Works matching DE "CLAISEN rearrangement"
Results: 240
Synthesis of (±)-Sundiversifolide Based on Lewis Acid-Mediated Claisen Rearrangement.
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- Bioscience, Biotechnology & Biochemistry, 2007, v. 71, n. 8, p. 2046, doi. 10.1271/bbb.70283
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Preparation of Renewable Thiol‐Yne "Click" Networks Based on Fractionated Lignin for Anticorrosive Protective Film Applications.
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- Macromolecular Chemistry & Physics, 2022, v. 223, n. 13, p. 1, doi. 10.1002/macp.202100461
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Aliphatic Ketone Claisen Rearrangement: Troubleshooting the Transetherification Step by Identifying a Stable Acid Catalyst.
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- Chemistry - A European Journal, 2024, v. 30, n. 53, p. 1, doi. 10.1002/chem.202402371
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Exploring a De Novo Route to Bradyrhizose: Synthesis and Isomeric Equilibrium of Bradyrhizose Diastereomers<sup>≠</sup>.
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- Chemistry - A European Journal, 2024, v. 30, n. 33, p. 1, doi. 10.1002/chem.202400886
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Toward Efficient and Stereoselective Aromatic and Dearomative Cope Rearrangements: Experimental and Theoretical Investigations of α‐Allyl‐α'‐Aromatic γ‐Lactone Derivatives.
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- Chemistry - A European Journal, 2024, v. 30, n. 21, p. 1, doi. 10.1002/chem.202304138
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Recent Developments on Photochemical Synthesis of 1,n‐Dicarbonyls.
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- Chemistry - A European Journal, 2023, v. 29, n. 49, p. 1, doi. 10.1002/chem.202301147
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Synthesis of 2,2‐Disubstituted 2H‐Chromenes through Carbon‐Carbon Bond Formation Utilizing a [1,2]‐Phospha‐Brook Rearrangement under Brønsted Base Catalysis.
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- Chemistry - A European Journal, 2022, v. 28, n. 45, p. 1, doi. 10.1002/chem.202201198
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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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Stereoselective Synthesis of Polysubstituted Conjugated Dienes Enabled by Photo‐Driven Sequential Sigmatropic Rearrangement.
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- Angewandte Chemie, 2024, v. 136, n. 24, p. 1, doi. 10.1002/ange.202400805
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Novel Stereo‐Induction Pattern in Pudovik Addition/Phospha‐Brook Rearrangement Towards Chiral Trisubstituted Allenes.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202403707
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Multicomponent Cyclizative 1,2‐Rearrangement Enabled Enantioselective Construction of 2,2‐Disubstituted Pyrrolinones.
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- Angewandte Chemie, 2024, v. 136, n. 7, p. 1, doi. 10.1002/ange.202317182
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Copper‐Catalyzed Oxygenative Skeletal Rearrangement of Tetrahydro‐β‐carbolines Using H<sub>2</sub>O and O<sub>2</sub> as Oxygen Sources.
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- Angewandte Chemie, 2023, v. 135, n. 51, p. 1, doi. 10.1002/ange.202313687
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Defluorinative Multi‐Functionalization of Fluoroaryl Sulfoxides Enabled by Fluorine‐Assisted Temporary Dearomatization.
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- Angewandte Chemie, 2023, v. 135, n. 36, p. 1, doi. 10.1002/ange.202306914
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Cobalt‐Catalyzed Wagner–Meerwein Rearrangements with Concomitant Nucleophilic Hydrofluorination.
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- Angewandte Chemie, 2023, v. 135, n. 35, p. 1, doi. 10.1002/ange.202308048
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σ‐Cyclopropyl to π‐Allyl Rearrangement at Au<sup>III</sup>.
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- Angewandte Chemie, 2023, v. 135, n. 31, p. 1, doi. 10.1002/ange.202305280
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Total Synthesis of Lucidumone through Convenient One‐pot Preparation of the Tetracyclic Skeleton by Claisen Rearrangement and Subsequent Intramolecular Aldol Reaction.
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- Angewandte Chemie, 2023, v. 135, n. 24, p. 1, doi. 10.1002/ange.202304132
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N‐(Morpholine‐4‐dithio)phthalimide: A Shelf‐Stable, Bilateral Platform Molecule Enabling Access to Diverse Unsymmetrical Disulfides**.
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- Angewandte Chemie, 2023, v. 135, n. 18, p. 1, doi. 10.1002/ange.202219156
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Iridium‐Catalyzed Chemo‐, Diastereo‐, and Enantioselective Allyl‐Allyl Coupling: Accessing All Four Stereoisomers of (E)‐1‐Boryl‐Substituted 1,5‐Dienes by Chirality Pairing.
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- Angewandte Chemie, 2023, v. 135, n. 13, p. 1, doi. 10.1002/ange.202218794
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I<sub>2</sub>‐Catalyzed Cycloisomerization of Ynamides: Chemoselective and Divergent Access to Indole Derivatives.
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- Angewandte Chemie, 2023, v. 135, n. 8, p. 1, doi. 10.1002/ange.202215616
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Synthesis of Chiral Endocyclic Allenes by Palladium‐Catalyzed Asymmetric Annulation Followed by Cope Rearrangement.
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- Angewandte Chemie, 2022, v. 134, n. 24, p. 1, doi. 10.1002/ange.202117215
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Brønsted Acid Catalyzed Dearomatization by Intramolecular Hydroalkoxylation/Claisen Rearrangement: Diastereo‐ and Enantioselective Synthesis of Spirolactams.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27370, doi. 10.1002/ange.202113464
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Photoredox Catalytic Phosphite‐Mediated Deoxygenation of α‐Diketones Enables Wolff Rearrangement and Staudinger Synthesis of β‐Lactams.
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- Angewandte Chemie, 2021, v. 133, n. 36, p. 19848, doi. 10.1002/ange.202107080
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Alkene Isomerization Revitalizes the Coates–Claisen Rearrangement.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18657, doi. 10.1002/ange.202105834
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Asymmetric Catalytic Vinylogous Addition Reactions Initiated by Meinwald Rearrangement of Vinyl Epoxides.
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- Angewandte Chemie, 2021, v. 133, n. 26, p. 14642, doi. 10.1002/ange.202102054
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Concise Biosynthesis of Phenylfuropyridones in Fungi.
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- Angewandte Chemie, 2020, v. 132, n. 45, p. 20061, doi. 10.1002/ange.202008321
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A 1,3,2‐Diazaphospholene‐Catalyzed Reductive Claisen Rearrangement.
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- Angewandte Chemie, 2019, v. 131, n. 26, p. 8985, doi. 10.1002/ange.201904411
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Bimetallic Rhodium(II)/Indium(III) Relay Catalysis for Tandem Insertion/Asymmetric Claisen Rearrangement.
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- Angewandte Chemie, 2018, v. 130, n. 50, p. 16792, doi. 10.1002/ange.201810410
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Conversion of an Arabinose-Derived Allyl Vinyl Ether System into the Functionalized 4-Cycloheptenone via Claisen Rearrangement.
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- Journal of Carbohydrate Chemistry, 2005, v. 24, n. 8/9, p. 843, doi. 10.1080/07328300500434224
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Synthesis and biological evaluation of fused oxepinocoumarins as free radicals scavengers.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2011, v. 26, n. 6, p. 805, doi. 10.3109/14756366.2011.555944
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Assessing the accuracy and efficacy of multiscale computational methods in predicting reaction mechanisms and kinetics of S<sub>N</sub>2 reactions and Claisen rearrangement.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-67468-x
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Exploring the Mechanism of Catalysis with the Unified Reaction Valley Approach (URVA)—A Review.
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- Catalysts (2073-4344), 2020, v. 10, n. 6, p. 691, doi. 10.3390/catal10060691
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A short formal total synthesis of (±)-hirsutic acid.
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- Canadian Journal of Chemistry, 2012, v. 90, n. 11, p. 927, doi. 10.1139/v2012-037
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A short formal total synthesis of (±)-hirsutic acid.
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- Canadian Journal of Chemistry, 2012, v. 90, n. 11, p. 927, doi. 10.1139/v2012-037
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Regioselective synthesis of biologically interesting pentacyclic polyheterocycles by sequential thio-Claisen and AlCl<sub>3</sub> catalyzed oxy-Claisen rearrangement of 4-(4′-aryloxybut-2′-ynylthio)-1-phenyl-1,8-naphthyridin-2(1H)-one.
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- Canadian Journal of Chemistry, 2006, v. 84, n. 12, p. 1632, doi. 10.1139/V06-174
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SnCl<sub>4</sub>–I<sub>2</sub> mediated regioselective 6-endo- and 5-exo-cyclization of ortho-allylenols.
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- Canadian Journal of Chemistry, 2005, v. 83, n. 12, p. 2046, doi. 10.1139/V05-212
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Degradation of the strobilurin fungicide mandestrobin in illuminated water--sediment systems.
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- Journal of Pesticide Science, 2024, v. 49, n. 1, p. 38, doi. 10.1584/jpestics.D23-056
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Regioselective synthesis of pentacyclic heterocycles by the thermal and Lewis acid catalyzed Claisen rearrangement.
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- Journal of Sulfur Chemistry, 2009, v. 30, n. 5, p. 481, doi. 10.1080/17415990902725709
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Claisen-Schmidt condensation: Synthesis of (1S,6R)/(1R,6S)-2-oxo-N,4,6-triarylcyclohex-3-enecarboxamide derivatives with different substituents in H<sub>2</sub>O/EtOH.
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- Chirality, 2016, v. 28, n. 11, p. 728, doi. 10.1002/chir.22653
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A new reaction mechanism of Claisen rearrangement induced by few-optical-cycle pulses: Demonstration of nonthermal chemistry by femtosecond vibrational spectroscopy.
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- Pure & Applied Chemistry, 2013, v. 85, n. 10, p. 1991, doi. 10.1351/PAC-CON-12-12-01
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An acyl-Claisen approach to the synthesis of lignans and substituted pyrroles.
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- Pure & Applied Chemistry, 2012, v. 84, n. 7, p. 1557, doi. 10.1351/PAC-CON-11-09-27
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Aromaticity of Cope and Claisen rearrangements.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2023, v. 142, n. 5, p. 1, doi. 10.1007/s00214-023-02975-0
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A spin-coupled study of the Claisen rearrangement of allyl vinyl ether.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2006, v. 115, n. 4, p. 212, doi. 10.1007/s00214-005-0007-y
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Exploring the quantum mechanical/molecular mechanical replica path method: a pathway optimization of the chorismate to prephenate Claisen rearrangement catalyzed by chorismate mutase.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2003, v. 109, n. 3, p. 140, doi. 10.1007/s00214-002-0421-3
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加成型酚醛改性双马树脂及其复合材料性能.
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- Acta Materiae Compositae Sinica, 2023, v. 40, n. 2, p. 741, doi. 10.13801/j.cnki.fhclxb.20220321.004
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Tunable Gold‐catalyzed Reactions of Propargyl Alcohols and Aryl Nucleophiles.
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- ChemistryOpen, 2022, v. 11, n. 5, p. 1, doi. 10.1002/open.202200030
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A Dataset of Computational Reaction Barriers for the Claisen Rearrangement: Chemical and Numerical Analysis.
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- Molecular Informatics, 2022, v. 41, n. 3, p. 1, doi. 10.1002/minf.202100216
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Ytterbium‐Catalyzed Tandem Diels–Alder/Claisen Rearrangement/Decarboxylation of Hetero‐Allenes for the Synthesis of Diarylmethanes.
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- Chinese Journal of Chemistry, 2025, v. 43, n. 2, p. 199, doi. 10.1002/cjoc.202400874
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Synthesis of 2-Amino-2-deoxy-1,3-dithioidoglycosides via Organocatalytic Relay Glycosylation of 3-O-Acetyl-2-nitrogalactals.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 21, p. 2837, doi. 10.1002/cjoc.202300307
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Gold Self‐Relay Catalysis Enabling [3,3]‐Sigmatropic Rearrangement/Nazarov Cyclization and Allylic Alkylation Cascade for Constructing All‐Carbon Quaternary Stereocenters.
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- Chinese Journal of Chemistry, 2022, v. 40, n. 6, p. 687, doi. 10.1002/cjoc.202100734
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Synthesis of some novel pyrano[2,3- f]chromenone derivatives.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 4, p. 605, doi. 10.1007/s13738-014-0518-3
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