Works matching DE "SONOGASHIRA reaction"
Results: 562
Palladium‐Catalyzed Polymerization of Perfluoroalkyl Iodide and Aromatic Alkynes for the Synthesis of Perfluoroalkylated Poly(enyne)s.
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- Macromolecular Chemistry & Physics, 2023, v. 224, n. 1, p. 1, doi. 10.1002/macp.202200274
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Branched Oligophenylenes with Phenylene–Ethynylene Fragments as Anode Interfacial Layer for Solution Processed Optoelectronics.
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- Macromolecular Chemistry & Physics, 2019, v. 220, n. 13, p. N.PAG, doi. 10.1002/macp.201900036
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Superhydrophobic and Flexible Microporous Polymer Paper.
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- Macromolecular Chemistry & Physics, 2017, v. 218, n. 20, p. n/a, doi. 10.1002/macp.201700219
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Glycerol as Reaction Medium for Sonogashira Couplings: A Green Approach for the Synthesis of New Triarylamine‐Based Materials with Potential Application in Optoelectronics.
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- Chemistry - A European Journal, 2024, v. 30, n. 68, p. 1, doi. 10.1002/chem.202402901
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Glyco‐DNA: Enzymatic Synthesis of Base‐Modified and Hypermodified DNA Displaying up to Four Different Monosaccharide Units in the Major Groove.
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- Chemistry - A European Journal, 2024, v. 30, n. 48, p. 1, doi. 10.1002/chem.202402318
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Design and Asymmetric Control of Orientational Chirality by Using the Combination of C(sp<sup>2</sup>)‐C(sp) Levers and Achiral N‐Protecting Group.
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- Chemistry - A European Journal, 2024, v. 30, n. 28, p. 1, doi. 10.1002/chem.202400005
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Pd(0)‐Catalyzed Asymmetric Intramolecular Grignard‐Type Reaction of Vinyl Iodide‐Carbonyl.
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- Chemistry - A European Journal, 2024, v. 30, n. 25, p. 1, doi. 10.1002/chem.202400236
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A Nitronyl Nitroxide‐Substituted Benzotriazinyl Tetraradical.
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- Chemistry - A European Journal, 2024, v. 30, n. 8, p. 1, doi. 10.1002/chem.202303456
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Atroposelective Ni<sup>II</sup>‐Catalyzed Cross‐Coupling Reactions Enable a Deeper Understanding of Negishi Couplings: Isolation and Application of Solid Aryl Higher‐Order Zincates.
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- Chemistry - A European Journal, 2023, v. 29, n. 67, p. 1, doi. 10.1002/chem.202302841
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Synthesis of Bisubstrate Analogues for RNA Methylation Studies using two Transition‐Metal‐Catalyzed Reactions.
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- Chemistry - A European Journal, 2023, v. 29, n. 44, p. 1, doi. 10.1002/chem.202301134
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Micelle‐Mediated Sonogashira Coupling for DNA‐Encoded Library Synthesis.
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- Chemistry - A European Journal, 2023, v. 29, n. 42, p. 1, doi. 10.1002/chem.202300603
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Trinuclear Pd<sup>II</sup> Complexes with a C<sub>3</sub>‐Symmetric Triethynylbenzene‐Based Tris‐NHC Ligand: Catalytic Benefits.
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- Chemistry - A European Journal, 2023, v. 29, n. 39, p. 1, doi. 10.1002/chem.202300548
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Structural and Synthetic Insights on Oxidative Homocouplings of Alkynes Mediated by Alkali‐Metal Manganates.
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- Chemistry - A European Journal, 2023, v. 29, n. 33, p. 1, doi. 10.1002/chem.202300593
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One-Pot Tandem Coupling Method for the Short-Step Formal Synthesis of Riccardin C.
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- Chemistry - A European Journal, 2023, v. 29, n. 16, p. 1, doi. 10.1002/chem.202203805
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Total Synthesis, Absolute Configuration, and Phytotoxic Activity of Foeniculoxin.
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- Chemistry - A European Journal, 2023, v. 29, n. 8, p. 1, doi. 10.1002/chem.202203396
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Copper‐Catalyzed Stereoselective Borylation and Palladium‐Catalyzed Stereospecific Cross‐Coupling to Give Aryl C‐Glycosides.
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- Chemistry - A European Journal, 2023, v. 29, n. 6, p. 1, doi. 10.1002/chem.202203376
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A Cascade Sonogashira Cross‐Coupling‐Substitution‐Elimination Reaction for the Synthesis of Linear Conjugated Dienynes.
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- Chemistry - A European Journal, 2022, v. 28, n. 71, p. 1, doi. 10.1002/chem.202202421
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New Approaches toward Building C<sub>sp</sub>−P bond: A Two‐Decade Overview.
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- Chemistry - A European Journal, 2022, v. 28, n. 50, p. 1, doi. 10.1002/chem.202200957
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Solvent‐Free Synthesis of Core‐Functionalised Naphthalene Diimides by Using a Vibratory Ball Mill: Suzuki, Sonogashira and Buchwald–Hartwig Reactions.
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- Chemistry - A European Journal, 2022, v. 28, n. 49, p. 1, doi. 10.1002/chem.202201444
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Near‐IR Intramolecular Charge Transfer in Strongly Interacting Diphenothiazene‐TCBD and Diphenothiazene‐DCNQ Push‐Pull Triads.
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- Chemistry - A European Journal, 2022, v. 28, n. 25, p. 1, doi. 10.1002/chem.202200348
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Synergistic Palladium/Copper‐Catalyzed 1,4‐Difunctionalization of 1,3‐Dienes for Stereodivergent Construction of 1,5‐Nonadjacent Stereocenters.
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- Angewandte Chemie, 2024, v. 136, n. 21, p. 1, doi. 10.1002/ange.202402843
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Highly Selective Acetylene‐to‐Ethylene Electroreduction Over Cd‐Decorated Cu Catalyst with Efficiently Inhibited Carbon‐Carbon Coupling.
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- Angewandte Chemie, 2024, v. 136, n. 19, p. 1, doi. 10.1002/ange.202400122
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Photocatalytic Terminal C−C Coupling Reaction Inside Water Soluble Nanocages.
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- Angewandte Chemie, 2023, v. 135, n. 45, p. 1, doi. 10.1002/ange.202312500
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Controlled Partial Linker Thermolysis in Metal‐Organic Framework UiO‐66‐NH<sub>2</sub> to Give a Single‐Site Copper Photocatalyst for the Functionalization of Terminal Alkynes.
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- Angewandte Chemie, 2023, v. 135, n. 36, p. 1, doi. 10.1002/ange.202308651
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Dimeric Manganese‐Catalyzed Hydroalkenylation of Alkynes with a Versatile Silicon‐Based Directing Group.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202306922
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Atomically Precise Defective Copper Nanocluster Catalysts for Highly Selective C−C Cross‐Coupling Reactions.
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- Angewandte Chemie, 2023, v. 135, n. 26, p. 1, doi. 10.1002/ange.202303572
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Transition‐Metal‐Free Difunctionalization of Sulfur Nucleophiles**.
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- Angewandte Chemie, 2023, v. 135, n. 8, p. 1, doi. 10.1002/ange.202216296
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Sustainable Wacker‐Type Oxidations.
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- Angewandte Chemie, 2022, v. 134, n. 50, p. 1, doi. 10.1002/ange.202211016
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Highly Regioselective Cobalt‐Catalyzed Hydroboration of Internal Alkynes.
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- Angewandte Chemie, 2022, v. 134, n. 36, p. 1, doi. 10.1002/ange.202208473
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Regioselective Fluoroalkylphosphorylation of Unactivated Alkenes by Radical‐Mediated Alkoxyphosphine Rearrangement**.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202203398
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Metal‐Free C−H Functionalization via Diaryliodonium Salts with a Chemically Robust Dummy Ligand.
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- Angewandte Chemie, 2022, v. 134, n. 28, p. 1, doi. 10.1002/ange.202201240
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Surface‐Plasmon‐Enhanced Transmetalation between Copper and Palladium Nanoparticle Catalyst.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202203158
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Reductant‐Free Cross‐Electrophile Synthesis of Di(hetero)arylmethanes by Palladium‐Catalyzed Desulfinative C−C Coupling.
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- Angewandte Chemie, 2022, v. 134, n. 19, p. 1, doi. 10.1002/ange.202116775
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Joongho Moon.
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- Angewandte Chemie, 2022, v. 134, n. 12, p. 1, doi. 10.1002/ange.202200867
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Enabling the Use of Alkyl Thianthrenium Salts in Cross‐Coupling Reactions by Copper Catalysis.
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- Angewandte Chemie, 2021, v. 133, n. 40, p. 21924, doi. 10.1002/ange.202109723
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Cobalt‐Catalyzed One‐Pot Asymmetric Difunctionalization of Alkynes to Access Chiral gem‐(Borylsilyl)alkanes.
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- Angewandte Chemie, 2021, v. 133, n. 38, p. 20852, doi. 10.1002/ange.202107405
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Sequential Pd<sup>0</sup>‐ and Pd<sup>II</sup>‐Catalyzed Cyclizations: Enantioselective Heck and Nucleopalladation Reactions.
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- Angewandte Chemie, 2021, v. 133, n. 37, p. 20393, doi. 10.1002/ange.202106518
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Graphdiyne:Structure of Fluorescent Quantum Dots.
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- Angewandte Chemie, 2020, v. 132, n. 38, p. 16855, doi. 10.1002/ange.202006891
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Copper‐Catalyzed Enantioselective Sonogashira Type Coupling of Alkynes with α‐Bromoamides.
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- Angewandte Chemie, 2020, v. 132, n. 33, p. 14102, doi. 10.1002/ange.202000860
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Enantioselective Difunctionalization of Alkenes by a Palladium‐Catalyzed Heck/Sonogashira Sequence.
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- Angewandte Chemie, 2020, v. 132, n. 7, p. 2791, doi. 10.1002/ange.201913367
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Pd/Cu‐Catalyzed Enantioselective Sequential Heck/Sonogashira Coupling: Asymmetric Synthesis of Oxindoles Containing Trifluoromethylated Quaternary Stereogenic Centers.
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- Angewandte Chemie, 2020, v. 132, n. 7, p. 2786, doi. 10.1002/ange.201913148
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Self‐Generation of Surface Roughness by Low‐Surface‐Energy Alkyl Chains for Highly Stable Superhydrophobic/Superoleophilic MOFs with Multiple Functionalities.
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- Angewandte Chemie, 2019, v. 131, n. 47, p. 17189, doi. 10.1002/ange.201909912
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Conjugated microporous polymer-based carbazole derivatives as fluorescence chemosensors for picronitric acid.
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- Journal of Materials Science, 2016, v. 51, n. 8, p. 4104, doi. 10.1007/s10853-016-9732-y
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Novel thieno[3,4-c]pyrrole-4,6-dione-based conjugated copolymers with donor-acceptor structures.
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- Journal of Materials Science, 2012, v. 47, n. 1, p. 323, doi. 10.1007/s10853-011-5801-4
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有机麟配体对耙分子偶联催化剂活性的影响.
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- Precious Metals / Guijinshu, 2022, v. 43, n. 1, p. 16
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Reactivity of the 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-ones in a palladium catalyzed Sonogashira cross-coupling reaction.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 6, p. 1216, doi. 10.3906/kim-1505-42
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Copper-free Sonogashira cross-coupling reactions catalyzed by an efficient dimeric C,N-palladacycle in DMF/H<sub>2</sub>O.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 6, p. 1199, doi. 10.3906/kim-1502-86
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Sonogashira reactions for the synthesis of polarized pentacene derivatives.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 6, p. 1180, doi. 10.3906/kim-1505-117
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Palladium nanoparticles supported on modified polystyrene resin as a polymeric catalyst for Sonogashira--Hagihara coupling reactions.
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- Turkish Journal of Chemistry, 2015, v. 39, n. 4, p. 880, doi. 10.3906/kim-1407-22
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Palladium Nanoparticles Supported on Smopex-234 ® as Valuable Catalysts for the Synthesis of Heterocycles.
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- Catalysts (2073-4344), 2021, v. 11, n. 6, p. 706, doi. 10.3390/catal11060706
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