Works matching DE "BAYLIS-Hillman reaction"
Results: 172
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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- Article
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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- Article
Azo dye-based colorimetric chemodosimeter for cyanide in aqueous solution.
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- Supramolecular Chemistry, 2013, v. 25, n. 1, p. 24, doi. 10.1080/10610278.2012.712121
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- Article
Synthesis and Anticholinesterase Activity of 3-{[4-Methyl-3-(4-methylpiperazin-1-yl)]pent-1-en-1-yl}-4H-chromen-4-ones.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 12, p. 2471, doi. 10.1134/S1070363219120235
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- Article
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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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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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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Enantioselective Allylic Amination of Morita-Baylis-Hillman Acetates Catalyzed by Chiral Thiourea-Phosphine.
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- Chinese Journal of Chemistry, 2015, v. 33, n. 12, p. 1333, doi. 10.1002/cjoc.201500697
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Enatioselective Chalcogeno-Baylis-Hillman Reaction of Arylaldehydes with MVK and Acrylates Catalyzed by Chiral Thiepin-TiCl<sub>4</sub> Complex.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 4, p. 365, doi. 10.1002/cjoc.201400077
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- Article
Phosphine-Catalyzed Enantioselective γ-Addition of 3-Substituted Oxindoles to 2,3-Butadienoates and 2-Butynoates: Use of Prochiral Nucleophiles.
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- Angewandte Chemie, 2014, v. 126, n. 11, p. 3008, doi. 10.1002/ange.201307757
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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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Transformations of Modified Morita‐Baylis‐Hillman Adducts from Isatins Catalyzed by Lewis Bases.
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- Chemical Record, 2020, v. 20, n. 6, p. 541, doi. 10.1002/tcr.201900058
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Mass Spectrometric Back Reaction Screening of Quasi-Enantiomeric Products as a Mechanistic Tool.
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- Chemical Record, 2016, v. 16, n. 6, p. 2534, doi. 10.1002/tcr.201600072
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Synthesis and Characterization with Computational Studies of Metal Complexes of Methyl 2-((4-cyanophenyl)(hydroxy) methyl)acrylate: A New Biologically Active Multi-Functional Adduct.
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- Separations (2297-8739), 2022, v. 9, n. 10, p. N.PAG, doi. 10.3390/separations9100306
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Photophysical and In Vitro-In Silico Studies on Newly Synthesized Ethyl 3-((3-Methyl-1-phenyl-1H-pyrazol-5-yl)oxy)-2-methyleneheptanoate.
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- Russian Journal of Organic Chemistry, 2024, v. 60, n. 7, p. 1176, doi. 10.1134/S1070428024070066
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Synthesis and Transformations of the Adduct of 1-Phenyltricyclo[4.1.0.02,7]heptane with 2-Bromoethanesulfonyl Bromide.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 5, p. 746, doi. 10.1134/S1070428020050048
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- Article
Imidazolyl Alanes – Synthesis, Structures, and Reactivity Studies.
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- European Journal of Inorganic Chemistry, 2020, v. 2020, n. 19, p. 1906, doi. 10.1002/ejic.202000174
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Synthesis of a T‐Shaped Cobalt(I) Complex and Its Dinitrogen Adduct.
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- European Journal of Inorganic Chemistry, 2020, v. 2020, n. 15/16, p. 1465, doi. 10.1002/ejic.201901129
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Taming Copper(I) Cyanate and Selenocyanate with N‐Heterocyclic Carbenes.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 31, p. 3581, doi. 10.1002/ejic.201900515
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Phosphinic Dehydrodipeptides: Diversification of the P1′ Residue with the Morita–Baylis–Hillman Acetates and Inhibition of Alanyl Aminopeptidases.
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- International Journal of Peptide Research & Therapeutics, 2020, v. 26, n. 4, p. 2109, doi. 10.1007/s10989-019-10004-7
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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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Tertiary Amine-Catalyzed Difluoromethylthiolation of Morita-Baylis-Hillman Carbonates of Isatins with Zard's Trifluoromethylthiolation Reagent.
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- Advanced Synthesis & Catalysis, 2017, v. 359, n. 1, p. 49, doi. 10.1002/adsc.201600954
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Chemoselectivity Improvement via Partial Shielding of an Imidazole Active Site in Branched/Dendritic Homogeneous Catalysts of the Baylis-Hillman Reaction.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 22, p. 3541, doi. 10.1002/adsc.201600421
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Chiral Phosphine-Catalyzed Enantioselective [3+2] Annulation of Morita-Baylis-Hillman Carbonates with Cyclic 1-Azadienes: Synthesis of Functionalized Cyclopentenes.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 22, p. 3517, doi. 10.1002/adsc.201600607
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Asymmetric Construction of Highly Functionalized Spirobarbiturate-Cyclopentenes through Chiral Phosphine-Catalyzed [3+2] Annulation of Morita-Baylis-Hillman Carbonates with Barbiturate-Derived Alkenes.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 18, p. 2867, doi. 10.1002/adsc.201600450
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Rhodium-Catalyzed [2+2+2] Cycloadditions of Diynes with Morita-Baylis-Hillman Adducts: A Stereoselective Entry to Densely Functionalized Cyclohexadiene Scaffolds.
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- 2016
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- Other
Organocatalytic Enantioselective Reaction of Cyclopent-2-enone-Derived Morita-Baylis-Hillman Alcohols with 4-Hydroxycoumarins.
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- 2016
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- Other
Tunable Bifunctional Phosphine-Squaramide Promoted Morita-Baylis-Hillman Reaction of N-Alkyl Isatins with Acrylates.
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- 2015
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- Other
Asymmetric N-Allylic Alkylation of Hydrazones with Morita-Baylis-Hillman Carbonates.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 2/3, p. 384, doi. 10.1002/adsc.201400790
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An Expeditious and Metal-Free Synthetic Route towards Quinolones, Naphthyridones and Benzonaphthyridones.
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- Advanced Synthesis & Catalysis, 2014, v. 356, n. 17, p. 3600, doi. 10.1002/adsc.201300891
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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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- Article
A Note on Morita Equivalence Preserving Functor from the Category of Semigroups to the Category of Semirings.
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- Southeast Asian Bulletin of Mathematics, 2019, v. 43, n. 2, p. 297
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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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Enantioselective Aza-Morita-Baylis-Hillman Reaction with Ketimines and Acrolein Catalyzed by Organic Assemblies.
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- Chemistry - A European Journal, 2013, v. 19, n. 29, p. 9447, doi. 10.1002/chem.201301558
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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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Fast, microwave-promoted one-pot synthesis of bicyclic pyrimidones from Baylis-Hillman adducts.
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- Journal of Chemical Research, 2015, v. 39, n. 2, p. 63, doi. 10.3184/174751915X14199645231447
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Efficient synthesis of pyrazole fused [6-7-5] tricyclic frameworks via intramolecular Friedel-Crafts reaction of Morita-Baylis-Hillman adducts.
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- Journal of Chemical Research, 2014, v. 38, n. 2, p. 85, doi. 10.3184/174751914X13891972597451
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Morita Baylis Hillman Adduct Serves as Ligand in the Synthesis of Transition Metal Complexes Exhibiting Antibacterial Activity.
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- Pharmaceutical Chemistry Journal, 2022, v. 56, n. 7, p. 906, doi. 10.1007/s11094-022-02725-9
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Enantioselective Morita-Baylis-Hillman Reaction of Acrylates with Nitrobenzaldehydes Promoted by the Bifunctional Ferrocene-Based Phosphinothiourea Organocatalysts.
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- Catalysis Letters, 2016, v. 146, n. 8, p. 1429, doi. 10.1007/s10562-016-1759-9
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Promiscuous Lipase-Catalyzed C-C Bond Formation Reactions Between 4 Nitrobenzaldehyde and 2-Cyclohexen-1-one in Biphasic Medium: Aldol and Morita-Baylis-Hillman Adduct Formations.
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- Catalysis Letters, 2015, v. 145, n. 2, p. 527, doi. 10.1007/s10562-014-1429-8
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- Article
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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- Article
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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Baylis-Hillman Reaction: In Situ Generated Isoquinolinium Species as Excellent Electrophiles for Coupling with Alkyl Acrylates and Acrylonitrile.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 34, p. 5135, doi. 10.1002/ejoc.201700743
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- Article
Synthesis of Angularly Fused Pyrrolo[3,2- c]quinoline Lactones and 4-Carboxy-3-vinyl-1,2-dihydroquinolin-2-ones from Morita-Baylis-Hillman Adducts with Labile Acrylate Esters as Michael Acceptors by [3+2] Cycloaddition and Hoffmann-Type Elimination.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 26, p. 3774, doi. 10.1002/ejoc.201700449
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- Article