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Green Synthesis and Characterization of UV-Curable Multifunctional Rosin-Based Resins via Michael Addition Reaction.
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- Journal of Polymers & the Environment, 2024, v. 32, n. 9, p. 4567, doi. 10.1007/s10924-024-03253-1
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Preparation of a chiral hyperbranched polymer based on cinchona alkaloids and investigation of its catalytic activity in asymmetric reactions.
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- Turkish Journal of Chemistry, 2024, v. 48, n. 4, p. 512, doi. 10.55730/1300-0527.3677
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Methylthiouracil-modified Carbon Paste Electrode as a New Voltammetric Sensor Based on a 1,4-Michael Addition Reaction for Detection of Dopamine.
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- Electroanalysis, 2015, v. 27, n. 12, p. 2708, doi. 10.1002/elan.201500388
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1,4-Michael Addition - The Analytical Way for Quantitative Sensing of Neurotransmitter at Bare Gold Electrode in Physiological Solution in the Presence of Interfering Biogenic Compounds.
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- Electroanalysis, 2013, v. 25, n. 9, p. 2067, doi. 10.1002/elan.201300264
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Cupin Variants as a Macromolecular Ligand Library for Stereoselective Michael Addition of Nitroalkanes.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7791, doi. 10.1002/ange.202000129
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Diels–Alder Reactions During the Biosynthesis of Sorbicillinoids.
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- Angewandte Chemie, 2020, v. 132, n. 14, p. 5865, doi. 10.1002/ange.201915486
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Biomimetic Synthesis of Rhytidenone A and Mode of Action of Cytotoxic Rhytidenone F.
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- Angewandte Chemie, 2020, v. 132, n. 10, p. 4144, doi. 10.1002/ange.201914257
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Halide Anion Triggered Reactions of Michael Acceptors with Tropylium Ion.
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- Angewandte Chemie, 2020, v. 132, n. 4, p. 1471, doi. 10.1002/ange.201910578
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Metal‐Free Synthesis of Functional 1‐Substituted‐1,2,3‐Triazoles from Ethenesulfonyl Fluoride and Organic Azides.
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- Angewandte Chemie, 2020, v. 132, n. 3, p. 1197, doi. 10.1002/ange.201912728
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Synergic Interplay Between Halogen Bonding and Hydrogen Bonding in the Activation of a Neutral Substrate in a Nanoconfined Space.
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- Angewandte Chemie, 2020, v. 132, n. 2, p. 821, doi. 10.1002/ange.201909865
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A Genetically Encoded, Phage‐Displayed Cyclic‐Peptide Library.
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- Angewandte Chemie, 2019, v. 131, n. 44, p. 16051, doi. 10.1002/ange.201908713
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Total Synthesis of (−)‐Indoxamycins A and B.
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- Angewandte Chemie, 2019, v. 131, n. 20, p. 6731, doi. 10.1002/ange.201902043
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One‐Pot Catalytic Enantioselective Synthesis of 2‐Pyrazolines.
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- Angewandte Chemie, 2019, v. 131, n. 8, p. 2491, doi. 10.1002/ange.201811471
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Highly Reactive and Tracelessly Cleavable Cysteine‐Specific Modification of Proteins via 4‐Substituted Cyclopentenone.
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- Angewandte Chemie, 2018, v. 130, n. 36, p. 11772, doi. 10.1002/ange.201804801
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On‐Line Polyketide Cyclization into Diverse Medium‐Sized Lactones by a Specialized Ketosynthase Domain.
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- Angewandte Chemie, 2018, v. 130, n. 35, p. 11393, doi. 10.1002/ange.201804991
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Asymmetric Synthesis of Spirocyclic β‐Lactams through Copper‐Catalyzed Kinugasa/Michael Domino Reactions.
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- Angewandte Chemie, 2018, v. 130, n. 34, p. 11151, doi. 10.1002/ange.201806931
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Modular One‐Step Three‐Component Synthesis of Tetrahydroisoquinolines Using a Catellani Strategy.
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- Angewandte Chemie, 2018, v. 130, n. 34, p. 11146, doi. 10.1002/ange.201806780
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Heteroannulation of Arynes with α‐Amino Imides: Synthesis of 2,2‐Disubstituted Indolin‐3‐ones and Application to the Enantioselective Total Synthesis of (+)‐Hinckdentine A.
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- Angewandte Chemie, 2018, v. 130, n. 20, p. 5781, doi. 10.1002/ange.201800746
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2‐Hydroxybenzophenone as a Chemical Auxiliary for the Activation of Ketiminoesters for Highly Enantioselective Addition to Nitroalkenes under Bifunctional Catalysis.
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- Angewandte Chemie, 2018, v. 130, n. 19, p. 5448, doi. 10.1002/ange.201800435
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Stereodivergent Evolution of Artificial Enzymes for the Michael Reaction.
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- Angewandte Chemie, 2018, v. 130, n. 19, p. 5386, doi. 10.1002/ange.201712554
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Titelbild: Catalyst‐Enabled Site‐Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl Acceptors (Angew. Chem. 17/2018).
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- Angewandte Chemie, 2018, v. 130, n. 17, p. 4519, doi. 10.1002/ange.201802880
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Catalyst‐Enabled Site‐Divergent Stereoselective Michael Reactions: Overriding Intrinsic Reactivity of Enynyl Carbonyl Acceptors.
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- Angewandte Chemie, 2018, v. 130, n. 17, p. 4822, doi. 10.1002/ange.201800057
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Highly Enantioselective Tandem Michael Addition of Tryptamine‐Derived Oxindoles to Alkynones: Concise Synthesis of Strychnos Alkaloids.
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- Angewandte Chemie, 2018, v. 130, n. 14, p. 3868, doi. 10.1002/ange.201800567
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Kinetic Resolution of <italic>sec</italic>‐Thiols by Enantioselective Oxidation with Rationally Engineered 5‐(Hydroxymethyl)furfural Oxidase.
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- Angewandte Chemie, 2018, v. 130, n. 11, p. 2914, doi. 10.1002/ange.201713189
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Die katalytische, asymmetrische Mukaiyama‐Michael‐Reaktion von Silylketenacetalen mit α,β‐ungesättigten Methylestern.
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- Angewandte Chemie, 2018, v. 130, n. 9, p. 2489, doi. 10.1002/ange.201712088
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Total Synthesis of (+)‐Gracilamine Based on an Oxidative Phenolic Coupling Reaction and Determination of Its Absolute Configuration.
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- Angewandte Chemie, 2018, v. 130, n. 8, p. 2251, doi. 10.1002/ange.201708575
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Innenrücktitelbild: Direct Asymmetric Michael Reaction of α,β‐Unsaturated Aldehydes and Ketones Catalyzed by Two Secondary Amine Catalysts (Angew. Chem. 7/2018).
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- Angewandte Chemie, 2018, v. 130, n. 7, p. 2023, doi. 10.1002/ange.201800065
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Direct Asymmetric Michael Reaction of α,β‐Unsaturated Aldehydes and Ketones Catalyzed by Two Secondary Amine Catalysts.
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- Angewandte Chemie, 2018, v. 130, n. 7, p. 1976, doi. 10.1002/ange.201710085
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Total Syntheses of the Monoterpenoid Indole Alkaloids (±)-Alstoscholarisine B and C.
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- Angewandte Chemie, 2017, v. 129, n. 52, p. 16901, doi. 10.1002/ange.201710943
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One-Step Multigram-Scale Biomimetic Synthesis of Psiguadial B.
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- Angewandte Chemie, 2017, v. 129, n. 44, p. 13964, doi. 10.1002/ange.201708333
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Aryloxide-Facilitated Catalyst Turnover in Enantioselective α,β-Unsaturated Acyl Ammonium Catalysis.
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- Angewandte Chemie, 2017, v. 129, n. 40, p. 12450, doi. 10.1002/ange.201706402
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SuFEx-Based Polysulfonate Formation from Ethenesulfonyl Fluoride-Amine Adducts.
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- Angewandte Chemie, 2017, v. 129, n. 37, p. 11355, doi. 10.1002/ange.201701160
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Total Synthesis of Homodimericin A.
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- Angewandte Chemie, 2017, v. 129, n. 27, p. 8003, doi. 10.1002/ange.201702893
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N-Heterocyclic Carbene Catalyzed [4+2] Annulation of Enals via a Double Vinylogous Michael Addition: Asymmetric Synthesis of 3,5-Diaryl Cyclohexenones.
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- Angewandte Chemie, 2017, v. 129, n. 22, p. 6337, doi. 10.1002/ange.201702881
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Organocatalytic, Enantioselective Synthesis of Cyclohexadienone Containing Hindered Spirocyclic Ethers through an Oxidative Dearomatization/Oxa-Michael Addition Sequence.
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- Angewandte Chemie, 2016, v. 128, n. 48, p. 15339, doi. 10.1002/ange.201607039
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Enantio- and Diastereoselective Synthesis of exo-Peroxyacetals: An Organocatalyzed Peroxyhemiacetalization/oxa-Michael Addition Cascade.
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- Angewandte Chemie, 2016, v. 128, n. 27, p. 7854, doi. 10.1002/ange.201511165
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Development of a Divergent Synthetic Route to the Erythrina Alkaloids: Asymmetric Syntheses of 8-Oxo-erythrinine, Crystamidine, 8-Oxo-erythraline, and Erythraline.
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- Angewandte Chemie, 2016, v. 128, n. 24, p. 7029, doi. 10.1002/ange.201602650
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In Situ Observation of Thiol Michael Addition to a Reversible Covalent Drug in a Crystalline Sponge.
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- Angewandte Chemie, 2016, v. 128, n. 16, p. 5003, doi. 10.1002/ange.201509801
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Rapid Access to 2-Methylene Tetrahydrofurans and γ-Lactones: A Tandem Four-Step Process.
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- Angewandte Chemie, 2016, v. 128, n. 7, p. 2633, doi. 10.1002/ange.201511133
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Exocyclic Olefinic Maleimides: Synthesis and Application for Stable and Thiol-Selective Bioconjugation.
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- Angewandte Chemie, 2016, v. 128, n. 4, p. 1454, doi. 10.1002/ange.201508118
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Enantioselective Aza Michael-Type Addition to Alkenyl Benzimidazoles Catalyzed by a Chiral Phosphoric Acid.
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- Angewandte Chemie, 2016, v. 128, n. 3, p. 939, doi. 10.1002/ange.201508231
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Highly Enantioselective Aza-Michael Reaction between Alkyl Amines and β-Trifluoromethyl β-Aryl Nitroolefins.
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- Angewandte Chemie, 2015, v. 127, n. 51, p. 15634, doi. 10.1002/ange.201508371
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Asymmetric Dearomatization of β-Naphthols through a Bifunctional-Thiourea-Catalyzed Michael Reaction.
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- Angewandte Chemie, 2015, v. 127, n. 49, p. 15142, doi. 10.1002/ange.201507998
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Direct Catalytic Asymmetric Doubly Vinylogous Michael Addition of α,β-Unsaturated γ-Butyrolactams to Dienones.
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- Angewandte Chemie, 2015, v. 127, n. 35, p. 10387, doi. 10.1002/ange.201504276
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Selective Michael Reaction Controlled by Supersilyl Protecting Group.
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- Angewandte Chemie, 2015, v. 127, n. 30, p. 8821, doi. 10.1002/ange.201503574
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A Promiscuous De Novo Retro-Aldolase Catalyzes Asymmetric Michael Additions via Schiff Base Intermediates.
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- Angewandte Chemie, 2015, v. 127, n. 19, p. 5701, doi. 10.1002/anie.201500217
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A Metal-Ligand Cooperative Pathway for Intermolecular Oxa-Michael Additions to Unsaturated Nitriles.
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- Angewandte Chemie, 2015, v. 127, n. 14, p. 4310, doi. 10.1002/ange.201412110
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Asymmetric Dearomatization of Indoles through a Michael/Friedel-Crafts-Type Cascade To Construct Polycyclic Spiroindolines.
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- Angewandte Chemie, 2015, v. 127, n. 13, p. 4104, doi. 10.1002/ange.201410814
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Histidine-Containing Peptide Catalysts Developed by a Facile Library Screening Method.
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- Angewandte Chemie, 2015, v. 127, n. 6, p. 1842, doi. 10.1002/ange.201410268
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Hydrogen-Borrowing and Interrupted-Hydrogen-Borrowing Reactions of Ketones and Methanol Catalyzed by Iridium.
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- Angewandte Chemie, 2015, v. 127, n. 5, p. 1662, doi. 10.1002/ange.201410391
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