Works matching Phosphines
Results: 5000
Palladium(II) complexes of bis(phosphine)monooxide and bis(phosphine)monosulphide ligands bearing o-N,N-dimethylanilinyl substituents.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 6/7, p. 546, doi. 10.1139/V05-067
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Copolymerization of sterically demanding phosphine-olefins and 1-hexene.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 11, p. 1620, doi. 10.1139/V09-120
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Reversible decomposition of mono(α-hydroxy)phosphines and their reaction with α,β-unsaturated aldehydes.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 4, p. 582, doi. 10.1139/V09-021
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Synthesis and redox properties of a phosphine-subsituted para-dioxolene and its bimetallic palladium complex.
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- Canadian Journal of Chemistry, 2008, v. 86, n. 10, p. 976, doi. 10.1139/v08-127
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A General Strategy for Increasing the Air Stability of Phosphines Including Primary Phosphines.
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- Chemistry - A European Journal, 2023, v. 29, n. 68, p. 1, doi. 10.1002/chem.202302518
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Synthesis, characterization, and coordination chemistry of phosphines with ethylenedioxythiophene substituents.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 2, p. 150, doi. 10.1139/V05-004
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29 例磷化氢中毒者体内总磷化氢分布以及磷化氢中毒特征 分析.
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- Journal of Forensic Medicine / Fayixue Zazhi, 2022, v. 38, n. 2, p. 254, doi. 10.12116/j.issn.1004-5619.2020.300901
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Polarity and Conformational Analysis of Tri(1-naphthyl)phosphine, Tri(2-naphthyl)phosphine, and Their Chalcogenides.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 8, p. 1245, doi. 10.1134/S1070428021080030
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Secondary Phosphine Sulfide‐Enabled Iridium‐Catalyzed Asymmetric Allylic Substitution.
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- Angewandte Chemie, 2022, v. 134, n. 52, p. 1, doi. 10.1002/ange.202213904
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Electroreduction: A Sustainable and Less Energy‐Intensive Approach Compared to Chemical Reduction for Phosphine Oxide Recycling to Phosphine.
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- ChemElectroChem, 2022, v. 9, n. 10, p. 1, doi. 10.1002/celc.202101658
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Pt−Me bond cleavage in the reactions of dimethylplatinum(II) complexes containing chelating phosphine ligands with organotin(IV) chlorides.
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- Canadian Journal of Chemistry, 2013, v. 91, n. 12, p. 1288, doi. 10.1139/cjc-2013-0338
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Ferrocenyl phosphine–oxazaphospholidine oxide ligands for the Suzuki–Miyaura coupling of hindered aryl bromides and chlorides.
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- Canadian Journal of Chemistry, 2009, v. 87, n. 1, p. 171, doi. 10.1139/V08-113
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Markovnikov hydroformylation catalyzed by ROPAC in the presence of phosphine and phosphine oxide ligands.
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- Journal of Coordination Chemistry, 2016, v. 69, n. 1, p. 12, doi. 10.1080/00958972.2015.1112381
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Stereoselective inverse conjugate addition of nitrogen and carbon nucleophiles to allenyl phosphine oxide. Synthesis of a,ß-unsaturated phosphine oxides.
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- ARKIVOC: Online Journal of Organic Chemistry, 2012, p. 54
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Methoxyphenyl Substituted Bis(picolyl)phosphines and Phosphine Oxides.
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- European Journal of Inorganic Chemistry, 2016, v. 2016, n. 9, p. 1405, doi. 10.1002/ejic.201600032
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Study on the anti-sulfur-poisoning characteristics of platinum-acetylide-phosphine complexes as catalysts for.
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- Applied Organometallic Chemistry, 2014, v. 28, n. 6, p. 454, doi. 10.1002/aoc.3149
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The synthesis of deuteriated tri-tert-butyl phosphine.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2022, v. 65, n. 13, p. 338, doi. 10.1002/jlcr.4001
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Tris(tetramethylguanidinyl)phosphine: The Simplest Non‐ionic Phosphorus Superbase and Strongly Donating Phosphine Ligand.
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- Chemistry - A European Journal, 2022, v. 28, n. 3, p. 1, doi. 10.1002/chem.202104021
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Easy Access to Phosphine‐Borane Building Blocks.
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- Chemistry - A European Journal, 2020, v. 26, n. 68, p. 15944, doi. 10.1002/chem.202002367
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Quantum Chemical Study of the Addition of Secondary Phosphine Chalcogenides to Vinyl Selenides.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 10, p. 1696, doi. 10.1134/S1070428020100048
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Phosphine-Directed CH Borylation Reactions: Facile and Selective Access to Ambiphilic Phosphine Boronate Esters.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 29, p. 7589, doi. 10.1002/anie.201402868
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Spirocyclopropanes and Substituted Furans by Controlling Reactivity of 1,3‐Enynoates: γ‐ and δ‐Addition of Phosphines to Conjugate Acceptors.
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- Chemistry - A European Journal, 2024, v. 30, n. 69, p. 1, doi. 10.1002/chem.202402688
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Thermally Stable P‐Chiral Supramolecular Phosphines, their Self‐Assembly and Implication in Rh‐Catalyzed Asymmetric Hydrogenation.
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- Chemistry - A European Journal, 2024, v. 30, n. 45, p. 1, doi. 10.1002/chem.202401077
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Ligand Centered Reactivity of a Transition Metal Bound Geometrically Constrained Phosphine.
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- Chemistry - A European Journal, 2024, v. 30, n. 26, p. 1, doi. 10.1002/chem.202400624
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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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Sterically Controlled Late‐Stage Functionalization of Bulky Phosphines.
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- Chemistry - A European Journal, 2022, v. 28, n. 51, p. 1, doi. 10.1002/chem.202202074
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Bridging Homogeneous and Heterogeneous Catalysis: Phosphine‐Functionalized Metal‐Organic Frameworks.
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- Angewandte Chemie, 2024, v. 136, n. 12, p. 1, doi. 10.1002/ange.202315075
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Enantioselective Rhodium‐Catalyzed C−H Arylation Enables Direct Synthesis of Atropisomeric Phosphines.
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- Angewandte Chemie, 2024, v. 136, n. 8, p. 1, doi. 10.1002/ange.202316035
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Rücktitelbild: Ligand‐Free Ultrasmall Recyclable Iridium(0) Nanoparticles for Regioselective Aromatic Hydrogenation of Phosphine Oxide Scaffolds: An Easy Access to New Phosphine Ligands (Angew. Chem. 39/2023).
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- Angewandte Chemie, 2023, v. 135, n. 39, p. 1, doi. 10.1002/ange.202312348
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Synthesis of P‐Stereogenic Phosphine Oxides via Nickel‐Catalyzed Asymmetric Cross‐Coupling of Secondary Phosphine Oxides with Alkenyl and Aryl Bromides.
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- Angewandte Chemie, 2023, v. 135, n. 15, p. 1, doi. 10.1002/ange.202300011
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Metal–Organic Frameworks with Zero and Low‐Valent Metal Nodes Connected by Tetratopic Phosphine Ligands.
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- Angewandte Chemie, 2022, v. 134, n. 11, p. 1, doi. 10.1002/ange.202115454
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Palladium/Xiao‐Phos‐Catalyzed Kinetic Resolution of sec‐Phosphine Oxides by P‐Benzylation.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27453, doi. 10.1002/ange.202111957
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Carbene‐Catalyzed Enantioselective Hydrophosphination of α‐Bromoenals to Prepare Phosphine‐Containing Chiral Molecules.
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- Angewandte Chemie, 2021, v. 133, n. 51, p. 26820, doi. 10.1002/ange.202112860
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A Primary Acyl Phosphine Stabilized by a Phosphonium Ylide.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18695, doi. 10.1002/ange.202106846
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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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Efficacy of Phosphine on Different Life Stages of Alphitobius diaperinus and Tenebrio molitor (Coleoptera: Tenebrionidae).
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- Sustainability (2071-1050), 2023, v. 15, n. 3, p. 2131, doi. 10.3390/su15032131
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Phosphorus magnetic shielding tensors for transition-metal compounds containing phosphine, phosphido, and phosphinidene ligands: Insights from computational chemistry.
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- Canadian Journal of Chemistry, 2004, v. 82, n. 1, p. 27, doi. 10.1139/V03-176
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Structural studies of PdCl[sub 2] L[sub 2] complexes with fluorinated phosphines, phosphites, and phosphinites as precursors of benzyl bromide carbonylation catalysts, and and X-ray crystal structure of cis-PdCl[sub 2] [PPh[sub 2] (OEt)][sub 2].
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- Canadian Journal of Chemistry, 2001, v. 79, n. 5/6, p. 752, doi. 10.1139/v01-075
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A clean and simple method for deprotection of phosphines from borane complexes.
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- Pure & Applied Chemistry, 2018, v. 90, n. 1, p. 49, doi. 10.1515/pac-2017-0313
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Resistance of Stored Grain Pests to Phosphine and Its Integrated Management Strategy.
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- Science & Technology of Cereals, Oils & Foods, 2024, v. 32, n. 1, p. 161, doi. 10.16210/j.cnki.1007-7561.2024.01.021
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Transcriptome profiling and in silico docking analysis of phosphine resistance in rice weevil, Sitophilus oryzae (Coleoptera: Curculionidae).
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- Journal of Insect Science, 2023, v. 23, n. 6, p. 1, doi. 10.1093/jisesa/iead110
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Tri(3‐alkoxyl‐3‐oxopropyl) phosphine oxides derived from PH<sub>3</sub> tail gas as a novel phosphorus‐containing plasticizer for polylactide.
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- Polymers for Advanced Technologies, 2023, v. 34, n. 2, p. 676, doi. 10.1002/pat.5919
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Predicting mortality of phosphine-resistant adults of Sitophilus oryzae (L) (Coleoptera: Curculionidae) in relation to changing phosphine concentration.
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- Pest Management Science, 2004, v. 60, n. 7, p. 655, doi. 10.1002/ps.800
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Solvent‐Free Ruthenium‐Catalyzed Direct Coupling of Phosphines and Aryl Chlorides via C−H Activation: An Efficient and Straight Access to Aryl‐Substituted Biarylphosphines.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 5, p. 1113, doi. 10.1002/ajoc.202100161
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Catalytic Oxidation of Phosphine by Aqueous Copper–Ammonia Complexes.
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- Catalysts (2073-4344), 2023, v. 13, n. 2, p. 271, doi. 10.3390/catal13020271
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Quantum‐chemical investigation of the phosphine ligand effects on the structure and electronic properties of a rhenabenzyne complex.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 5, p. 776, doi. 10.1002/jccs.202000288
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Synthesis of Chiral α‐Substituted β‐Aminophosphine Derivatives through Asymmetric Hydrophosphinylation Utilizing Secondary Phosphine Sulfides.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 24, p. 1, doi. 10.1002/asia.202200989
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Reactivity of tris(3-hydroxypropyl)phosphine species towards reduction of hexachloroiridate(IV): a comparison with tris(2-carboxyethyl)phosphine.
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- Journal of Coordination Chemistry, 2024, v. 77, n. 7/8, p. 670, doi. 10.1080/00958972.2024.2313710
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Parameterization of Phosphine Ligands Modified Rh Complexes to Unravel Quantitative Structure‐Activity Relationship and Mechanistic Pathways in Hydroformylation.
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- ChemCatChem, 2022, v. 14, n. 16, p. 1, doi. 10.1002/cctc.202200423
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Study on Effects of Electron Donors on Phosphine Production from Anaerobic Activated Sludge.
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- Water (20734441), 2017, v. 9, n. 8, p. 563, doi. 10.3390/w9080563
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