Works matching DE "ALLYLIC alkylation"
Results: 268
Rh(I)/Sulfoxide‐Imine‐Olefin Complex Catalyzed Enantioselective Allylic Alkylation of 2‐Fluoromalonate: Synthesis of Chiral α‐Fluorolactone Bearing Vicinal Stereogenic Centers.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402875
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- Article
Cobalt‐Catalyzed Allylic Alkylation at sp<sup>3</sup>‐Carbon Centers.
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- Chemistry - A European Journal, 2024, v. 30, n. 47, p. 1, doi. 10.1002/chem.202401707
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- Article
Cover Feature: Asymmetric Synthesis of Quaternary α‐Aryl Stereocentres in Benzofuran‐3(2H)‐Ones Using Decarboxylative Asymmetric Allylic Alkylation (Chem. Eur. J. 46/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 46, p. 1, doi. 10.1002/chem.202484602
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- Article
Asymmetric Synthesis of Quaternary α‐Aryl Stereocentres in Benzofuran‐3(2H)‐Ones Using Decarboxylative Asymmetric Allylic Alkylation.
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- Chemistry - A European Journal, 2024, v. 30, n. 46, p. 1, doi. 10.1002/chem.202401738
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- Article
Enantioselective Synthesis of α‐Quaternary Isochromanes by Oxidative Aminocatalysis and Gold Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 38, p. 1, doi. 10.1002/chem.202401354
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- Article
A Pd‐Catalyzed Annulation Strategy to Linearly Fused Functionalized N‐Heterocycles.
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- Chemistry - A European Journal, 2024, v. 30, n. 21, p. 1, doi. 10.1002/chem.202400116
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- Article
Aerobic Asymmetric Allylic C−H Alkylation by Synergistic Chiral Primary Amine‐Palladium‐Hydroquinone Catalysis.
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- Chemistry - A European Journal, 2024, v. 30, n. 16, p. 1, doi. 10.1002/chem.202304316
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- Article
Combining Enantioselective Rh‐Catalyzed Conjugate Addition and Ir‐Catalyzed Allylic Alkylation in Stereodivergent, Multicomponent Coupling Reactions to Form Three Stereocenters.
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202300727
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- Article
Efficient Synthesis of Diaryl Quaternary Centers by Rh(II)/Xantphos Catalyzed Relay C−H Functionalization and Allylic Alkylation.
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- Chemistry - A European Journal, 2023, v. 29, n. 3, p. 1, doi. 10.1002/chem.202202820
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- Article
Influence of Achiral Phosphine Ligands on a Synergistic Organo‐ and Palladium‐Catalyzed Asymmetric Allylic Alkylation.
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- Chemistry - A European Journal, 2022, v. 28, n. 71, p. 1, doi. 10.1002/chem.202202951
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- Article
Reagent optimization for allylic oxidation of 3- O-acetyl-β-boswellic acid into 3- O-acetyl-11-oxo-β-boswellic acid.
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- Chemistry of Natural Compounds, 2013, v. 48, n. 6, p. 1008, doi. 10.1007/s10600-013-0451-1
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- Article
Origins of Enhanced Enantioselectivity in the Pd-Catalyzed Decarboxylative Allylic Alkylation of N -Benzoyl Lactams †.
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- Catalysts (2073-4344), 2023, v. 13, n. 9, p. 1258, doi. 10.3390/catal13091258
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- Article
Synthesis, Characterization, Solution Behavior and Theoretical Studies of Pd(II) Allyl Complexes with 2-Phenyl-3H-indoles as Ligands.
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- Catalysts (2073-4344), 2019, v. 9, n. 10, p. 811, doi. 10.3390/catal9100811
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- Article
Copper(I)-catalyzed asymmetric alkylation of α-imino-esters.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37967-y
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Palladium-Catalyzed Allylic Alkylation of Simple Ketones with Allylic Alcohols and Its Mechanistic Study.
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- Angewandte Chemie, 2014, v. 126, n. 26, p. 6894, doi. 10.1002/ange.201403410
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- Article
Dual Platinum and Pyrrolidine Catalysis in the Direct Alkylation of Allylic Alcohols: Selective Synthesis of Monoallylation Products.
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- Angewandte Chemie, 2014, v. 126, n. 17, p. 4466, doi. 10.1002/ange.201311200
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- Article
Allylic Functionalization of Unactivated Olefins with Grignard Reagents.
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- Angewandte Chemie, 2014, v. 126, n. 6, p. 1690, doi. 10.1002/ange.201309134
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- Article
Copper-Free Asymmetric Allylic Alkylation of Trisubstituted Cyclic Allyl Bromides Using Grignard Reagents.
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- Angewandte Chemie, 2013, v. 125, n. 51, p. 13887, doi. 10.1002/ange.201307591
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- Article
Palladium-Catalyzed Asymmetric Construction of Vicinal All-Carbon Quaternary Stereocenters and its Application to the Synthesis of Cyclotryptamine Alkaloids.
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- Angewandte Chemie, 2013, v. 125, n. 35, p. 9346, doi. 10.1002/ange.201302805
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- Article
Total Synthesis of (−)-Melotenine A.
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- Angewandte Chemie, 2013, v. 125, n. 32, p. 8467, doi. 10.1002/ange.201302517
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- Article
Enantioselective Construction of α-Quaternary Cyclobutanones by Catalytic Asymmetric Allylic Alkylation.
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- Angewandte Chemie, 2013, v. 125, n. 26, p. 6850, doi. 10.1002/ange.201301815
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- Article
Construction of Enantiomerically Enriched Diazo Compounds Using Diazo Esters as Nucleophiles: Chiral Lewis Base Catalysis.
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- Angewandte Chemie, 2013, v. 125, n. 24, p. 6408, doi. 10.1002/ange.201301509
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- Article
Control of Selectivity in Palladium-Catalyzed Oxidative Carbocyclization/Borylation of Allenynes.
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- Angewandte Chemie, 2013, v. 125, n. 24, p. 6403, doi. 10.1002/ange.201301167
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- Article
Stereoselective Synthesis of Glycosides via Tsuji–Trost Type Glycosylation Using 3,4‐Carbonate Galactals.
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- Chemical Record, 2024, v. 24, n. 9, p. 1, doi. 10.1002/tcr.202400067
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- Article
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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- Article
Hypothesis‐Driven Palladium‐Catalyzed Transformations for the Construction of New Molecular Architectures.
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- Chemical Record, 2021, v. 21, n. 12, p. 3470, doi. 10.1002/tcr.202100095
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Allylic Alkylations with Enamine Nucleophiles.
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- Chemical Record, 2016, v. 16, n. 6, p. 2683, doi. 10.1002/tcr.201600071
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- Article
Regiospecific allyl chlorination of betulin and diacetylbetulin.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 2, p. 303, doi. 10.1134/S1070428017020294
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Development of general methods for the synthesis of new substituted allyl bromides as promising alkenylating agents.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 7, p. 953, doi. 10.1134/S1070428014070069
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Vinylic substitution in the reaction of betulin diacetate with tert-butyl hypochlorite.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 1, p. 78, doi. 10.1134/S1070428013010144
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- Article
Catalytic asymmetric Tsuji–Trost α−benzylation reaction of N-unprotected amino acids and benzyl alcohol derivatives.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30277-9
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- Article
Stereoselective Synthesis of the I–L Fragment of the Pacific Ciguatoxins.
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- Toxins, 2020, v. 12, n. 12, p. 740, doi. 10.3390/toxins12120740
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- Article
Nickel‐Catalyzed Allylic Substitution Reactions: An Evolving Alternative.
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- European Journal of Inorganic Chemistry, 2022, v. 2022, n. 2, p. 1, doi. 10.1002/ejic.202100820
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Metallated Container Molecules: A Capsular Nickel Catalyst for Enhanced Butadiene Polymerisation.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 43, p. 4690, doi. 10.1002/ejic.201901074
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β-Pinene and camphor based, pyrazole-tethered triarylphosphines as chiral P,N ligands for palladium.
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- ARKIVOC: Online Journal of Organic Chemistry, 2021, v. 2021, p. 217, doi. 10.24820/ark.5550190.p011.550
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Chiral pyrrolidine thioethers and 2-azanorbornane derivatives bearing additional nitrogen functions. Enantiopure ligands for palladium-catalyzed Tsuji-Trost reaction.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 162, doi. 10.3998/ark.5550190.p009.792
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Access to Polycyclic Alkaloid-Like Structures by Coupling the Passerini and Ugi Reactions with Two Sequential Metal-Catalyzed Cyclizations.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 18, p. 2940, doi. 10.1002/adsc.201600638
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- Article
Catalytic Asymmetric Synthesis of Phosphoryl-1,4-dihydropyridazines via an Enantioselective Allylic Alkylation/1,3-Dipolar Cycloaddition/Rearrangement Reaction Sequence.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 14, p. 2280, doi. 10.1002/adsc.201600353
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- Article
Planar-Chiral Cyclopentadienyl-Ruthenium-Catalyzed Regio- and Enantioselective Asymmetric Allylic Alkylation of Silyl Enolates under Unusually Mild Conditions.
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- Advanced Synthesis & Catalysis, 2016, v. 358, n. 4, p. 555, doi. 10.1002/adsc.201500970
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Improvements and Applications of the Transition Metal-Free Asymmetric Allylic Alkylation using Grignard Reagents and Magnesium Alanates.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 14/15, p. 3171, doi. 10.1002/adsc.201500495
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Regio- and Enantioselective Allylation of Phenols via Decarboxylative Allylic Etherification of Allyl Aryl Carbonates Catalyzed by (Cyclopentadienyl)ruthenium(II) Complexes and Pyridine-Hydrazone Ligands.
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- 2015
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- Other
An Efficient Protocol for the Palladium-Catalyzed Asymmetric Decarboxylative Allylic Alkylation Using Low Palladium Concentrations and a Palladium(II) Precatalyst.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 10, p. 2238, doi. 10.1002/adsc.201500253
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- Article
Palladium-Catalyzed Intramolecular ipso-Friedel-Crafts Allylic Alkylation of Phenols via Arylative Activation of Allenes.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 13, p. 2693, doi. 10.1002/adsc.201300326
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- Article
Iron-Catalyzed Regio- and Stereoselective Conjugate Addition of Aryl-Grignard Reagents to α,β,γ,δ-Unsaturated Sulfones and its Synthetic Application.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 9, p. 1736, doi. 10.1002/adsc.201201124
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Direct Synthesis of Allyl Amines with 2‐Nitrosulfonamide Derivatives via the Tsuji‐Trost Reaction.
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- ChemistryOpen, 2021, v. 10, n. 12, p. 1166, doi. 10.1002/open.202100147
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MMZ-Catalyzed Tsuji-Trost Type of Reaction: A Selective Mono/Bis Allylation of Dicarbonyl Compounds.
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- Catalysis Letters, 2017, v. 147, n. 11, p. 2755, doi. 10.1007/s10562-017-2185-3
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- Article
Asymmetric Allylic Alkylation and Hydrogenation with Transition Metal Complexes of Diphosphite Ligands Based on (1 S,2 S)- Trans-1,2-cyclohexanediol.
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- Catalysis Letters, 2017, v. 147, n. 4, p. 893, doi. 10.1007/s10562-017-1986-8
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- Article
Passerini/Tsuji–Trost Strategy towards Pyrrole Derivatives.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 29, p. 4242, doi. 10.1002/ejoc.201700653
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- Article
Organocatalytic α-Allylation of α-Branched Aldehydes by Synergistic Catalysis of Brønsted Acids and Amines.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 28, p. 4768, doi. 10.1002/ejoc.201600725
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- Article
Complementary Methods for the Introduction of the ( E)-3-(Pentafluorosulfanyl)allyl Chain unto O-, N-, S-, and C-Based Nucleophiles.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 27, p. 4611, doi. 10.1002/ejoc.201600684
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- Article