Works matching DE "ENOLS"
Results: 195
Mechanistic Insights about the Ligand‐Enabled Oxy‐arylation/vinylation of Alkenes via Au(I)/Au(III) Catalysis.
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- Chemistry - A European Journal, 2022, v. 28, n. 60, p. 1, doi. 10.1002/chem.202202110
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An Expedient Method for the Umpolung Coupling of Enols with Heteronucleophiles**.
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- Chemistry - A European Journal, 2022, v. 28, n. 44, p. 1, doi. 10.1002/chem.202201000
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Iterative Synthesis of 2‐Deoxyoligosaccharides Enabled by Stereoselective Visible‐Light‐Promoted Glycosylation.
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- Angewandte Chemie, 2022, v. 134, n. 20, p. 1, doi. 10.1002/ange.202114726
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Enantio‐ and Regioselective Palladium(II)‐Catalyzed Dioxygenation of (Aza‐)Alkenols.
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- Angewandte Chemie, 2021, v. 133, n. 40, p. 21891, doi. 10.1002/ange.202109312
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Enantio‐ and Diastereodivergent Sequential Catalysis Featuring Two Transition‐Metal‐Catalyzed Asymmetric Reactions.
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- Angewandte Chemie, 2021, v. 133, n. 31, p. 17069, doi. 10.1002/ange.202105800
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An Ion‐Pairing Approach to Stereoselective Metal‐Free Ring‐Opening Metathesis Polymerization.
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- Angewandte Chemie, 2021, v. 133, n. 25, p. 14071, doi. 10.1002/ange.202016393
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An Enolate‐Structure‐Enabled Anionic Cascade Cyclization Reaction: Easy Access to Complex Scaffolds with Contiguous Six‐, Five‐, and Four‐Membered Rings.
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- Angewandte Chemie, 2020, v. 132, n. 45, p. 20295, doi. 10.1002/ange.202008317
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Gold(I)/Gold(III) Catalysis that Merges Oxidative Addition and π‐Alkene Activation.
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- Angewandte Chemie, 2020, v. 132, n. 38, p. 16768, doi. 10.1002/ange.202006074
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Surface‐Driven Keto–Enol Tautomerization: Atomistic Insights into Enol Formation and Stabilization Mechanisms.
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- Angewandte Chemie, 2018, v. 130, n. 51, p. 16901, doi. 10.1002/ange.201808453
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DFT, AIM, and NBO analyses of 1-methyl-2-thioxoimidazolidin-4-one tautomers and their complexes with iodine.
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- Journal of Structural Chemistry, 2012, v. 53, n. 4, p. 649, doi. 10.1134/S0022476612040063
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Gas Phase Catalytic Hydrogenation of C4 Alkynols over Pd/Al2O3.
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- Catalysts (2073-4344), 2019, v. 9, n. 11, p. 924, doi. 10.3390/catal9110924
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In search of the dark state of 5-methyl-2-hydroxypyrimidine using a numerical DFT/MRCI gradient.
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- Molecular Physics, 2012, v. 110, n. 19/20, p. 2429, doi. 10.1080/00268976.2012.695030
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Quantum-Chemical Search for Keto Tautomers of Azulenols in Vacuo and Aqueous Solution.
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- Symmetry (20738994), 2021, v. 13, n. 3, p. 497, doi. 10.3390/sym13030497
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Detection of an enol intermediate in the hydroperoxide lyase chain cleavage reaction
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- FEBS Letters, 2003, v. 549, n. 1-3, p. 31, doi. 10.1016/S0014-5793(03)00758-0
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Radical addition to ynol ethers — A convenient procedure for the stereoselective preparation of α-iodo enol ethers in neutral conditions.
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- Canadian Journal of Chemistry, 2008, v. 86, n. 10, p. 970, doi. 10.1139/v08-094
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Generation, observation, and reactivity of furyl- and thienylketenes and bisketenes.
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- Canadian Journal of Chemistry, 2008, v. 86, n. 4, p. 333, doi. 10.1139/V08-021
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Ketonization of the unusually acidic elongated enol generated by flash photolytic decarboxylation of p-formylphenylacetic acid in aqueous solution.
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- Canadian Journal of Chemistry, 2008, v. 86, n. 2, p. 101, doi. 10.1139/V07-095
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In situ nitrosonium ion generation — α-Oximinylation of enol ethers from steroidal spiroketals: Introduction of C23 (R)-OH in cephalostatin intermediates.
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- Canadian Journal of Chemistry, 2006, v. 84, n. 10, p. 1442, doi. 10.1139/V06-113
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The water elimination from the ethyl acetate radical cation — Answers from theory to a longstanding mechanistic problem.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 11, p. 1847, doi. 10.1139/V05-199
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A study of the isomerization and dissociation of formal [acetone–methanol]<sup>+·</sup> ion–molecule complexes.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 11, p. 1903, doi. 10.1139/V05-200
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Acid enol and dihydropyridine intermediates in pyridylketene hydration — A computational study.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 9, p. 1561, doi. 10.1139/V05-162
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The 2-oxo-3,3,5,5-tetramethylcyclopentanecarboxylic acid keto–enol system in aqueous solution — Generation of the enol by flash photolytic Wolff rearrangement of 2-diazo-4,4,6,6-tetramethylcyclohexane-1,3-dione followed by hydration of the acylketene thus formed
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- Canadian Journal of Chemistry, 2005, v. 83, n. 1, p. 68, doi. 10.1139/V04-152
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Nucleophilic additions of lactam-derived enol triflates to aldehydes mediated by nickel(II) and chromium(II) salts.
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- Canadian Journal of Chemistry, 2004, v. 82, n. 2, p. 139, doi. 10.1139/V03-164
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The crystal structure of a simple enol formed in a single-crystal-to-single-crystal enolene rearrangement.
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- Canadian Journal of Chemistry, 2004, v. 82, n. 2, p. 301, doi. 10.1139/V03-207
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Lewis acid-mediated intramolecular addition of silyl enol ethers to internal unactivated alkynes.
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- Canadian Journal of Chemistry, 2001, v. 79, n. 11, p. 1624, doi. 10.1139/v01-134
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Mechanisms and structures of crotonase superfamily enzymes – How nature controls enolate and oxyanion reactivity.
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- Cellular & Molecular Life Sciences, 2008, v. 65, n. 16, p. 2507, doi. 10.1007/s00018-008-8082-6
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Oligomer formation during gas-phase ozonolysis of small alkenes and enol ethers: new evidence for the central role of the Criegee Intermediate as oligomer chain unit.
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- Atmospheric Chemistry & Physics Discussions, 2007, v. 7, n. 5, p. 14041, doi. 10.5194/acpd-7-14041-2007
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Asymmetric synthesis of (S)‐3‐methyleneglutamic acid and its N‐Fmoc derivative via Michael addition–elimination reaction of chiral glycine Ni (II) complex with enol tosylates.
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- Chirality, 2021, v. 33, n. 3, p. 115, doi. 10.1002/chir.23291
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Regio-, stereo-, and enantioselective reactions of carbon acids catalyzed by recoverable organic catalysts bearing ionic liquid moieties.
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- Pure & Applied Chemistry, 2009, v. 81, n. 11, p. 2059, doi. 10.1351/PAC-CON-08-12-05
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An identification of the C–C bonding spin adduct in the spin trapping of N-methyl benzohydroxamic acid radical by 5,5-dimethyl-1-pyrroline N-oxide.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 8, p. 1, doi. 10.1007/s00214-016-1944-3
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Assisted intramolecular proton transfer in (uracil)Ca complexes.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2011, v. 128, n. 4-6, p. 457, doi. 10.1007/s00214-010-0801-z
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A study of amino-protecting groups using the polarizable continuum model (PCM).
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2004, v. 111, n. 2-6, p. 231, doi. 10.1007/s00214-003-0514-7
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Organic chemistry: Overcoming catalytic bias.
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- 2011
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- Opinion
Comparison of Gas-Chromatographic Retention Parameters of Aliphatic Enyne Alcohols with the Data for Their Structural Analogues.
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- Journal of Analytical Chemistry, 2023, v. 78, n. 1, p. 74, doi. 10.1134/S1061934822120139
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A possible salicylideneanilines-based optical molecular switch induced by a reversible hydrogen transfer: an ab initio study.
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- Molecular Physics, 2011, v. 109, n. 2, p. 209, doi. 10.1080/00268976.2010.515255
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Selective Oxidation of Beuzylic and Allylic Alcohols with NaOCl/Silica Gel System.
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- Journal of the Iranian Chemical Society, 2009, v. 6, n. 2, p. 288, doi. 10.1007/BF03245836
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Hidden in the flames.
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- Science Scope, 2006, v. 29, n. 5, p. 8
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Method development and validation for the quantification of organic acids in microbial samples using anionic exchange solid-phase extraction and gas chromatography-mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2020, v. 412, n. 27, p. 7491, doi. 10.1007/s00216-020-02883-3
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Aniline-based catalysts as promising tools to improve analysis of carbonyl compounds through derivatization techniques: preliminary results using dansylacetamidooxyamine derivatization and LC-fluorescence.
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- Analytical & Bioanalytical Chemistry, 2018, v. 410, n. 27, p. 7031, doi. 10.1007/s00216-018-1304-3
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Synthesis of spiroketal enol ethers related to tonghaosu and their insecticidal activities.
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- Pest Management Science, 2005, v. 61, n. 5, p. 477, doi. 10.1002/ps.991
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Facile synthesis and reactions of some olefin-substituted acetylacetonate complexes.
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- Journal of Coordination Chemistry, 2006, v. 59, n. 18, p. 2083, doi. 10.1080/00958970600742957
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SYNTHESIS AND CATIONIC PHOTOPOLYMERIZATION OF OLIGOMERS BEARING TERMINAL AND INTERNAL ENOL ETHER GROUPS.
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- Journal of Macromolecular Science: Pure & Applied Chemistry, 2001, v. 38, n. 5/6, p. 487, doi. 10.1081/MA-100103362
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Stereoselective Synthesis of Polysubstituted Tetrahydropyrans by Br ø nsted Acid‐Mediated Hydroxyalkoxylation of Silylated Alkenols.
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- Asian Journal of Organic Chemistry, 2024, v. 13, n. 7, p. 1, doi. 10.1002/ajoc.202400096
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Thiocyanation/Cyclization of γ‐hydroxy Olefins to Access Thiocyanato‐Containing Oxygen Heterocyclic Compounds.
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- Asian Journal of Organic Chemistry, 2021, v. 10, n. 7, p. 1643, doi. 10.1002/ajoc.202100175
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Selenium-Catalyzed Oxacyclization of Alkenoic Acids and Alkenols.
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- Asian Journal of Organic Chemistry, 2017, v. 6, n. 8, p. 988, doi. 10.1002/ajoc.201700193
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Studying the hydrogen atom position in the strong-short intermolecular hydrogen bond of pure and 5-substituted 9-hydroxyphenalenones by invariom refinement and ONIOM cluster computations.
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- Zeitschrift für Kristallographie. Crystalline Materials, 2020, p. 225, doi. 10.1515/zkri-2020-0022
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Breaking scaling relationships in alkynol semi-hydrogenation by manipulating interstitial atoms in Pd with d-electron gain.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30540-z
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Alkyl Enol Ethers: Development in Intermolecular Organic Transformation.
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- Chemistry - An Asian Journal, 2021, v. 16, n. 13, p. 1685, doi. 10.1002/asia.202100277
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Enantioselective Haloetherifications Catalyzed by 1,1′-Bi-2-naphthol (BINOL) Phosphates: From Symmetrical Alkenediols to Simple Alkenols.
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- Chemistry - An Asian Journal, 2014, v. 9, n. 8, p. 2162, doi. 10.1002/asia.201402229
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Chiral Enol Oxazolines and Thiazolines as Auxiliary Ligands for the.
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- Chemistry - An Asian Journal, 2013, v. 8, n. 9, p. 2274, doi. 10.1002/asia.201300598
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- Article