Works matching DE "VINYL halides"
Results: 43
Regioselective Synthesis of New [1,3]Thiazolo- and [1,3]Selenazolo[3,2-a]pyridinium Derivatives.
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- Russian Journal of General Chemistry, 2023, v. 93, p. S87, doi. 10.1134/S1070363223140360
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Assembling of Thiazolo[3,2-a]pyridinium Salts via the Reaction of 2-Pyridinesulfenyl Halides with Vinyl Ethyl Ether.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 12, p. 2601, doi. 10.1134/S1070363219120429
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Acyl Sonogashira Cross-Coupling: State of the Art and Application to the Synthesis of Heterocyclic Compounds.
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- Catalysts (2073-4344), 2020, v. 10, n. 1, p. 25, doi. 10.3390/catal10010025
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Interspecies Competitive Effects in Reduction of Organohalides in Connelly Iron Columns.
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- Environmental Engineering Science, 2006, v. 23, n. 5, p. 874, doi. 10.1089/ees.2006.23.874
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- Article
Palladium-Catalyzed Completely Linear-Selective Negishi Cross-Coupling of Allylzinc Halides with Aryl and Vinyl Electrophiles.
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- Angewandte Chemie, 2013, v. 125, n. 52, p. 14348, doi. 10.1002/ange.201308585
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Stille and Suzuki Cross-Coupling Reactions as Versatile Tools for Modifications at C-17 of Steroidal Skeletons - A Comprehensive Study.
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- Advanced Synthesis & Catalysis, 2017, v. 359, n. 5, p. 832, doi. 10.1002/adsc.201601289
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Nickel-Copper-Catalyzed C(sp²)-N Cross-Coupling of Cyclic and Bridged Amides: An Access to Cyclic Enamides and Alkenyl Vince Lactams.
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- Advanced Synthesis & Catalysis, 2015, v. 357, n. 16/17, p. 3617, doi. 10.1002/adsc.201500457
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Kinetics and Mechanism of Decomposition of the β-Chlorovinyl and β-Iodovinyl Complexes of Platinum(IV) in Aqueous Iodide Solutions.
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- Kinetics & Catalysis, 2004, v. 45, n. 4, p. 478, doi. 10.1023/B:KICA.0000038073.72093.9f
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Synthesis of [ m.n]Cyclophanes: Regiochemistry Transfer from Vinyl Halides to Cyclophanes via Fischer Carbene Complexes.
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- Chemistry - A European Journal, 2013, v. 19, n. 25, p. 8261, doi. 10.1002/chem.201204434
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Copper-catalysed regio- and stereoselective addition of N-heterocycles to gem-dihalo-olefins: synthesis of useful N-vinyl halides.
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- Journal of Chemical Research, 2013, v. 37, n. 9, p. 570, doi. 10.3184/174751913X13756264393878
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Dualism of Ion-Pairing Effects in Nucleophilic Vinylic Substitution with Transition-Metal Carbonyl Anions.
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- ChemPlusChem, 2013, v. 78, n. 9, p. 1190, doi. 10.1002/cplu.201300171
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An Approach Toward the Bridged 14-Membered Carbon Macrocycle of Bielschowskysin.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 16, p. 2793, doi. 10.1002/ejoc.201600271
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Regio- and Stereoselective Synthesis of Vicinal ( Z)-Dihaloalkenylsilanes from Silyl Ethynylarenes.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 5, p. 938, doi. 10.1002/ejoc.201403450
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Synthesis of Vinyl- and Aryl-Acyl Sulfonimidamides Through Pd-Catalyzed Carbonylation Using Mo(CO)<sub>6</sub> as ex situ CO Source.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 1, p. 213, doi. 10.1002/ejoc.201403148
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Transition-Metal-Free Synthesis of ( E)-Vinyl Sulfones from Vinyl Halides in Water.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 31, p. 7050, doi. 10.1002/ejoc.201301101
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Effect of core–shell structures of acrylonitrile–styrene–acrylate (ASA) terpolymer on the properties of poly(vinyl chloride) (PVC)/ASA blends: Miscibility, toughness, and heat resistance.
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- Journal of Applied Polymer Science, 2018, v. 135, n. 43, p. N.PAG, doi. 10.1002/app.46839
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Shielding of Peroxidase Heme Vinyl Groups from Autocatalytically Generated Electrophilic Metabolites.
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- Acta Chimica Slovenica, 2008, v. 55, n. 1, p. 75
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Cross‐Coupling of Sodium Sulfinates with Aryl, Heteroaryl, and Vinyl Halides by Nickel/Photoredox Dual Catalysis.
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- Angewandte Chemie, 2018, v. 130, n. 5, p. 1385, doi. 10.1002/ange.201711104
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Stereodivergent Olefination of Enantioenriched Boronic Esters.
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- Angewandte Chemie, 2017, v. 129, n. 3, p. 804, doi. 10.1002/ange.201610387
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Preparation of Vinyl Arenes by Nickel-Catalyzed Reductive Coupling of Aryl Halides with Vinyl Bromides.
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- Angewandte Chemie, 2016, v. 128, n. 50, p. 15773, doi. 10.1002/ange.201607959
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Synergistic Steric Effects in the Development of a Palladium-Catalyzed Alkyne Carbohalogenation: Stereodivergent Synthesis of Vinyl Halides.
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- Angewandte Chemie, 2015, v. 127, n. 1, p. 256, doi. 10.1002/ange.201409248
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Access to Sulfides through Free Radical Reaction of Vinyl Halides with Thiols.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 1, p. 161, doi. 10.1002/ajoc.201800575
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Nucleophilicity of metal carbonyl anions in vinylic substitution reactions.
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- Journal of Physical Organic Chemistry, 2008, v. 21, n. 3, p. 198, doi. 10.1002/poc.1279
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Advances and New Variations of the Hirao Reaction.
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- Organic Preparations & Procedures International, 2014, v. 46, n. 4, p. 281, doi. 10.1080/00304948.2014.922376
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Stereoselective Synthesis of C‐Vinyl Glycosides via Nickel‐Catalyzed Cross‐Electrophile Couplings of 1,2‐Glycosyl Orthoesters and Vinyl Halides.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 23, p. 3029, doi. 10.1002/cjoc.202400651
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Stereodivergent Olefination of Enantioenriched Boronic Esters.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 3, p. 786, doi. 10.1002/anie.201610387
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Nickel-Catalyzed Intramolecular C−O Bond Formation: Synthesis of Cyclic Enol Ethers.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 26, p. 7437, doi. 10.1002/anie.201601991
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Synergistic Steric Effects in the Development of a Palladium-Catalyzed Alkyne Carbohalogenation: Stereodivergent Synthesis of Vinyl Halides.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 1, p. 254, doi. 10.1002/anie.201409248
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Microscale Preparation of Isotopically Enriched 37ClHC[dbnd]CHF.
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- Synthetic Communications, 2004, v. 34, n. 7, p. 1229, doi. 10.1081/SCC-120030310
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Palladium Catalyzed Synthesis of Phenylquinoxaline-Alkyne Derivatives via Sonogashira Cross Coupling Reaction.
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- Journal of the Chemical Society of Pakistan, 2021, v. 43, n. 1, p. 95, doi. 10.52568/000009
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Halogenophilic and classical Ad E mechanisms in nucleophilic vinylic substitution reactions involving the anions of transition metal carbonyls.
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- Theoretical & Experimental Chemistry, 2011, v. 46, n. 6, p. 350, doi. 10.1007/s11237-011-9165-2
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Synthesis and application of environmental soybean oil-based epoxidized glycidyl ester plasticizer for poly(vinyl chloride).
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- European Journal of Lipid Science & Technology, 2017, v. 119, n. 5, p. n/a, doi. 10.1002/ejlt.201600216
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Gold‐Catalyzed Highly Chemo‐ and Regioselective C‐H Bond Functionalization of Phenols with Haloalkynes.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 24, p. 3867, doi. 10.1002/ejoc.201900653
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- Article
Halogenated Allyl Alcohol Derivatives ‐ Versatile Electrophiles for Palladium‐Catalyzed Allylic Alkylations.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 17, p. 2843, doi. 10.1002/ejoc.201900310
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Isolable Si=B Analogue of a Vinyl Halide: A Building Block for Facile Access toward Silicon‐Boron Multiple Bonded Species.
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- Angewandte Chemie, 2024, v. 136, n. 47, p. 1, doi. 10.1002/ange.202411283
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Asymmetric Construction of an Aryl‐Alkene Axis by Palladium‐Catalyzed Suzuki–Miyaura Coupling Reaction.
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- Angewandte Chemie, 2022, v. 134, n. 45, p. 1, doi. 10.1002/ange.202211211
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First example of the synthesis of N-vinylpyrrole from methoxy- allene and methoxyethyl isothio- cyanate: unprecedented elimination of methanol from a β-substituted methyl ethyl ether.
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- Chemistry of Heterocyclic Compounds, 2010, v. 46, n. 1, p. 61, doi. 10.1007/s10593-010-0470-9
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SIMULATION OF VINYL CHLORIDE PROCESS BY STEADY STATE SEQUENTIAL MODULAR APPROACH - A TEACHING TOOL.
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- i-Manager's Journal on Future Engineering & Technology, 2014, v. 10, n. 2, p. 38
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- Article
Pd‐Catalyzed Negishi Cross‐Coupling of Vinyl Bromides with Diborylmethylzinc Chloride.
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- Bulletin of the Korean Chemical Society, 2021, v. 42, n. 3, p. 499, doi. 10.1002/bkcs.12212
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Palladium-catalyzed Intramolecular Coupling Reactions between Vinyl Bromides, Aryl and Vinyl Halides, and Aryl Iodides Mediated by Indium: Preparation of Five- to Eight-membered Carbocycles and Heterocycles.
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- Bulletin of the Korean Chemical Society, 2015, v. 36, n. 2, p. 711, doi. 10.1002/bkcs.10106
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Contrasting growth properties of <italic>Nocardioides</italic> JS614 on threedifferent vinyl halides.
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- Applied Microbiology & Biotechnology, 2018, v. 102, n. 4, p. 1859, doi. 10.1007/s00253-017-8723-5
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Kinetics of thermal gas-phase decomposition of 2-bromopropene using static system.
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- International Journal of Chemical Kinetics, 2007, v. 39, n. 1, p. 1, doi. 10.1002/kin.20207
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- Article
Aryldiazonium Salts and DABSO: A Versatile Combination for Three‐Component Sulfonylative Cross‐Coupling Reactions.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 11, p. 1, doi. 10.1002/asia.202200085
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