Works matching DE "BECKMANN rearrangement"
Results: 128
Helically Chiral π‐Expanded Azocines Through Regioselective Beckmann Rearrangement and Their Charged States.
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- Angewandte Chemie, 2024, v. 136, n. 29, p. 1, doi. 10.1002/ange.202405570
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Phosphoric Acid‐Catalyzed Enantioselective Synthesis of Axially Chiral Anthrone‐based Compounds.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202213914
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Mark Levin.
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- Angewandte Chemie, 2022, v. 134, n. 51, p. 1, doi. 10.1002/ange.202215042
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Probing the Design Rationale of a High‐Performing Faujasitic Zeotype Engineered to have Hierarchical Porosity and Moderated Acidity.
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- Angewandte Chemie, 2020, v. 132, n. 44, p. 19729, doi. 10.1002/ange.202005108
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Gas-phase Beckmann rearrangement of cyclododecanone oxime on Al,B-MCM-41 mesoporous materials.
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- Journal of Materials Science, 2009, v. 44, n. 24, p. 6741, doi. 10.1007/s10853-009-3601-x
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In situ Generation of Cyclohexanone Drives Electrocatalytic Upgrading of Phenol to Nylon‐6 Precursor.
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- Angewandte Chemie, 2024, v. 136, n. 46, p. 1, doi. 10.1002/ange.202410972
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Synthesis of Long‐Chain Polyamides via Main‐Chain Modification of Polyethyleneketones.
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- Angewandte Chemie, 2024, v. 136, n. 43, p. 1, doi. 10.1002/ange.202410849
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The Beckmann rearrangement in the framework of reaction electronic flux.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2017, v. 136, n. 1, p. 1, doi. 10.1007/s00214-016-2025-3
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Hierarchical SAPO‐34 Architectures with Tailored Acid Sites using Sustainable Sugar Templates.
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- ChemistryOpen, 2018, v. 7, n. 4, p. 297, doi. 10.1002/open.201800001
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Upcycling polyethylene into closed-loop recyclable polymers through titanosilicate catalyzed C-H oxidation and in-chain heteroatom insertion.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-53506-9
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SYNTHESIS OF 1,1,2-TRISUBSTITUTED CYCLOPROPANE RING THROUGH CARBON-CARBON BOND NUCLEOPHILE-INTERCEPTED BECKMANN FRAGMENTATION REACTION.
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- Rasayan Journal of Chemistry, 2020, v. 13, n. 4, p. 2352, doi. 10.31788/RJC.2020.1345745
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CITY HIERARCHIES AND THE DISTRIBUTION OF CITY SIZE: A RECONSIDERATION OF BECKMANN'S CONTRIBUTION.
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- Journal of Regional Science, 1969, v. 9, n. 2, p. 239, doi. 10.1111/j.1467-9787.1969.tb01337.x
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Design, synthesis, brine shrimp lethality and cytotoxicity of some novel 17a-aza-D-homo-androster-17-one derivatives.
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- Natural Product Research, 2021, v. 35, n. 21, p. 3985, doi. 10.1080/14786419.2020.1753049
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Synthesis of nitrogen-containing monoterpenoids with antibacterial activity.
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- Natural Product Research, 2020, v. 34, n. 8, p. 1074, doi. 10.1080/14786419.2018.1548456
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Novel Brønsted Acidic Ionic Liquids as High Efficiency Catalysts for Liquid-Phase Beckmann Rearrangement.
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- Catalysts (2073-4344), 2023, v. 13, n. 6, p. 978, doi. 10.3390/catal13060978
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Green and efficient Beckmann rearrangement by Cu(II) contained nano‐silica triazine based dendrimer in water.
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- Journal of the Chinese Chemical Society, 2021, v. 68, n. 5, p. 893, doi. 10.1002/jccs.202000469
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Alkaline Synthesis of Pure Silica ITH Zeolite for Vapor Phase Beckmann Rearrangement of Cyclohexanone Oxime.
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- Chemistry - An Asian Journal, 2025, v. 20, n. 1, p. 1, doi. 10.1002/asia.202401057
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Corrigendum to: Synthesis of Tetracyclic Fused Quinolines via a Friedel–Crafts and Beckmann Ring Expansion Sequence.
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- Australian Journal of Chemistry, 2019, v. 72, n. 12, p. 990, doi. 10.1071/CH19363_CO
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Synthesis of Tetracyclic Fused Quinolines via a Friedel–Crafts and Beckmann Ring Expansion Sequence.
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- Australian Journal of Chemistry, 2019, v. 72, n. 12, p. 945, doi. 10.1071/CH19363
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Diversity-oriented synthesis of benzo[b]thiophenes fused to medium-sized N-heterocycles via Friedel--Crafts cyclization processes.
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- ARKIVOC: Online Journal of Organic Chemistry, 2023, v. 2023, p. 1, doi. 10.24820/ark.5550190.p011.986
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Steroidal lactams: a review.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 262, doi. 10.24820/ark.5550190.p011.773
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Beckmann rearrangement for the synthesis of derivatives of β- and γ-carbolinones, dihydropyrrolopyridinone and tetrahydroisoquinolinone.
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- ARKIVOC: Online Journal of Organic Chemistry, 2015, v. 2015, p. 362, doi. 10.3998/ark.5550190.p009.291
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Deactivation kinetic study on vapor phase Beckmann rearrangement of cyclohexanone oxime and design of the multi-layer inclined channel bionic reactor.
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- Chemical Engineering Research & Design: Transactions of the Institution of Chemical Engineers Part A, 2023, v. 190, p. 476, doi. 10.1016/j.cherd.2022.12.031
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Synthesis of some (E)-3-arylidene-7-methylazepan-2-ones via Beckmann rearrangement.
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- Chemistry & Biology Interface, 2016, v. 6, n. 5, p. 312
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Synthesis of some (E)-3-arylidene-6-methylpiperidin-2-ones via Beckmann rearrangement.
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- Chemistry & Biology Interface, 2016, v. 6, n. 4, p. 198
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Creating Accessible Active Sites in Hierarchical MFI Zeolites for Low-Temperature Acid Catalysis.
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- ChemCatChem, 2016, v. 8, n. 19, p. 3161, doi. 10.1002/cctc.201600729
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Extra-Large-Pore Zeolites with UTL Topology: Control of the Catalytic Activity by Variation in the Nature of the Active Sites.
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- ChemCatChem, 2013, v. 5, n. 7, p. 1891, doi. 10.1002/cctc.201200925
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Falsely elevated troponin I results due to outliers indicate a lack of analytical robustness.
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- Annals of Clinical Biochemistry, 2010, v. 47, n. 3, p. 242, doi. 10.1258/acb.2010.010012
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Beckmann rearrangement of cyclohexanone oxime in a microchemical system: The role of SO<sub>3</sub> and product inhibition.
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- AIChE Journal, 2012, v. 58, n. 10, p. 3156, doi. 10.1002/aic.13715
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Beckmann Rearrangement of Cyclohexanone Oxime to ε -Caprolactam in Microreactors.
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- AIChE Journal, 2010, v. 56, n. 5, p. 1297, doi. 10.1002/aic.12051
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Beckmann Rearrangement of Cyclohexanone Oxime in a Microreactor Setup with Internal Recirculation.
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- Chemical Engineering & Technology, 2013, v. 36, n. 8, p. 1387, doi. 10.1002/ceat.201300088
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Green synthesis of reduced graphene oxide anchored Fe<sub>3</sub>O<sub>4</sub>‐Pd hetero‐nanostructure: An efficient, magnetically separable and reusable catalyst for Beckmann rearrangement of aldoximes to amides.
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- Applied Organometallic Chemistry, 2023, v. 37, n. 12, p. 1, doi. 10.1002/aoc.7275
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A Short and Versatile Approach for the Synthesis of Pyrrolizidinones.
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- Helvetica Chimica Acta, 2022, v. 105, n. 3, p. 1, doi. 10.1002/hlca.202100226
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Design, Synthesis, and Bioassay of Novel Compounds of Isolongifolenone Oxime Derivatives.
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- Helvetica Chimica Acta, 2016, v. 99, n. 9, p. 696, doi. 10.1002/hlca.201600133
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Citric acid catalysed Beckmann rearrangement, under solvent free conditions.
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- Journal of Chemical Research, 2011, v. 35, n. 2, p. 124, doi. 10.3184/174751911X557296
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A Beckmann rearrangement initiated by trifluoromethanesulfonic anhydride in the synthesis of compounds containing a new pyrazolo[3',4':5,6]pyrido[3,2-b]azepine heterocyclic system.
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- Chemistry of Heterocyclic Compounds, 2021, v. 57, n. 2, p. 199, doi. 10.1007/s10593-021-02893-8
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Hydrogenated benzazepines: recent advances in the synthesis and study of biological activity.
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- Chemistry of Heterocyclic Compounds, 2019, v. 55, n. 9, p. 802, doi. 10.1007/s10593-019-02540-3
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Substituted quinolinones 27.* Regioselective synthesis of pyrazolo-, oxazolo-, and triazepinoquinoline derivatives.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 11/12, p. 1023, doi. 10.1007/s10593-016-1813-y
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Symmetrical and Unsymmetrical Bis-1,1′-(3,4-dihydroisoquinolines).
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- Chemistry of Heterocyclic Compounds, 2005, v. 41, n. 4, p. 475, doi. 10.1007/s10593-005-0174-8
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Anomalous Beckmann Reaction of 4-Aryl-2,7,7-trimethyl-5-oxo-5,6,7,8-tetrahydroquinoline Oximes in Polyphosphoric Acid. 1. New Synthesis of 1-Ethoxycarbonyl-2,5,5-trimethyl-5,6-dihydro-4H-pyrido[2,3,4-k,l]acridines.
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- Chemistry of Heterocyclic Compounds, 2003, v. 39, n. 12, p. 1627
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An Expeditious Approach to the Synthesis of Novel Quinolino and Diazacino Condensed Analogues of Azepino [3, 2-b] Carbazole-2-one of Medicinal Interest.
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- Indian Journal of Pharmaceutical Education & Research, 2022, v. 56, p. 89, doi. 10.5530/ijper.56.1s.47
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Investigation of O‐Sulfonylation‐promoted Heterolytic NO Bond Cleavage of Amidoximes and Ketoximes.
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- Journal of the Chinese Chemical Society, 2018, v. 65, n. 3, p. 325, doi. 10.1002/jccs.201700104
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Application of Mixed Acid-Modified Hollow TS-1 Zeolite to Vapor-Phase Beckman Rearrangement Reaction.
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- Catalysis Letters, 2024, v. 154, n. 11, p. 6035, doi. 10.1007/s10562-024-04780-1
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A New Sustainable Multistep Catalytic Process from Benzene to Caprolactam: Amination, Hydroximation and Beckmann Rearrangement Promoted and Catalyzed by Trifluoroacetic Acid.
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- Catalysis Letters, 2023, v. 153, n. 9, p. 2763, doi. 10.1007/s10562-022-04207-9
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Trifluoroacetic Acid Hydroxylamine System as Organocatalyst Reagent in a One-Pot Salt Free Process for the Synthesis of Caprolactam and Amides of Industrial Interest.
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- Catalysis Letters, 2021, v. 151, n. 12, p. 3543, doi. 10.1007/s10562-021-03590-z
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Controllable Synthesis and Structure-Performance Relationship of Silicalite-1 Nanosheets in Vapor Phase Beckmann Rearrangement of Cyclohexanone Oxime.
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- Catalysis Letters, 2021, v. 151, n. 5, p. 1488, doi. 10.1007/s10562-020-03404-8
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Beckmann Rearrangement of Cyclohexanone Oxime to ε-Caprolactam in a Modified Catalytic System of Trifluoroacetic Acid.
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- Catalysis Letters, 2014, v. 144, n. 1, p. 151, doi. 10.1007/s10562-013-1114-3
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Selectively Obtaining ε-Caprolactam from Cyclohexanone Oxime Over Al-MCM-41 Catalysts.
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- Catalysis Letters, 2013, v. 143, n. 4, p. 333, doi. 10.1007/s10562-013-0971-0
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Heterogeneous Beckmann Rearrangements Catalyzed by a Sulfonated Imidazolium Salt of Phosphotungstate.
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- Catalysis Letters, 2013, v. 143, n. 2, p. 193, doi. 10.1007/s10562-012-0939-5
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Cu/SBA-15 is an Efficient Solvent-Free and Acid-Free Catalyst for the Rearrangement of Benzaldoxime into Benzamide.
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- Catalysis Letters, 2011, v. 141, n. 12, p. 1865, doi. 10.1007/s10562-011-0713-0
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