Works matching DE "SULFIDES
Results: 3886
Dication Disulfuranes as Photoactivatable Sources of Radical Organocatalysts.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202419751
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LiLnGeS<sub>4</sub> (Ln=La−Nd): Designing High Performance Infrared Nonlinear Optical Sulfides through "Band Reformation of AGS".
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- Angewandte Chemie, 2025, v. 137, n. 3, p. 1, doi. 10.1002/ange.202415318
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Mapping Sulphide Mineralization in the Hawiah Area Using Transient Electromagnetic Methods.
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- Minerals (2075-163X), 2025, v. 15, n. 2, p. 186, doi. 10.3390/min15020186
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Synthesis and Biological Activity of Thioethers Containing 1,2,4-Oxadiazole Fragment and Their Oxidation Products.
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- Russian Journal of General Chemistry, 2025, v. 95, n. 1, p. 35, doi. 10.1134/S107036322461189X
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SULFIDO, SELENIDO IR ŠVINO JONŲ POVEIKIS δ-AMINOLEVULINO RŪGŠTIES DEHIDRATAZĖS AKTYVUMUI BANDOMŲJŲ GYVŪNŲ KRAUJYJE IN VITRO.
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- Veterinarija ir Zootechnika, 2006, v. 33, n. 55, p. 69
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Chemical Identity of a Rotting Animal-Like Odor Emitted from the Inflorescence of the Titan Arum (Amorphophallus titanum).
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- Bioscience, Biotechnology & Biochemistry, 2010, v. 74, n. 12, p. 2550, doi. 10.1271/bbb.100692
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Communication: First Total Synthesis of 4-Methylthio-3-butenyl Glucosinolate.
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- Bioscience, Biotechnology & Biochemistry, 2009, v. 73, n. 3, p. 785, doi. 10.1271/bbb.80862
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Diallyl Sulfide Content and Antimicrobial Activity against Food-Borne Pathogenic Bacteria of Chives (Allium schoenoprasum).
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 11, p. 2987, doi. 10.1271/bbb.80482
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Structure-Dependent Photodegradation of Carotenoids Accelerated by Dimethyl Tetrasulfide under UVA Irradiation.
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- Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 8, p. 2176, doi. 10.1271/bbb.80251
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Acceleration Effect of Sulfides on Photodegradation of Carotenoids by UVA Irradiation.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 9, p. 1786, doi. 10.1271/bbb.69.1786
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Involvement of Sulfide:Quinone Oxidoreductase in Sulfur Oxidation of an Acidophilic Iron-Oxidizing Bacterium, Acidithiobacillus ferrooxidans NASF-1.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 12, p. 2519, doi. 10.1271/bbb.68.2519
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Tuning the LCST of PNIPAM via Random Oxidation-Sensitive Thioether Functionalities.
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- Macromolecular Chemistry & Physics, 2017, v. 218, n. 9, p. n/a, doi. 10.1002/macp.201600556
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Phosphonate-Containing Polymeric Networks: Swelling in Water Controlled by Metal Ions.
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- Macromolecular Chemistry & Physics, 2015, v. 216, n. 3, p. 314, doi. 10.1002/macp.201400458
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Cu‐Catalyzed [3+1+1] Cascade Cyclization of O‐Acyl Oximes with Sulfur and Silyl Enol Ethers: Rapid Access to Naphthothiazoles.
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- Chemistry - A European Journal, 2024, v. 30, n. 70, p. 1, doi. 10.1002/chem.202402976
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Base‐Stabilized Gallium Sulfides and Selenides Supported by a Bis(oxazolinyl)(phenyl)methanide Ligand.
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- Chemistry - A European Journal, 2024, v. 30, n. 42, p. 1, doi. 10.1002/chem.202401665
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Copper‐Catalyzed Sulfimidation in Aqueous Media: a Fast, Chemoselective and Biomolecule‐Compatible Reaction.
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- Chemistry - A European Journal, 2024, v. 30, n. 14, p. 1, doi. 10.1002/chem.202303939
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A Green Environmental Protection Photocatalytic Molecular Reactor for Aerobic Oxidation of Sulfide to Sulfoxide.
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- Chemistry - A European Journal, 2024, v. 30, n. 12, p. 1, doi. 10.1002/chem.202303725
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Visible‐Light‐Responsive Polyoxometalate@Metal‐Organic Frameworks Involving Ir Metalloligands for Highly Selective Photocatalytic Oxidation of Sulfides to Sulfoxide.
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- Chemistry - A European Journal, 2024, v. 30, n. 10, p. 1, doi. 10.1002/chem.202303401
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Mechanochemical Nickel‐Catalyzed Carbon‐Sulfur Bond Formation between Aryl Iodides and Aromatic Sulfur Surrogates.
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- Chemistry - A European Journal, 2023, v. 29, n. 60, p. 1, doi. 10.1002/chem.202302119
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Base‐Stabilized Phosphinidene Oxide, Imide and Sulfide.
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- Chemistry - A European Journal, 2023, v. 29, n. 59, p. 1, doi. 10.1002/chem.202301842
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Cover Feature: Base‐Stabilized Phosphinidene Oxide, Imide and Sulfide (Chem. Eur. J. 59/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 59, p. 1, doi. 10.1002/chem.202302810
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Sulfide‐Directed Ir‐Catalyzed Vinylic sp<sup>2</sup> and Benzylic sp<sup>3</sup> C−H Activation for the Construction of Sulfur‐Containing Medium‐Ring System.
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- Chemistry - A European Journal, 2023, v. 29, n. 38, p. 1, doi. 10.1002/chem.202300255
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Chemoselective Methionine Labelling of Recombinant Trastuzumab Shows High In Vitro and In Vivo Tumour Targeting.
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- Chemistry - A European Journal, 2023, v. 29, n. 11, p. 1, doi. 10.1002/chem.202202491
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Access to Enantiomerically Pure P‐Stereogenic Primary Aminophosphine Sulfides under Reductive Conditions.
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- Chemistry - A European Journal, 2022, v. 28, n. 72, p. 1, doi. 10.1002/chem.202202608
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Frontispiece: High Performance Bifunctional Electrocatalysts Designed Based on Transition‐Metal Sulfides for Rechargeable Zn–Air Batteries.
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202286761
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High Performance Bifunctional Electrocatalysts Designed Based on Transition‐Metal Sulfides for Rechargeable Zn–Air Batteries.
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- Chemistry - A European Journal, 2022, v. 28, n. 67, p. 1, doi. 10.1002/chem.202202062
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Improving Photocatalytic Performance through the Construction of a Supramolecular Organic Framework.
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- Chemistry - A European Journal, 2022, v. 28, n. 63, p. 1, doi. 10.1002/chem.202202200
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(Na<sub>0.74</sub>Ag<sub>1.26</sub>)BaSnS<sub>4</sub>: A New AgGaS<sub>2</sub>‐Type Nonlinear Optical Sulfide with a Wide Band Gap and High Laser Induced Damage Threshold.
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- Chemistry - A European Journal, 2022, v. 28, n. 61, p. 1, doi. 10.1002/chem.202202063
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Reactivity of Primary Phosphines and Primary Phosphine Sulfides towards Imines.
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- Chemistry - A European Journal, 2022, v. 28, n. 52, p. 1, doi. 10.1002/chem.202201565
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The Aryl Sulfide Synthesis via Sulfide Transfer.
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- Chemistry - A European Journal, 2022, v. 28, n. 35, p. 1, doi. 10.1002/chem.202200869
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Cu(I)/Chiral Bisoxazoline‐Catalyzed Enantioselective Doyle‐Kirmse Reaction of Allenyl Sulfides with α‐Diazoesters.
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- Chemistry - A European Journal, 2022, v. 28, n. 21, p. 1, doi. 10.1002/chem.202200170
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α‐Functionalisation of Cyclic Sulfides Enabled by Lithiation Trapping.
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- Angewandte Chemie, 2024, v. 136, n. 2, p. 1, doi. 10.1002/ange.202314423
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Gallium Sulfide Quantum Dots with Zinc Sulfide and Alumina Shells Showing Efficient Deep Blue Emission.
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- Angewandte Chemie, 2023, v. 135, n. 45, p. 1, doi. 10.1002/ange.202311317
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Frontispiz: An Efficient Direct Arylation Polycondensation via C−S Bond Cleavage.
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- Angewandte Chemie, 2023, v. 135, n. 41, p. 1, doi. 10.1002/ange.202384161
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Electroreductive Desulfurative Transformations with Thioethers as Alkyl Radical Precursors.
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- Angewandte Chemie, 2023, v. 135, n. 39, p. 1, doi. 10.1002/ange.202304272
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Thioethers as Dichotomous Electrophiles for Site‐Selective Silylation via C−S Bond Cleavage.
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- Angewandte Chemie, 2023, v. 135, n. 25, p. 1, doi. 10.1002/ange.202303470
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Reducing Overpotential of Solid‐State Sulfide Conversion in Potassium‐Sulfur Batteries.
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- Angewandte Chemie, 2023, v. 135, n. 22, p. 1, doi. 10.1002/ange.202301681
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Katalysatorkontrolle über dreifache Stereogenität: Selektive Synthese atropisomerer Sulfone mit stereogenen C−S‐Achsen.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202302084
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Selective CO<sub>2</sub>‐to‐C<sub>2</sub>H<sub>4</sub> Photoconversion Enabled by Oxygen‐Mediated Triatomic Sites in Partially Oxidized Bimetallic Sulfide.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202301075
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Na<sub>2</sub>Ba[Na<sub>2</sub>Sn<sub>2</sub>S<sub>7</sub>]: Structural Tolerance Factor‐Guided NLO Performance Improvement.
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- Angewandte Chemie, 2023, v. 135, n. 7, p. 1, doi. 10.1002/ange.202218048
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In situ Quenchreaktionen von enantiomerenangereicherten sekundären Alkyllithiumreagenzien im Kolben und im kontinuierlichen Durchfluss mittels eines I/Li‐Austausch.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202214377
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Intramolecular Thiol‐ and Selenol‐Assisted Delivery of Hydrogen Sulfide.
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- Angewandte Chemie, 2022, v. 134, n. 45, p. 1, doi. 10.1002/ange.202210754
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Atroposelective Electrophilic Sulfenylation of N‐Aryl Aminoquinone Derivatives Catalyzed by Chiral SPINOL‐Derived Sulfide.
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- Angewandte Chemie, 2022, v. 134, n. 42, p. 1, doi. 10.1002/ange.202211782
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The Synthetic Potential of Thiophenium Ylide Cycloadducts**.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202205963
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Frontispiz: Commonly Used Alkylating Agents Limit Persulfide Detection by Converting Protein Persulfides into Thioethers.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202203684
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Commonly Used Alkylating Agents Limit Persulfide Detection by Converting Protein Persulfides into Thioethers.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202203684
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Photoinduced Chemo‐, Site‐ and Stereoselective α‐C(sp<sup>3</sup>)−H Functionalization of Sulfides.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202203374
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Development of High‐Energy Anodes for All‐Solid‐State Lithium Batteries Based on Sulfide Electrolytes.
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- Angewandte Chemie, 2022, v. 134, n. 25, p. 1, doi. 10.1002/ange.202201249
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Titelbild: Prodrugs of Persulfide and Sulfide: Is There a Pharmacological Difference between the Two in the Context of Rapid Exchanges among Various Sulfur Species In Vivo? (Angew. Chem. 20/2022).
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- Angewandte Chemie, 2022, v. 134, n. 20, p. 1, doi. 10.1002/ange.202201668
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Prodrugs of Persulfide and Sulfide: Is There a Pharmacological Difference between the Two in the Context of Rapid Exchanges among Various Sulfur Species In Vivo?
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- Angewandte Chemie, 2022, v. 134, n. 20, p. 1, doi. 10.1002/ange.202201668
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