Works matching DE "BAYLIS-Hillman reaction"
Results: 171
A Vicinal Diol Approach for the Total Synthesis of Molestin E, ent‐Sinulacembranolide A and ent‐Sinumaximol A.
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- Chemistry - A European Journal, 2022, v. 28, n. 63, p. 1, doi. 10.1002/chem.202202464
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Post‐Synthetic Modification of a Porous Hydrocarbon Cage to Give a Discrete Co<sub>24</sub> Organometallic Complex**.
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- Chemistry - A European Journal, 2022, v. 28, n. 51, p. 1, doi. 10.1002/chem.202200958
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Toward De Novo Catalyst Discovery: Fast Identification of New Catalyst Candidates for Alcohol‐Mediated Morita–Baylis–Hillman Reactions**.
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- Angewandte Chemie, 2023, v. 135, n. 49, p. 1, doi. 10.1002/ange.202310580
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Computational Evolution Of New Catalysts For The Morita–Baylis–Hillman Reaction**.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202218565
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Morita–Baylis–Hillman‐Type [3,3]‐Rearrangement: Switching from Z‐ to E‐Selective α‐Arylation by New Rearrangement Partners.
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- Angewandte Chemie, 2021, v. 133, n. 20, p. 11515, doi. 10.1002/ange.202100497
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Z‐Selective α‐Arylation of α,β‐Unsaturated Nitriles via [3,3]‐Sigmatropic Rearrangement.
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- Angewandte Chemie, 2021, v. 133, n. 5, p. 2369, doi. 10.1002/ange.202010740
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Concise Synthesis of (+)‐[<sup>13</sup>C<sub>4</sub>]‐Anatoxin‐a by Dynamic Kinetic Resolution of a Cyclic Iminium Ion.
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- Angewandte Chemie, 2020, v. 132, n. 28, p. 11460, doi. 10.1002/ange.202004464
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Pseudo‐Stereodivergent Synthesis of Enantioenriched Tetrasubstituted Alkenes by Cascade 1,3‐Oxo‐Allylation/Cope Rearrangement.
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- Angewandte Chemie, 2020, v. 132, n. 18, p. 7149, doi. 10.1002/ange.202000044
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Cooperative Tertiary Amine/Chiral Iridium Complex Catalyzed Asymmetric [4+3] and [3+3] Annulation Reactions.
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- Angewandte Chemie, 2019, v. 131, n. 42, p. 15163, doi. 10.1002/ange.201907797
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Auto‐Tandem Cooperative Catalysis Using Phosphine/Palladium: Reaction of Morita–Baylis–Hillman Carbonates and Allylic Alcohols.
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- Angewandte Chemie, 2019, v. 131, n. 12, p. 4076, doi. 10.1002/ange.201814403
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Brucine Diol-Catalyzed Enantioselective Morita-Baylis-Hillman Reaction in the Presence of Brucine N-Oxide.
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- Catalysts (2073-4344), 2021, v. 11, n. 2, p. 237, doi. 10.3390/catal11020237
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Metal-Free Organocatalysis.
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- Catalysts (2073-4344), 2018, v. 8, n. 5, p. 195, doi. 10.3390/catal8050195
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Regioselective addition-elimination of Morita-Baylis-Hillman adducts with 2-naphthol or phenol catalyzed by functionalized ionic liquids: a direct strategy to construct functional alkenes.
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- Canadian Journal of Chemistry, 2016, v. 94, n. 3, p. 211, doi. 10.1139/cjc-2015-0358
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Solvent issues in the Baylis-Hillman reaction of 5-hydroxymethyl furfural (HMF) and 5-glucosyloxymethyl furfural (GMF). Towards no-solvent conditions.
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- Pure & Applied Chemistry, 2019, v. 91, n. 7, p. 1149, doi. 10.1515/pac-2019-0215
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Designed model for the Morita-Baylis-Hillman reaction mechanism in the presence of CaO and CaO modified with ionic liquid as a solid base catalyst: a DFT and MP2 investigation.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2018, v. 137, n. 9, p. 1, doi. 10.1007/s00214-018-2306-0
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SYNTHESIS OF 2-AMINO-3-PHENYLPROPAN-1-OL COMPOUNDS FROM BAYLIS-HILLMAN DERIVATIVES, CARBON NANOTUBE, KINETIC, LIFETIME AND BIOLOGICAL STUDIES.
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- Rasayan Journal of Chemistry, 2018, v. 11, n. 1, p. 175, doi. 10.7324/RJC.2018.1111864
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Synthesis and Evaluation of Baylis-Hillman Reaction Derived Imidazole and Triazole Cinnamates as Antifungal Agents.
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- International Journal of Medicinal Chemistry, 2018, p. 1, doi. 10.1155/2018/5758076
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Stereospecific Assembly of Trisubstituted Alkenes via Photoinduced Nitrogen‐Centered Radical‐Triggered C—C Bond Cleavage/Functionalization of Oxime Esters.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 12, p. 1399, doi. 10.1002/cjoc.202300774
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Inside Cover Picture.
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- Chinese Journal of Chemistry, 2022, v. 40, n. 10, p. 1122, doi. 10.1002/cjoc.202290102
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Solvent‐Regulated Diastereodivergent [3 + 2] Annulations of CF<sub>3</sub>‐Containing Morita−Baylis−Hillman Carbonates with Cyclic Sulfonimines.
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- Chinese Journal of Chemistry, 2022, v. 40, n. 10, p. 1185, doi. 10.1002/cjoc.202200003
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A Preliminary Comparative Study of the Baylis–Hillman Reaction in Ionic Liquid Solution and Gelled Ionic Liquid.
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- Macromolecular Symposia, 2019, v. 385, n. 1, p. N.PAG, doi. 10.1002/masy.201800193
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Recent Advances in the Reaction of MBH Carbonates: Scope and Mechanism.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 10, p. 1, doi. 10.1002/ajoc.202400237
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Zinc‐Mediated Diastereoselective Annulation of Cyclopropanols with Alkylidenemalononitriles via Enolized Homoenolate.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 5, p. 1, doi. 10.1002/ajoc.202300114
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Synthesis of Acrylonitrile Derivatives via Visible Light‐induced Coupling Reaction of Morita‐Baylis‐Hillman Adducts with Tertiary Amines and α‐Trimethylsilyl Amines.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 2, p. 1, doi. 10.1002/ajoc.202100747
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Visible Light‐Triggered β‐Allylation of Indoles Using Baylis‐Hillman Bromides.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 8, p. 1213, doi. 10.1002/ajoc.202000268
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Phosphine‐Catalyzed Enantioselective [1+4] Annulation of Morita‐Baylis‐Hillman Carbonates with α,β‐Unsaturated Imines.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 2, p. 242, doi. 10.1002/ajoc.201800719
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Lewis‐Base‐Catalyzed Domino Reaction of Morita–Baylis–Hillman Carbonates of Isatins with Enolizable Cyclic Carbonyl Compounds: Stereoselective Access to Spirooxindole‐Pyrans.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 8, p. 1595, doi. 10.1002/ajoc.201800240
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Highly Efficient Asymmetric Morita–Baylis–Hillman Reaction Promoted by Chiral Aziridine-Phosphines.
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- Catalysts (2073-4344), 2022, v. 12, n. 4, p. 394, doi. 10.3390/catal12040394
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Kinetic Resolution in Transannular Morita-Baylis-Hillman Reaction: An Approximation to the Synthesis of Sesquiterpenes from Guaiane Family.
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- Catalysts (2073-4344), 2022, v. 12, n. 1, p. 67, doi. 10.3390/catal12010067
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Molecular Iodine: Efficient Catalyst for the Synthesis of Baylis- Hillman Adducts.
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- Orbital: The Electronic Journal of Chemistry, 2014, v. 6, n. 2, p. 44
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Open samarocene and ytterbocenes and their adducts with N-heterocyclic carbene (NHC) and imidazolin-2-thiones<sup>†</sup>.
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- Australian Journal of Chemistry, 2022, v. 75, n. 8/9, p. 636, doi. 10.1071/CH21326
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Ionic Thiourea Organocatalysis of the Morita-Baylis-Hillman Reaction.
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- Australian Journal of Chemistry, 2016, v. 69, n. 7, p. 759, doi. 10.1071/CH15596
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Convenient Synthesis of Dihydrobenzofuran‐Fused Spirocyclopentane‐1,2‐Diindolinone Scaffolds.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 45, p. 1, doi. 10.1002/ejoc.202400777
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Utilizing Baylis–Hillman Adducts Followed by Michael Addition/Elimination Reaction for the Synthesis of Unusual Conformationally Stable Molecules Governed by Aromatic Interactions.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 48, p. 1, doi. 10.1002/ejoc.202301109
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Chiral thiourea derivatives as organocatalyts in the enantioselective Morita-Baylis-Hillman reactions.
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- ARKIVOC: Online Journal of Organic Chemistry, 2020, v. 2020, p. 21, doi. 10.24820/ark.5550190.p011.072
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P-C bond formation in reactions of Morita-Baylis-Hillman adducts with phosphorus nucleophiles.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 324, doi. 10.3998/ark.5550190.p009.787
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Synthesis, lipase catalyzed kinetic resolution, and determination of the absolute configuration of enantiomers of the Morita-Baylis-Hillman adduct 3- hydroxy-2-methylenebutanenitrile.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 313, doi. 10.3998/ark.5550190.p009.749
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Intramolecular Baylis-Hillman reaction: synthesis of heterocyclic molecules.
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- ARKIVOC: Online Journal of Organic Chemistry, 2016, p. 172, doi. 10.3998/ark.5550190.p009.322
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(S)-Garner aldehyde derived Baylis-Hillman adduct: a substrate for the synthesis of a lactone ceramide analogue via a sequential Heck reaction.
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 148
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Elucidation of the Complex Baylis-Hillman Reaction of 3-Methoxy-2-nitrobenzaldehyde with Methyl Vinyl Ketone.
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- South African Journal of Chemistry, 2011, v. 64, p. 144
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Towards a converged strategy for including microsolvation in reaction mechanism calculations.
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- Journal of Computer-Aided Molecular Design, 2021, v. 35, n. 4, p. 473, doi. 10.1007/s10822-020-00366-2
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Synthesis of chitosan- graft-poly[2-cyano-1-(pyridin-3-yl)allyl acrylate] copolymer from a novel monomer, prepared using a Morita-Baylis-Hillman reaction, and characterization of its antimicrobial activity.
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- Polymer International, 2014, v. 63, n. 12, p. 2042, doi. 10.1002/pi.4760
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Crystallization of Complexes of Nitrilotriacetic Acid with Organic Amines. Molecular Structure of Hexamethylene-1,6-Diammonium Nitrilotriacetate.
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- Crystallography Reports, 2022, v. 67, n. 2, p. 178, doi. 10.1134/S1063774522020158
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Morita-Baylis-Hillman Adducts Display Anti-Inflammatory Effects by Modulating Inflammatory Mediator Expression in RAW264.7 Cells.
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- Mediators of Inflammation, 2017, p. 1, doi. 10.1155/2017/6898505
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A Short Multistep Flow Synthesis of a Potential Spirocyclic Fragrance Component.
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- Chemical Engineering & Technology, 2015, v. 38, n. 10, p. 1713, doi. 10.1002/ceat.201500255
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The synthesis of a copper metal‐organic framework Cu<sub>3</sub>TDPAT and its application in a Morita‐Baylis‐Hillman (MBH) reaction.
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- Applied Organometallic Chemistry, 2022, v. 36, n. 3, p. 1, doi. 10.1002/aoc.6566
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Organocatalytic (1+4)‐Annulations of MBH Adducts with Electron‐Deficient Systems.
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- Chemical Record, 2023, v. 23, n. 11, p. 1, doi. 10.1002/tcr.202300152
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Environmentally Compatible Access to α‐Trifluoromethylseleno‐Enones.
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- Helvetica Chimica Acta, 2020, v. 103, n. 11, p. 1, doi. 10.1002/hlca.202000185
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Stereoselective Synthesis of ( Z)- and ( E)-Allyl Aryl Sulfides and Selenides from Baylis Hillman Acetates under Neutral Conditions Using β-Cyclodextrin in Water.
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- Helvetica Chimica Acta, 2013, v. 96, n. 12, p. 2276, doi. 10.1002/hlca.201300067
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Catalyst-free synthesis of 3-alkenyloxindoles from isatin-derived Morita-Baylis-Hillman carbonates.
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- Journal of Chemical Research, 2017, v. 41, n. 3, p. 160, doi. 10.3184/174751917X14878812592652
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