Works matching DE "ALLYL halides"
Results: 53
Effects of Ionized Cyclodextrin on Decomposition of Allyl Isothiocyanate in Alkaline Solutions.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 2, p. 433, doi. 10.1271/bbb.68.433
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Metal‐Free Decarboxylative Allylation of Oxime Esters under Light Irradiation.
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- Chemistry - A European Journal, 2024, v. 30, n. 43, p. 1, doi. 10.1002/chem.202401494
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A Thioether‐Catalyzed Cross‐Coupling Reaction of Allyl Halides and Arylboronic Acids.
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- Angewandte Chemie, 2022, v. 134, n. 43, p. 1, doi. 10.1002/ange.202211408
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Umpolung of B−H Bonds by Metal–Ligand Cooperation with Cyclopentadienone Iridium Complexes.
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- Angewandte Chemie, 2021, v. 133, n. 6, p. 2880, doi. 10.1002/ange.202011322
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Selective Oxidation of Glycosyl Sulfides to Sulfoxides with Sodium Hypochlorite and Catalyzed by Metalloporphyrins.
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- Journal of Carbohydrate Chemistry, 2010, v. 29, n. 3, p. 142, doi. 10.1080/07328303.2010.483041
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Sorption of the Fumigant 1,3-Dichloropropene on Soil.
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- Journal of Environmental Science & Health. Part B. Pesticides, Food Contaminants & Agricultural Wastes, 2004, v. 39, n. 4, p. 603, doi. 10.1081/PFC-200026821
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New phosphazene-based chain extenders containing allyl and epoxide groups.
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- Designed Monomers & Polymers, 2003, v. 6, n. 3, p. 245, doi. 10.1163/156855503768336261
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Theoretical conformational study of six-membered cyclic allyl epoxides.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2009, v. 122, n. 5/6, p. 245, doi. 10.1007/s00214-009-0508-1
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Phosphomolybdic Heteropolyacid - Catalyst of Allyl β-Iodoethers' Heterocyclization.
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- Petroleum - Gas University of Ploiesti Bulletin, Technical Series, 2008, v. 60, n. 4, p. 199
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Rongalite as a Sulfone Source: Sulfonylation of para‐Quinone Methides and Alkyl/allyl Halides.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 16, p. 1, doi. 10.1002/asia.202200408
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Reactions of Ruthenium Complexes Containing Pentatetraenylidene Ligand.
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- Chemistry - An Asian Journal, 2016, v. 11, n. 21, p. 3072, doi. 10.1002/asia.201601045
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Synthesis of Allyl Allenes through Three-Component.
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- Chemistry - An Asian Journal, 2013, v. 8, n. 7, p. 1404, doi. 10.1002/asia.201300340
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Inhibition by Allyl Sulfides and Crushed Garlic of O<sup>6</sup>-methylguanine Formation in Liver DNA of Dimethylnitrosamine-Treated Rats.
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- Nutrition & Cancer, 2005, v. 51, n. 1, p. 68, doi. 10.1207/s15327914nc5101_10
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One‐Pot Synthesis of N‐Benzyl/Allyl‐N‐phenyl‐2‐benzothiazolamines from 1‐(2‐Iodophenyl)‐3‐phenylthioureas and Benzyl/Allyl Halides.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 6, p. 1, doi. 10.1002/ejoc.202201145
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Synthesis of compounds containing α-aryl quaternary carbon centers.
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- ARKIVOC: Online Journal of Organic Chemistry, 2010, p. 139
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Cover Feature: N‐(aminobenzyliden)phthalimides as a New Redox Mediator Family for the Selective Indirect Reduction of Benzyl or Allyl Halides (ChemCatChem 15/2023).
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- ChemCatChem, 2023, v. 15, n. 15, p. 1, doi. 10.1002/cctc.202300866
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N‐(aminobenzyliden)phthalimides as a New Redox Mediator Family for the Selective Indirect Reduction of Benzyl or Allyl Halides.
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- ChemCatChem, 2023, v. 15, n. 15, p. 1, doi. 10.1002/cctc.202300489
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Asymmetric Synthesis of a Quaternary Carbon Stereogenic Center by Organocatalysis Using a Primary Amino Acid and Its Salt.
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- Chemical Record, 2023, v. 23, n. 7, p. 1, doi. 10.1002/tcr.202200276
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The addition of hydrogen halides to the carbonyl group to give gem-halogenohydrins.
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- Journal of Chemical Research, 2011, v. 35, n. 6, p. 361, doi. 10.3184/174751911X13088402534637
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Heterocycles Based on 1-((Z)-1,4-dibromobut-2-en-2-yl)adamantane.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 3, p. 298, doi. 10.1007/s10593-021-02907-5
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Synthesis of Epoxyisoindolo[1,2- a]isoquinolinium Salts by an Intramolecular [2+4] Cycloaddition Reaction in 2-Allyl-1-furylisoquinolinium Halides.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 5, p. 746, doi. 10.1007/s10593-013-1306-1
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4-hydroxy-2-quinolones 196. synthesis and bromination of 1-allyl-3-(2-hydroxyethyl)-1 h,3 h-quinazoline-2,4-dione.
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- Chemistry of Heterocyclic Compounds, 2011, v. 47, n. 6, p. 731, doi. 10.1007/s10593-011-0827-8
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Indium(I)/CuFe2O4 Reagent for Allylation of Carbonyls and Epoxide Rearranged Carbonyls.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 11, p. 2189, doi. 10.1134/S1070363220110274
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Synthesis of N-allyl- and N-acyl-2-vinylindoline.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 4, p. 672, doi. 10.1134/S1070363214040112
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Synthesis of allyl ethers derived from polyfluorinated alcohols.
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- Russian Journal of General Chemistry, 2007, v. 77, n. 2, p. 317, doi. 10.1134/S1070363207020235
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Early Organic Chemistry in Kyiv: Serhii Mykolayovych Reformatskyi (1860–1934) and his Name Reaction.
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- ChemPlusChem, 2023, v. 88, n. 10, p. 1, doi. 10.1002/cplu.202300224
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Nitrogen Doped Carbon–Silica Based Cu(0) Nanometal Catalyst Enriched with Well-Defined N-moieties: Synthesis and Application in One-Pot Synthesis of 1,4-Disubstituted-1,2,3-triazoles.
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- Catalysis Letters, 2020, v. 150, n. 1, p. 82, doi. 10.1007/s10562-019-02936-y
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A Photoredox Nozaki‐Hiyama Reaction Catalytic in Chromium.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 29, p. 1, doi. 10.1002/ejoc.202200350
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Three‐Component Synthesis of 2‐Substituted Thiobenzoazoles Using Tetramethyl Thiuram Monosulfide (TMTM) as Thiocarbonyl Surrogate.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 43, p. 6770, doi. 10.1002/ejoc.202001214
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Nickel Catalyzed Intermolecular Carbonyl Addition of Aryl Halide.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 45, p. 7483, doi. 10.1002/ejoc.201901367
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Otrzymywanie i modyfikacja biodegradowalnych poliestrów multifunkcjonalnych.
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- Polimery, 2008, v. 53, n. 3, p. 176
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Triflamidation of Allyl-Containing Substances:Unusual Dehydrobromination vs. Intramolecular Heterocyclization.
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- Molecules, 2022, v. 27, n. 20, p. 6910, doi. 10.3390/molecules27206910
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Efficient Synthesis of a New Family of 2,6-Disulfanyl-9-selenabicyclo[3.3.1]nonanes.
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- Molecules, 2021, v. 26, n. 10, p. 2849, doi. 10.3390/molecules26102849
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Asymmetric Dehydrative Allylation Using Soft Ruthenium and Hard Brønsted Acid Combined Catalyst.
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- Chemical Record, 2021, v. 21, n. 6, p. 1385, doi. 10.1002/tcr.202000157
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PHYLOGENY OF <em>CHLOROMONAS</em> (CHLOROPHYCEAE): A STUDY OF 18S RIBOSOMAL RNA GENE SEQUENCES.
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- Journal of Phycology, 1997, v. 33, n. 2, p. 286, doi. 10.1111/j.0022-3646.1997.00286.x
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Copper-Mediated Introduction of the CF<sub>2</sub>PO(OEt)<sub>2</sub> Motif: Scope and Limitations.
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- Chemistry - A European Journal, 2017, v. 23, n. 68, p. 17318, doi. 10.1002/chem.201703542
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Synthesis of Pyrrolo[2,3- d]pyrimidines by Copper-Mediated Carbomagnesiations of N-Sulfonyl Ynamides and Application to the Preparation of Rigidin A and a 7-Azaserotonin Derivative.
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- Chemistry - A European Journal, 2016, v. 22, n. 40, p. 14397, doi. 10.1002/chem.201602519
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Palladium-Catalyzed Three-Component Cascade Reaction: Facial Access to Densely Functionalized Indolizines.
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- Chemistry - A European Journal, 2015, v. 21, n. 19, p. 7057, doi. 10.1002/chem.201500569
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Stereoselective Total Synthesis of Dodoneine.
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- Helvetica Chimica Acta, 2010, v. 93, n. 10, p. 1960, doi. 10.1002/hlca.200900478
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Organozinc reagents from polyfluoroarenes: Preparation and reactions with allyl halides. Synthesis of allylpolyfluoroarenes.
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- Russian Journal of Organic Chemistry, 2008, v. 44, n. 1, p. 95, doi. 10.1134/S1070428008010119
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Stereoselective synthesis of trisubstituted olefins through 2,5-dialkylidenemagnesacyclopentanes.
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- Russian Journal of Organic Chemistry, 2007, v. 43, n. 7, p. 956, doi. 10.1134/S1070428007070020
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Derivatives of 1,1,2,2-tetraaminoethane. Condensation of 1,2-diacetoxy-1,2-bis(ethoxycarbonylamino)ethane and 1-acetoxy-1,2,2-tris(ethoxycarbonylamino)ethane with nitrogen-containing nucleophiles.
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- Russian Journal of Organic Chemistry, 2007, v. 43, n. 2, p. 305, doi. 10.1134/S1070428007020248
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Transformation of carboxylic acid esters into 2-substituted allyl halides through tertiary cyclopropyl sulfonates. Application in the synthesis of (±)-ipsenol and (±)-ipsdienol, components of Ips typographus spark beetle pheromone.
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- Russian Journal of Organic Chemistry, 2006, v. 42, n. 4, p. 491, doi. 10.1134/S1070428006040038
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Implanted mixed ligand Ni complex of phenolic Schiff base and 2, 2' bipyridine on MCM-41 as an efficient catalyst for Suzuki–Miyaura cross-coupling reactions: a greener approach.
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- Research on Chemical Intermediates, 2022, v. 48, n. 9, p. 3701, doi. 10.1007/s11164-022-04786-7
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Simple Analogues of Acyclonucleosides: Synthesis of N‐Substituted Pyrido[3′,2′:4,5]thieno[3,2‐d]pyrimidine Derivatives
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- Synthetic Communications, 2006, v. 36, n. 19, p. 2751, doi. 10.1080/00397910600767181
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In-MEDIATED ALLYLATION OF α-KETO ESTERS WITH ALLYL HALIDES*.
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- Synthetic Communications, 2001, v. 31, n. 20, p. 3189, doi. 10.1081/SCC-100105896
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Asymmetric 1,3-Dipolar Cycloaddition Reaction of Azomethine Imines to Allyl Alcohol.
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- Chemistry Letters, 2008, v. 37, n. 3, p. 13, doi. 10.1246/cl.2008.342
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An Unprecedented Dimerization of 1,2,3-Butatriene Catalyzed by Palladium Complexes.
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- Chemistry Letters, 2004, v. 33, n. 11, p. 1466, doi. 10.1246/cl.2004.1466
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- Article
Influence of Pt–Pd/TS-1 Catalyst Preparation on Epoxidation of Olefins with Hydrogen Peroxide.
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- Catalysis Letters, 2005, v. 103, n. 1/2, p. 161, doi. 10.1007/s10562-005-6526-2
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Transition-metal-free allylation of 2-azaallyls with allyl ethers through polar and radical mechanisms.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24027-6
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