol. 3). https://doi.org/10.1002/9781118299753
(). Hydrolyzable tannins: Gallotannins, ellagitannins, and ellagic acid. In Handbook of Analysis of Active Compounds in Functional Foods (p. 435-459). https://doi.org/10.1201/b11653
(). Synthesis of Biologically Active Catecholic Compounds via ortho-Selective Oxygenation of Phenolic Compounds Using Hypervalent Iodine(V) Reagents. In Current Organic Synthesis (Vol. 9, Issue 5, p. 650-669). https://doi.org/10.2174/157017912803251792
(). Steroidal Saponins from the Fruits of Cestrum ruizteranianum. In Natural Product Communications (Vol. 6, Issue 12). https://doi.org/10.1177/1934578X1100601209
(). Triumph for unnatural synthesis. In Nature (Vol. 474, Issue 7352, p. 459-460). https://doi.org/10.1038/474459a
(). Binding of filamentous actin and winding into fibrillar aggregates by the polyphenolic C-glucosidic ellagitannin vescalagin. In Angewandte Chemie International Edition (Vol. 50, Issue 22, p. 5099-5104). https://doi.org/10.1002/anie.201006712
(). First and biomimetic total synthesis of a member of the C-glucosidic subclass of ellagitannins, 5-O-desgalloylepipunicacortein A. In Chemical Communications (Vol. 47, Issue 5, p. 1628-1630). https://doi.org/10.1039/c0cc04007j
(). Three-dimensional analysis of combination effect of ellagitannins and acyclovir on herpes simplex virus types 1 and 2. In Antiviral Research (Vol. 89, Issue 2, p. 174-181). https://doi.org/10.1016/j.antiviral.2010.11.014
(). Plant polyphenols: Chemical properties, biological activities, and synthesis. In Angewandte Chemie International Edition (Vol. 50, Issue 3, p. 586-621). https://doi.org/10.1002/anie.201000044
(). Identification, amounts, and kinetics of extraction of C-glucosidic ellagitannins during wine aging in oak barrels or in stainless steel tanks with oak chips. In Analytical and Bioanalytical Chemistry (Vol. 401, Issue 5, p. 1535-1543). https://doi.org/10.1007/s00216-011-4949-8
(). New triterpenoid and ergostane glycosides from the leaves of Hydrocotyle umbellata L.. In Helvetica Chimica Acta (Vol. 94, Issue 10, p. 1850-1859). https://doi.org/10.1002/hlca.201100109
(). Development of an Affinity-Based Proteomic Strategy for the Elucidation of Proanthocyanidin Biosynthesis. In Chembiochem (Vol. 12, Issue 8, p. 1193-1197). https://doi.org/10.1002/cbic.201100044
(). Synthesis of ellagitannin natural products. In Natural Product Reports (Vol. 28, Issue 5, p. 853-874). https://doi.org/10.1039/c0np00058b
(). Design, synthesis and evaluation of β-lactam antigenic peptide hybrids; Unusual opening of the β-lactam ring in acidic media. In Organic and Biomolecular Chemistry (Vol. 8, Issue 23, p. 5345-5353). https://doi.org/10.1039/c003877f
(). Crystal structures of HLA-A*0201 complexed with melan-A/MART-1 26(27L)-35 peptidomimetics reveal conformational heterogeneity and highlight degeneracy of T cell recognition. In Journal of Medicinal Chemistry (Vol. 53, Issue 19, p. 7061-7066). https://doi.org/10.1021/jm100683p
(). Hypervalent iodine chemistry - Recent advances and applications. In Tetrahedron (Vol. 66, Issue 31, p. 5737-5738). https://doi.org/10.1016/j.tet.2010.06.026
(). Hypervalent iodine-mediated oxygenative phenol dearomatization reactions. In Tetrahedron (Vol. 66, Issue 31, p. 5908-5917). https://doi.org/10.1016/j.tet.2010.05.078
(). Triterpene Saponins from the Fruits of Phytolacca rugosa (Phytolaccaceae). In Natural Product Communications (Vol. 5, Issue 5). https://doi.org/10.1177/1934578X1000500519
(). Ellagitannins - An Underestimated Class of Plant Polyphenols: Chemical Reactivity of C-Glucosidic Ellagitannins in Relation to Wine Chemistry and Biological Activity. In Recent Advances in Polyphenol Research (Vol. 2, p. 81-137). https://doi.org/10.1002/9781444323375.ch4
(). Hypervalent iodine-mediated phenol dearomatization in natural product synthesis. In Tetrahedron (Vol. 66, Issue 13, p. 2235-2261). https://doi.org/10.1016/j.tet.2009.12.046
(). Evaluating the potential of chestnut (Castanea sativa Mill.) fruit pericarp and integument as a source of tocopherols, pigments and polyphenols. In Industrial Crops and Products (Vol. 31, Issue 2, p. 301-311). https://doi.org/10.1016/j.indcrop.2009.11.008
(). Physicochemical studies of new anthocyano-ellagitannin hybrid pigments: About the origin of the influence of oak C-glycosidic ellagitannins on wine color. In European Journal of Organic Chemistry (Issue 1, p. 55-63). https://doi.org/10.1002/ejoc.200901133
(). New steroidal alkaloids from Solanum hypomalacophyllum. In Natural Product Communications (Vol. 5, Issue 11, p. 1743-1746). https://doi.org/10.1177/1934578x1000501108
(). Stable solid-supported leucoanthocyanidin variants for flavanoid biosynthesis elucidation. In Tetrahedron Letters (Vol. 50, Issue 47, p. 6567-6571). https://doi.org/10.1016/j.tetlet.2009.09.045
(). Specific or nonspecific protein-polyphenol interactions? Discrimination in real time by surface plasmon resonance. In Chembiochem (Vol. 10, Issue 14, p. 2321-2324). https://doi.org/10.1002/cbic.200900287
(). Asymmetrie hydroxylative phenol dearomatization through in situ generation of iodanes from chiral iodoarenes and m-CPBA. In Angewandte Chemie International Edition (Vol. 48, Issue 25, p. 4605-4609). https://doi.org/10.1002/anie.200901039
(). Chemistry and biology of ellagitannins: An underestimated class of bioactive plant polyphenols. In Chemistry and Biology of Ellagitannins an Underestimated Class of Bioactive Plant Polyphenols (p. 1-374). https://doi.org/10.1142/6795
(). C-glycosidic ellagitannins and their influence on wine chemistry. In Chemistry and Biology of Ellagitannins an Underestimated Class of Bioactive Plant Polyphenols (p. 320-366). https://doi.org/10.1142/9789812797414_0009
(). Highly diastereoselective synthesis of orthoquinone monoketals through λ13-iodane-mediated oxidative dearomatization of phenols. In Angewandte Chemie International Edition (Vol. 47, Issue 19, p. 3552-3555). https://doi.org/10.1002/anie.200705816
(). Oxidative dearomatization of phenols: Why, how and what for?. In Synlett (Issue 4, p. 467-495). https://doi.org/10.1055/s-2008-1032094
(). Total synthesis of wasabidienones B1 and B0 via SIBX-mediated hydroxylative phenol dearomatization. In Organic Letters (Vol. 10, Issue 22, p. 5211-5214). https://doi.org/10.1021/ol802183p
(). Total synthesis of (+)-aquaticol by biomimetic phenol dearomatization: Double diastereofacial differentiation in the Diels-Alder dimerization of orthoquinols with a C2-symmetric transition state (Angewandte Chemie - International Edition (2007) 46, (1533-1535)). In Angewandte Chemie International Edition (Vol. 47, Issue 4, p. 628). https://doi.org/10.1002/anie.200890007
(). Plant Phenolics - Secondary Metabolites with Diverse Functions. In Recent Advances in Polyphenol Research (Vol. 1, p. 1-35). https://doi.org/10.1002/9781444302400.ch1
(). Regio- and stereoselectivities in Diels-Alder cyclodimerizations of orthoquinonoid cyclohexa-2,4-dienones. In Tetrahedron (Vol. 63, Issue 28, p. 6493-6505). https://doi.org/10.1016/j.tet.2007.03.035
(). Inhibition of topoisomerase I cleavage activity by thiol-reactive compounds: Importance of vicinal cysteines 504 and 505. In Journal of Biological Chemistry (Vol. 282, Issue 19, p. 14403-14412). https://doi.org/10.1074/jbc.M611673200
(). Synthetic anticancer vaccine candidates: Rational design of antigenic peptide mimetics that activate tumor-specific T-cells. In Journal of Medicinal Chemistry (Vol. 50, Issue 7, p. 1598-1609). https://doi.org/10.1021/jm0613368
(). UV light impact on ellagitannins and wood surface colour of European oak (Quercus petraea and Quercus robur). In Applied Surface Science (Vol. 253, Issue 11, p. 4985-4989). https://doi.org/10.1016/j.apsusc.2006.11.005
(). Total synthesis of (+)-aquaticol by biomimetic phenol dearomatization: Double diastereofacial differentiation in the Diels-Alder dimerization of orthoquinols with a C2-symmetric transition state. In Angewandte Chemie International Edition (Vol. 46, Issue 9, p. 1533-1535). https://doi.org/10.1002/anie.200604610
(). Efficient access to orthoquinols and their [4 + 2] cyclodimers via SIBX-mediated hydroxylative phenol dearomatization. In Journal of Organic Chemistry (Vol. 72, Issue 16, p. 6280-6283). https://doi.org/10.1021/jo0708893
(). Extraction, detection, and quantification of flavano-ellagitannins and ethylvescalagin in a Bordeaux red wine aged in oak barrels. In Journal of Agricultural and Food Chemistry (Vol. 54, Issue 19, p. 7349-7354). https://doi.org/10.1021/jf061724i
(). Safe oxidation of sulfides into sulfoxides using SIBX. In Tetrahedron Letters (Vol. 47, Issue 33, p. 5869-5873). https://doi.org/10.1016/j.tetlet.2006.06.072
(). Recognition characters in peptide-polyphenol complex formation. In Biochimica Et Biophysica Acta General Subjects (Vol. 1760, Issue 6, p. 951-958). https://doi.org/10.1016/j.bbagen.2006.01.005
(). Covalent modification of a melanoma-derived antigenic peptide with a natural quinone methide. Preliminary chemical, molecular modelling and immunological evaluation studies. In Molecular Biosystems (Vol. 2, Issue 5, p. 240-249). https://doi.org/10.1039/b518044a
(). Colorimetric evaluation of phenolic content and GC-MS characterization of phenolic composition of alimentary and cosmetic argan oil and press cake. In Journal of Agricultural and Food Chemistry (Vol. 53, Issue 23, p. 9122-9127). https://doi.org/10.1021/jf051082j
(). The chemistry of wine polyphenolic C-glycosidic ellagitannins targeting human topoisomerase II. In Chemistry A European Journal (Vol. 11, Issue 22, p. 6503-6513). https://doi.org/10.1002/chem.200500428
(). Regioselective hypervalent-iodine(III)-mediated dearomatizing phenylation of phenols through direct ligand coupling. In Angewandte Chemie International Edition (Vol. 44, Issue 43, p. 7065-7069). https://doi.org/10.1002/anie.200501638
(). Evaluation of selected South African medicinal plants for inhibitory properties against human immunodeficiency virus type 1 reverse transcriptase and integrase. In Journal of Ethnopharmacology (Vol. 99, Issue 1, p. 83-91). https://doi.org/10.1016/j.jep.2005.01.056
(). λ3-Iodane-mediated arenol dearomatization. Synthesis of five-membered ring-containing analogues of the aquayamycin ABC tricyclic unit and novel access to the apoptosis inducer menadione. In Tetrahedron (Vol. 61, Issue 6, p. 1551-1562). https://doi.org/10.1016/j.tet.2004.11.072
(). Oxidative dearomatization of phenols and anilines via λ3 - and λ5-iodane-mediated phenylation and oxygenation. In Molecules (Vol. 10, Issue 1, p. 201-216). https://doi.org/10.3390/10010201
(). Electrochemical synthesis of dimerizing and nondimerizing orthoquinone monoketals. In Journal of Organic Chemistry (Vol. 69, Issue 25, p. 8731-8738). https://doi.org/10.1021/jo048677i
(). Main structural and stereochemical aspects of the antiherpetic activity of nonahydroxyterphenoyl-containing C-glycosidic ellagitannins. In Chemistry and Biodiversity (Vol. 1, Issue 2, p. 247-258). https://doi.org/10.1002/cbdv.200490021
(). First asymmetric synthesis of orthoquinone monoketal enantiomers via anodic oxidation. In Organic Letters (Vol. 6, Issue 24, p. 4571-4573). https://doi.org/10.1021/ol048030k
(). Plant "polyphenolic" small molecules can induce a calorie restriction-mimetic life-span extension by activating sirtuins: Will "polyphenols" someday be used as chemotherapeutic drugs in western medicine?. In Chembiochem (Vol. 5, Issue 4, p. 427-430). https://doi.org/10.1002/cbic.200300835
(). Oxidative Conversion of Arenols into ortho-Quinols and ortho-Quinone Monoketals – A Useful Tactic in Organic Synthesis. In Modern Arene Chemistry (p. 539-573). https://doi.org/10.1002/3527601767.ch15
(). Chemical and electrochemical oxidative activation of arenol derivatives for carbon-carbon bond formation. In Current Organic Chemistry (Vol. 8, Issue 2, p. 113-148). https://doi.org/10.2174/1385272043486016
(). DNA Topoisomerase Inhibitor Acutissimin A and Other Flavano-Ellagitannins in Red Wine. In Angewandte Chemie International Edition (Vol. 42, Issue 48, p. 6012-6014). https://doi.org/10.1002/anie.200352089
(). Complex C-glycosyl flavonoid phytoalexins from Cucumis sativus. In Journal of Natural Products (Vol. 66, Issue 9, p. 1280-1283). https://doi.org/10.1021/np030150y
(). A stabilized formulation of IBX (SIBX) for safe oxidation reactions including a new oxidative demethylation of phenolic methyl aryl ethers. In Organic Letters (Vol. 5, Issue 16, p. 2903-2906). https://doi.org/10.1021/ol0349965
(). Enantiospecific Synthesis of the Antituberculosis Marine Sponge Metabolite (+)-Puupehenone. The Arenol Oxidative Activation Route. In Organic Letters (Vol. 4, Issue 22, p. 3975-3978). https://doi.org/10.1021/ol026855t
(). Extractives content in cooperage oak wood during natural seasoning and toasting; influence of tree species, geographic location, and single-tree effects. In Journal of Agricultural and Food Chemistry (Vol. 50, Issue 21, p. 5955-5961). https://doi.org/10.1021/jf020494e
(). A convenient synthesis of the Echinacea-derived immunostimulator and HIV-1 integrase inhibitor (-)-(2R,3R)-chicoric acid. In Helvetica Chimica Acta (Vol. 85, Issue 8, p. 2328-2334). https://doi.org/10.1002/1522-2675(200208)85:8<2328::AID-HLCA2328>3.0.CO;2-X
(). Electrochemically-induced spirolactonization of α-(methoxyphenoxy)alkanoic acids into quinone ketals. In Journal of Organic Chemistry (Vol. 67, Issue 13, p. 4458-4465). https://doi.org/10.1021/jo020023r
(). Iodine (III)-mediated generation of nitrogen-tethered orthoquinol acetates for the construction of oxygenated indole, quinoline, and phenanthridine alkaloid motifs. In Journal of Organic Chemistry (Vol. 67, Issue 10, p. 3425-3436). https://doi.org/10.1021/jo020010d
(). Hypervalent iodine(III)-mediated oxidative acetoxylation of 2-methoxyphenols for regiocontrolled nitrogen benzannulation. In Tetrahedron Letters (Vol. 42, Issue 42, p. 7393-7396). https://doi.org/10.1016/S0040-4039(01)01514-3
(). Oxidative activation of aromatic rings: An efficient strategy for arene functionalization. In Tetrahedron (Vol. 57, Issue 2, p. ix-x). https://doi.org/10.1016/S0040-4020(00)00933-9
(). 2-Alkoxyarenol-derived orthoquinols in carbon-oxygen, carbon-nitrogen and carbon-carbon bond-forming reactions. In Tetrahedron (Vol. 57, Issue 2, p. 319-329). https://doi.org/10.1016/S0040-4020(00)00939-X
(). Identification of the lipophilic factor produced by macrophages that stimulates steroidogenesis. In Endocrinology (Vol. 141, Issue 3, p. 953-958). https://doi.org/10.1210/endo.141.3.7350
(). Oxidized arenol intermediates in intermolecular carbon-carbon bond formation. Naphthoid cyclohexa-2,4-dienones via oxidative nucleophilic substitution. In Organic Letters (Vol. 1, Issue 10, p. 1651-1654). https://doi.org/10.1021/ol9910363
(). Orthoquinone monoketal chemistry. Experimental and density functional theory studies on orthoquinol acetate rearrangements. In Tetrahedron Letters (Vol. 40, Issue 4, p. 615-618). https://doi.org/10.1016/S0040-4039(98)02448-4
(). Synthetic uses of orthoquinone monoketals and their orthoquinol variants. A review. In Organic Preparations and Procedures International (Vol. 31, Issue 6, p. 617-680). https://doi.org/10.1080/00304949909355348
(). Novel preparation of orthoquinol acetates and their application in oxygen heterocyclization reactions. In Journal of Organic Chemistry (Vol. 63, Issue 25, p. 9597-9600). https://doi.org/10.1021/jo9817669
(). Lignin-ferulate cross-links in grasses. Part 4. Incorporation of 5-5-coupled dehydrodiferulate into synthetic lignin. In Journal of the Chemical Society Perkin Transactions 1 (Issue 16, p. 2351-2358). https://doi.org/10.1039/a701808h
(). Ellagitannin Chemistry. the First Synthesis of Dehydrohexahydroxydiphenoate Esters from Oxidative Coupling of Unetherified Methyl Gallate. In Journal of Organic Chemistry (Vol. 62, Issue 25, p. 8809-8813). https://doi.org/10.1021/jo971354k
(). p-Hydroxyphenyl, Guaiacyl, and Syringyl Lignins Have Similar Inhibitory Effects on Wall Degradability. In Journal of Agricultural and Food Chemistry (Vol. 45, Issue 7, p. 2530-2532). https://doi.org/10.1021/jf970029v
(). P-coumaroylated syringyl units in maize lignin: Implications for β- ether cleavage by thioacidolysis. In Phytochemistry (Vol. 43, Issue 6, p. 1189-1194). https://doi.org/10.1016/S0031-9422(96)00431-1
(). Galloyl-derived orthoquinones as reactive partners in nucleophilic additions and Diels-Alder dimerizations: A novel route to the dehydrodigalloyl linker unit of agrimoniin-type ellagitannins. In Journal of Organic Chemistry (Vol. 61, Issue 19, p. 6656-6665). https://doi.org/10.1021/jo961043u
(). Ellagitannin chemistry. In Chemical Reviews (Vol. 96, Issue 1, p. 475-503). https://doi.org/10.1021/cr940716a
(). Dehydrogenation polymer-cell wall complexes as a model for lignified grass walls. In Journal of Agricultural and Food Chemistry (Vol. 44, Issue 6, p. 1453-1459). https://doi.org/10.1021/jf9502717
(). Chemistry of Galloyl-Derived o-Quinones: Reactivity toward Nucleophiles. In Journal of Organic Chemistry (Vol. 60, Issue 16, p. 4982-4983). https://doi.org/10.1021/jo00121a012
(). Pathway of p-Coumaric Acid Incorporation into Maize Lignin As Revealed by NMR. In Journal of the American Chemical Society (Vol. 116, Issue 21, p. 9448-9456). https://doi.org/10.1021/ja00100a006
(). A biomimetic route to lignin model compounds via silver (I) oxide oxidation: 2. NMR characterization of non-cyclic benzyl aryl ether trimers and tetramers. In Holzforschung (Vol. 48, Issue 2, p. 124-132). https://doi.org/10.1515/hfsg.1994.48.2.124
(). Identification and synthesis of new ferulic acid dehydrodimers present in grass cell walls. In Journal of the Chemical Society Perkin Transactions 1 (Issue 23, p. 3485-3498). https://doi.org/10.1039/p19940003485
(). A Biomimetic Route to Lignin Model Compounds via Silver (I) Oxide Oxidation: 1. Synthesis of Dilignols and Non-Cyclic Benzyl Aryl Ethers. In Holzforschung (Vol. 48, Issue 1, p. 12-22). https://doi.org/10.1515/hfsg.1994.48.1.12
(). Synthesis of 4,8-bis(4-hydroxy-3-methoxyphenyl)-3,7-dioxabicyclo[3.3.0]octan-2-ones and determination of their relative configuration via long-range proton couplings. In Journal of the Chemical Society Perkin Transactions 1 (Issue 6, p. 653-659). https://doi.org/10.1039/P19930000653
(). Facile Large-Scale Synthesis of Coniferyl, Sinapyl, and p-Coumaryl Alcohol. In Journal of Agricultural and Food Chemistry (Vol. 40, Issue 7, p. 1108-1110). https://doi.org/10.1021/jf00019a003
(). Lignin-feruloyl ester cross-links in grasses. Part 1. Incorporation of feruloyl esters into coniferyl alcohol dehydrogenation polymers. In Journal of the Chemical Society Perkin Transactions 1 (Issue 21, p. 2961-2969). https://doi.org/10.1039/P19920002961