Works matching DE "STILLE reaction"
Results: 117
Trichalcogenasupersumanenes and its concave-convex supramolecular assembly with fullerenes.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39086-0
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- Article
POLYBINAPHTHYLS INCORPORATING (R)-2,2′-BINAPHTHO-20-CROWN-6 AND NAPHTHYL MOITIES.
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- Chinese Journal of Polymer Science (World Scientific Publishing Company), 2006, v. 24, n. 6, p. 619, doi. 10.1142/S0256767906001722
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Front Cover: Pd‐Catalyzed Sonogashira Cross‐Coupling Reactions of gem‐Dibromovinyl BODIPY Derivatives (22/2021).
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 22, p. 3121, doi. 10.1002/ejoc.202100600
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Chemoselective Access to π-Conjugated Heterocycles by Stille and Sonogashira Reactions on 2-Substituted 4H-Pyrido[ e][1,3]oxazin-4-ones.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 4, p. 827, doi. 10.1002/ejoc.201601338
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A Short and Efficient Approach for the Total Synthesis of ( S)-Zearalenone and ( R)-De- O-methyllasiodiplodin by Using Stille and RCM Protocols.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 9, p. 1684, doi. 10.1002/ejoc.201501545
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- Article
Thiophene- S, S-dioxidized Indophenine: A Quinoid-Type Building Block with High Electron Affinity for Constructing n-Type Polymer Semiconductors with Narrow Band Gaps.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 10, p. 3459, doi. 10.1002/anie.201508781
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Total Synthesis of Ileabethoxazole, Pseudopteroxazole, and seco-Pseudopteroxazole.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 8, p. 2851, doi. 10.1002/anie.201510568
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Functionalization of pyrrolo[2,3- d]pyrimidine by palladium-catalyzed cross-coupling reactions (review).
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- Chemistry of Heterocyclic Compounds, 2012, v. 48, n. 2, p. 258, doi. 10.1007/s10593-012-0986-2
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Synthesis of Novel Key Chromophoric Intermediates via C-C Coupling Reactions.
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- Catalysts (2073-4344), 2022, v. 12, n. 10, p. 1292, doi. 10.3390/catal12101292
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- Article
Improving Photocatalytic Stille Coupling Reaction by CuPd Alloy-Doped Ordered Mesoporous TiO 2.
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- Catalysts (2073-4344), 2022, v. 12, n. 10, p. 1238, doi. 10.3390/catal12101238
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- Article
Dithienopyrrole-/Benzodithiophene-Based Donor-Acceptor Polymers for Memristor.
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- ChemPlusChem, 2014, v. 79, n. 9, p. 1263, doi. 10.1002/cplu.201402133
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Stille Cross-Coupling for the Functionalization of the Imidazole Backbone: Revisit, Improvement, and Applications of the Method.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 16, p. 3506, doi. 10.1002/ejoc.201500328
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- Article
A Facile Route to Bis(pyridyl-1,3,5-triazine) Ligands with Fluorescing Properties.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 11, p. 2366, doi. 10.1002/ejoc.201403521
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Total synthesis of (–)-pateamine A, a novel immunosuppressive agent from Mycale sp.
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- Canadian Journal of Chemistry, 2004, v. 82, n. 2, p. 353, doi. 10.1139/V03-199
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- Article
A one-pot synthesis of (E,E)-1-arylseleno-substituted 1,5-dien-3-ynes by palladium-catalysed three component cross-coupling reaction.
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- Journal of Chemical Research, 2010, v. 34, n. 11, p. 627, doi. 10.3184/030823410X12878393498458
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Synthesis of (E)-α,β-unsaturated ketones by hydrostannylation-Stille tandem reaction of alkylarylacetylenes with acyl chlorides.
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- Journal of Chemical Research, 2010, v. 34, n. 10, p. 559, doi. 10.3184/030823410X12861973220846
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A novel stereoselective synthesis of trisubstituted 1,3-dienes by a hydrostannylation-Stille tandem reaction of alkylarylacetylenes with alkenyl halides.
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- Journal of Chemical Research, 2010, v. 34, n. 3, p. 175, doi. 10.3184/030823410X12680741110954
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Facile Synthesis of Triphenylamine Based Hyperbranched Polymer for Organic Field Effect Transistors.
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- Nanomaterials (2079-4991), 2019, v. 9, n. 12, p. 1787, doi. 10.3390/nano9121787
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Preparation and Characterization of Quinoxaline-Pyrene-Based Conjugated Copolymers for Organic Photovoltaic Devices.
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- Coatings (2079-6412), 2020, v. 10, n. 11, p. 1098, doi. 10.3390/coatings10111098
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Stereoselective Synthesis of Rubrenoic and nor-Rubrenoic acids.
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- Synthetic Communications, 2008, v. 38, n. 1, p. 54, doi. 10.1080/00397910701649049
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- Article
Direct and Improved Access to Unsymmetrically Functionalized Bipyridines by a Stille-Type Cross-Coupling Reaction.
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- Synthetic Communications, 2003, v. 33, n. 3, p. 409, doi. 10.1081/SCC-120015770
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BNPs@Cur-Pd as a versatile and recyclable green nanocatalyst for Suzuki, Heck and Stille coupling reactions.
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- Journal of Experimental Nanoscience, 2020, v. 15, n. 1, p. 182, doi. 10.1080/17458080.2020.1761959
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The Pd(0) nanoparticles stabilized by collagen fibres as a recyclable heterogeneous catalyst for the Stille reaction under aerobic condition.
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- Journal of Chemical Sciences, 2013, v. 125, n. 4, p. 813, doi. 10.1007/s12039-013-0456-0
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Synthesis and Characterization of Soluble Silyl End-capped Arene-Thiophene Co-Oligomers.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 5, p. 1345, doi. 10.1002/bkcs.10257
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Synthesis and Physical Properties of Asymmetrical Quaterthiophene Derivatives as Organic Thin-Film Transistor Materials.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 4, p. 1215, doi. 10.1002/bkcs.10233
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- Article
On the Triple Role of Fluoride Ions in Palladium-Catalyzed Stille Reactions.
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- Chemistry - A European Journal, 2015, v. 21, n. 50, p. 18401, doi. 10.1002/chem.201503309
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Callipeltosides A, B and C: Total Syntheses and Structural Confirmation.
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- Chemistry - A European Journal, 2015, v. 21, n. 38, p. 13261, doi. 10.1002/chem.201501877
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Phosphine-Free Stille-Migita Chemistry for the Mild and Orthogonal Modification of DNA and RNA.
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- Chemistry - A European Journal, 2014, v. 20, n. 50, p. 16613, doi. 10.1002/chem.201404843
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Synthesis of 15-(4-[C]methylphenyl)pentadecanoic acid (MePPA) via Stille cross-coupling reaction.
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- Journal of Radioanalytical & Nuclear Chemistry, 2011, v. 288, n. 3, p. 881, doi. 10.1007/s10967-011-1022-1
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A highly efficient and recyclable Pd(PPh<sub>3</sub>)<sub>4</sub>/PEG-400 system for Stille cross-coupling reactions of organostannanes with aryl bromides.
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- Journal of Chemical Research, 2017, v. 41, n. 9, p. 547, doi. 10.3184/174751917X15045169836226
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- Article
Recent Developments in C–H Activation for Materials Science in the Center for Selective C–H Activation.
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- Molecules, 2018, v. 23, n. 4, p. 922, doi. 10.3390/molecules23040922
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Pd<sup>0</sup>-Catalyzed Methyl Transfer on Nucleosides and Oligonucleotides, Envisaged as a PET Tracer.
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- Molecules, 2013, v. 18, n. 11, p. 13654, doi. 10.3390/molecules181113654
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Carbon-Carbon Cross Coupling Reactions in Ionic Liquids Catalysed by Palladium Metal Nanoparticles.
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- Molecules, 2010, v. 15, n. 5, p. 3421, doi. 10.3390/molecules15053441
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- Article
Thioacetyl-Terminated Ferrocene-Anthraquinone Conjugates: Synthesis, Photo- and Electrochemical Properties Triggered by Protonation-Induced Intramolecular Electron Transfer.
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- Molecules, 2010, v. 15, n. 1, p. 150, doi. 10.3390/molecules15010150
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- Article
Synthesis and evaluation of N-isopropyl-p-[<sup>11</sup>C]methylamphetamine as a novel cerebral blood flow tracer for positron emission tomography.
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- EJNMMI Research, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13550-020-00702-5
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Design and Synthesis of Disk-liked Benzotrithiophene Small Molecules for the Organic Solar Cells Material.
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- Oriental Journal of Chemistry, 2024, v. 40, n. 5, p. 1199, doi. 10.13005/ojc/400501
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- Article
Preparation and electrochemical properties of thieno-[3,4-b] pyrazine conjugated polymer composite supercapacitor carbon powder electrode materials for Li-organic battery.
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- High Performance Polymers, 2023, v. 35, n. 7, p. 686, doi. 10.1177/09540083231163582
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- Article
Cross‐Dehydrogenative Coupling Polymerization via C−H Activation for the Synthesis of Conjugated Polymers.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202301247
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- Article
Modular Access to Diverse Chemiluminescent Dioxetane‐Luminophores through Convergent Synthesis.
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- Angewandte Chemie, 2022, v. 134, n. 22, p. 1, doi. 10.1002/ange.202202187
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- Article
Rücktitelbild: Defect‐Free Alternating Conjugated Polymers Enabled by Room‐ Temperature Stille Polymerization (Angew. Chem. 16/2022).
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- Angewandte Chemie, 2022, v. 134, n. 16, p. 1, doi. 10.1002/ange.202203490
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Defect‐Free Alternating Conjugated Polymers Enabled by Room‐ Temperature Stille Polymerization.
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- Angewandte Chemie, 2022, v. 134, n. 16, p. 1, doi. 10.1002/ange.202115969
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- Article
Mild and Robust Stille Reactions in Water using Parts Per Million Levels of a Triphenylphosphine‐Based Palladacycle.
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- Angewandte Chemie, 2021, v. 133, n. 8, p. 4204, doi. 10.1002/ange.202014141
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- Article
Synthesis of a new family of 2-ethylidene-γ-unsaturated δ-amino esters via microwave activated Stille coupling.
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- Amino Acids, 2010, v. 39, n. 1, p. 175, doi. 10.1007/s00726-009-0392-y
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- Article
Coupling Pyrazine to Dithiocarbonates for Molybdopterin Model Ligands—Indispensable Tin.
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- Inorganics, 2023, v. 11, n. 5, p. 188, doi. 10.3390/inorganics11050188
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- Article
GREEN SYNTHESIS OF 1-METHYL-2-PHENYL-3-(THIOPHEN-2-YL)- 1H-INDOLE.
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- International Journal of Ecosystems & Ecology Sciences, 2021, v. 11, n. 3, p. 667, doi. 10.31407/ijees11.341
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Synthesis and properties of functional dyes with squaraine-naphthalene diimide hybrid structure.
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- Research on Chemical Intermediates, 2018, v. 44, n. 8, p. 4783, doi. 10.1007/s11164-018-3284-5
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- Article
A Review on Synthetic Approaches for Preparation of Donor-Acceptor Conjugated System.
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- Turkish Online Journal of Qualitative Inquiry, 2021, v. 12, n. 8, p. 281
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- Article
α- and β-Lipomycin: Total Syntheses by Sequential Stille Couplings and Assignment of the Absolute Configuration of All Stereogenic Centers.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 28, p. 7328, doi. 10.1002/anie.201402255
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- Article
Stable Alkyne‐Bridged Conjugated Polymer Nanoparticles With a High NIR‐II Photothermal Conversion Efficiency of 71% for Effective Photothermal Tumor Therapy.
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- Macromolecular Chemistry & Physics, 2024, v. 225, n. 24, p. 1, doi. 10.1002/macp.202400300
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- Article
Aggregation‐Induced Emission Near‐Infrared (NIR)‐II‐Conjugated Polymers Coupled With Nonconjugated Segments for NIR‐II Fluorescence Imaging–Guided NIR‐II Photothermal Therapy.
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- Macromolecular Chemistry & Physics, 2024, v. 225, n. 24, p. 1, doi. 10.1002/macp.202400268
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