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ortho‐Quinols in (Bio)Synthesis of Natural Products.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 13, p. 1, doi. 10.1002/ejoc.202201224
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- Article
Novel 7-Chloro-(4-thioalkylquinoline) Derivatives: Synthesis and Antiproliferative Activity through Inducing Apoptosis and DNA/RNA Damage.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 10, p. 1234, doi. 10.3390/ph15101234
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- Article
Preparation of a ε-caprolactonic diterpenoid derivate by unexpected oxidative cleavage/lactonization of 2-oxoaustroeupatol.
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- Natural Products & Bioprospecting, 2022, v. 12, n. 1, p. 1, doi. 10.1007/s13659-022-00343-2
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- Article
Bispericyclic Diels–Alder Dimerization of ortho‐Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6‐Step Synthesis of (+)‐Maytenone.
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- Angewandte Chemie, 2021, v. 133, n. 27, p. 15094, doi. 10.1002/ange.202103410
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Innenrücktitelbild: Bispericyclic Diels–Alder Dimerization of ortho‐Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6‐Step Synthesis of (+)‐Maytenone (Angew. Chem. 27/2021).
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- Angewandte Chemie, 2021, v. 133, n. 27, p. 15239, doi. 10.1002/ange.202106111
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- Article
Bispericyclic Diels–Alder Dimerization of ortho‐Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6‐Step Synthesis of (+)‐Maytenone.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 27, p. 14967, doi. 10.1002/anie.202103410
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- Article
Inside Back Cover: Bispericyclic Diels–Alder Dimerization of ortho‐Quinols in Natural Product (Bio)Synthesis: Bioinspired Chemical 6‐Step Synthesis of (+)‐Maytenone (Angew. Chem. Int. Ed. 27/2021).
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- Angewandte Chemie International Edition, 2021, v. 60, n. 27, p. 15111, doi. 10.1002/anie.202106111
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- Article
Real‐Time Analysis of Polyphenol–Protein Interactions by Surface Plasmon Resonance Using Surface‐Bound Polyphenols.
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- Chemistry - A European Journal, 2021, v. 27, n. 17, p. 5498, doi. 10.1002/chem.202005187
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- Article
Synthesis and leishmanicidal evaluation of sulfanyl‐ and sulfonyl‐tethered functionalized benzoate derivatives featuring a nitroimidazole moiety.
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- Archiv der Pharmazie, 2020, v. 353, n. 5, p. 1, doi. 10.1002/ardp.202000002
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- Article
Innentitelbild: Blue LED Irradiation of Iodonium Ylides Gives Diradical Intermediates for Efficient Metal‐free Cyclopropanation with Alkenes (Angew. Chem. 47/2019).
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- Angewandte Chemie, 2019, v. 131, n. 47, p. 16854, doi. 10.1002/ange.201912827
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- Article
Blue LED Irradiation of Iodonium Ylides Gives Diradical Intermediates for Efficient Metal‐free Cyclopropanation with Alkenes.
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- Angewandte Chemie, 2019, v. 131, n. 47, p. 17115, doi. 10.1002/ange.201908994
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- Article
Inside Cover: Blue LED Irradiation of Iodonium Ylides Gives Diradical Intermediates for Efficient Metal‐free Cyclopropanation with Alkenes (Angew. Chem. Int. Ed. 47/2019).
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- Angewandte Chemie International Edition, 2019, v. 58, n. 47, p. 16700, doi. 10.1002/anie.201912827
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- Article
Blue LED Irradiation of Iodonium Ylides Gives Diradical Intermediates for Efficient Metal‐free Cyclopropanation with Alkenes.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 47, p. 16959, doi. 10.1002/anie.201908994
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- Article
Bio‐inspired Total Synthesis of Twelve Securinega Alkaloids: Structural Reassignments of (+)‐Virosine B and (−)‐Episecurinol A.
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- Chemistry - A European Journal, 2019, v. 25, n. 49, p. 11574, doi. 10.1002/chem.201903122
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- Article
Synthesis of [7]Helicene Enantiomers and Exploratory Study of Their Conversion into Helically Chiral Iodoarenes and Iodanes.
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- Chemistry - A European Journal, 2019, v. 25, n. 11, p. 2852, doi. 10.1002/chem.201805761
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- Article
Bioinspired Total Synthesis of (−)-Vescalin: A Nonahydroxytriphenoylated C-Glucosidic Ellagitannin.
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- Angewandte Chemie, 2017, v. 129, n. 44, p. 14021, doi. 10.1002/ange.201707613
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- Article
Bioinspired Total Synthesis of (−)-Vescalin: A Nonahydroxytriphenoylated C-Glucosidic Ellagitannin.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 44, p. 13833, doi. 10.1002/anie.201707613
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- Article
Asymmetric Alkynylation of β-Ketoesters and Naphthols Promoted by New Chiral Biphenylic Iodanes.
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- Chemistry - A European Journal, 2017, v. 23, n. 54, p. 13309, doi. 10.1002/chem.201703238
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- Article
Gallotannins and Tannic Acid: First Chemical Syntheses and In Vitro Inhibitory Activity on Alzheimer's Amyloid b-Peptide Aggregation.
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- Angewandte Chemie, 2015, v. 127, n. 28, p. 8335, doi. 10.1002/ange.201411606
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Gallotannins and Tannic Acid: First Chemical Syntheses and In Vitro Inhibitory Activity on AlzheimerÏs Amyloid b-Peptide Aggregation.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 28, p. 8217, doi. 10.1002/anie.201411606
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Asymmetric Hydroxylative Phenol Dearomatization Promoted by Chiral Binaphthylic and Biphenylic Iodanes.
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- Angewandte Chemie, 2014, v. 126, n. 37, p. 10018, doi. 10.1002/ange.201403571
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Asymmetric Hydroxylative Phenol Dearomatization Promoted by Chiral Binaphthylic and Biphenylic Iodanes.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 37, p. 9860, doi. 10.1002/anie.201403571
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- Article
Protecting-Group-Free Solid-Phase Anchoring of Polyphenolic C-Glucosidic Ellagitannins and Synthesis of 1-Alkylamino-Vescalagin Derivatives (Eur. J. Org. Chem. 23/2014).
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 23, p. n/a, doi. 10.1002/ejoc.201490063
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- Article
Protecting-Group-Free Solid-Phase Anchoring of Polyphenolic C-Glucosidic Ellagitannins and Synthesis of 1-Alkylamino-Vescalagin Derivatives.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 23, p. 4963, doi. 10.1002/ejoc.201402444
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- Article
Remarkable Biomimetic Chemoselective Aerobic Oxidation of Flavano-Ellagitannins Found in Oak-Aged Wine.
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- Angewandte Chemie, 2013, v. 125, n. 44, p. 11744, doi. 10.1002/ange.201305839
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- Article
Remarkable Biomimetic Chemoselective Aerobic Oxidation of Flavano-Ellagitannins Found in Oak-Aged Wine.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 44, p. 11530, doi. 10.1002/anie.201305839
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- Article
Synthetic Studies toward C-Glucosidic Ellagitannins: A Biomimetic Total Synthesis of 5- O-Desgalloylepipunicacortein A.
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- Chemistry - A European Journal, 2012, v. 18, n. 29, p. 9063, doi. 10.1002/chem.201200517
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- Article
Resveratrol: Die Geschichte geht weiter.
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- Angewandte Chemie, 2012, v. 124, n. 28, p. 6930, doi. 10.1002/ange.201203059
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Resveratrol Still Has Something To Say about Aging!
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- Angewandte Chemie International Edition, 2012, v. 51, n. 28, p. 6824, doi. 10.1002/anie.201203059
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New Triterpenoid and Ergostane Glycosides from the Leaves of Hydrocotyle umbellata L.
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- Helvetica Chimica Acta, 2011, v. 94, n. 10, p. 1850, doi. 10.1002/hlca.201100109
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Pflanzliche Polyphenole: chemische Eigenschaften, biologische Aktivität und Synthese.
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- Angewandte Chemie, 2011, v. 123, n. 3, p. 610, doi. 10.1002/ange.201000044
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Plant Polyphenols: Chemical Properties, Biological Activities, and Synthesis.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 3, p. 586, doi. 10.1002/anie.201000044
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- Article
Highly Diastereoselective Synthesis of Orthoquinone Monoketals through λ<sup>3</sup>-Iodane-Mediated Oxidative Dearomatization of Phenols.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 19, p. 3552, doi. 10.1002/anie.200705816
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A Convenient Synthesis of the Echinacea-Derived Immunostimulator and HIV-1 Integrase Inhibitor (−)-(2 R,3 R)-Chicoric Acid.
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- Helvetica Chimica Acta, 2002, v. 85, n. 8, p. 2328, doi. 10.1002/1522-2675(200208)85:8<2328::AID-HLCA2328>3.0.CO;2-X
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- Article