Works matching DE "PERICYCLIC reactions"
Results: 130
Steric Activation in the Nazarov Cyclization of Fully Substituted Divinyl Ketones.
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- Chemistry - A European Journal, 2024, v. 30, n. 72, p. 1, doi. 10.1002/chem.202402779
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Helix‐to‐Disc Conversion of Thia[6]helicenes into Coronenes Facilitated by Sulfur Oxidation and Fluorination.
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- Chemistry - A European Journal, 2024, v. 30, n. 56, p. 1, doi. 10.1002/chem.202402445
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Experimental and Theoretical Investigation of an Azaoxyallyl Cation‐Templated Intramolecular Aryl Amination Leading to Oxindole Derivatives.
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- Chemistry - A European Journal, 2022, v. 28, n. 62, p. 1, doi. 10.1002/chem.202201208
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Allyl‐Allyl Coupling Promoted by Catalyst Systems with two Palladium Atoms – A Plethora of Potentially Pericyclic Processes.
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- Angewandte Chemie, 2024, v. 136, n. 31, p. 1, doi. 10.1002/ange.202406095
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Novel Biocatalysts from Specialized Metabolism.
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- Angewandte Chemie, 2024, v. 136, n. 4, p. 1, doi. 10.1002/ange.202309284
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Durga Prasad Karothu.
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- Angewandte Chemie, 2023, v. 135, n. 34, p. 1, doi. 10.1002/ange.202306983
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Highly Stereoselective Diels–Alder Reactions Catalyzed by Diboronate Complexes.
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- Angewandte Chemie, 2023, v. 135, n. 33, p. 1, doi. 10.1002/ange.202303075
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Designing an Apparently Orbital‐Symmetry‐Forbidden [3s,5s]‐Sigmatropic Shift through Transition‐State Complexation and Stereoelectronic Effects.
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- Angewandte Chemie, 2023, v. 135, n. 17, p. 1, doi. 10.1002/ange.202300288
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Stereocontrolled Pericyclic and Radical Cycloaddition Reactions of Readily Accessible Chiral Alkenyl Diazaborolidines.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202205454
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An on‐surface Diels–Alder reaction.
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- Angewandte Chemie, 2021, v. 133, n. 50, p. 26550, doi. 10.1002/ange.202110311
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Cycloaddition Cascades of Strained Alkynes and Oxadiazinones.
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- Angewandte Chemie, 2021, v. 133, n. 33, p. 18349, doi. 10.1002/ange.202105244
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Modifying Woodward–Hoffmann Stereoselectivity Under Vibrational Strong Coupling.
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- Angewandte Chemie, 2021, v. 133, n. 11, p. 5776, doi. 10.1002/ange.202013465
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Mechanism of 3‐Methylglutaconyl CoA Decarboxylase AibA/AibB: Pericyclic Reaction versus Direct Decarboxylation.
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- Angewandte Chemie, 2020, v. 132, n. 51, p. 23173, doi. 10.1002/ange.202008919
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Heavy‐Atom Tunneling in Organic Reactions.
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 8431, doi. 10.1002/ange.201914943
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Bioinspired Synthesis of (−)‐PF‐1018.
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5301, doi. 10.1002/ange.201912452
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Cyclic Alkyne Approach to Heteroatom‐Containing Polycyclic Aromatic Hydrocarbon Scaffolds.
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- Angewandte Chemie, 2019, v. 131, n. 28, p. 9519, doi. 10.1002/ange.201903060
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A selection rule for the directions of electronic fluxes during unimolecular pericyclic reactions in the electronic ground state.
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- Molecular Physics, 2012, v. 110, n. 9/10, p. 517, doi. 10.1080/00268976.2011.648666
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Regaining the Woodward-Hoffmann rules for chelotropic reactions via conceptual DFT.
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- Canadian Journal of Chemistry, 2010, v. 88, n. 8, p. 858, doi. 10.1139/V10-049
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Activation enthalpies of pericyclic reactions: the performances of some recently proposed functionals.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2009, v. 122, n. 5/6, p. 257, doi. 10.1007/s00214-008-0503-y
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Criteria for pericyclic and pseudopericyclic character of electrocyclization of (Z)-1,2,4,6-heptatetraene and (2Z)-2,4,5-hexatriene-1-imine.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2008, v. 120, n. 1-3, p. 177, doi. 10.1007/s00214-007-0312-8
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Diels–Alder Polar Reactions of Azaheterocycles: A Theoretical and Experimental Study.
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- Organics, 2022, v. 3, n. 2, p. 102, doi. 10.3390/org3020008
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Total Synthesis of Laurane and Guaiane Sesquiterpenoids via Oxidative Nazarov Reaction.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 11, p. 1267, doi. 10.1002/cjoc.202400014
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Overview of 6π 1,5‐Electrocyclization over the Past 40 Years.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 6, p. 725, doi. 10.1002/cjoc.202200583
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A Copper‐Catalyzed [5+1] Cycloaddition of Terminal Alkynes with Diazo Esters through a Tandem 1,5‐H‐Shift Cyclization.
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- Chinese Journal of Chemistry, 2023, v. 41, n. 3, p. 301, doi. 10.1002/cjoc.202200614
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Diagnostics in computational organic chemistry.
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- Foundations of Chemistry, 2016, v. 18, n. 3, p. 241, doi. 10.1007/s10698-016-9253-4
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Pericyclases for cycloaddition.
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- National Science Review, 2022, v. 9, n. 11, p. 1, doi. 10.1093/nsr/nwac229
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Regioselectivity Switch Towards the Development of Innovative Diels‐Alder Cycloaddition and Productive Applications in Organic Synthesis.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 4, p. 1, doi. 10.1002/ajoc.202100793
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Organoboron Compounds Towards Asymmetric Pericyclic Reaction; Exploitation to Bioactive Molecule Synthesis.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 2, p. 1, doi. 10.1002/ajoc.202100092
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Natural and Synthetic Spirobutenolides and Spirobutyrolactones.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 10, p. 1377, doi. 10.1002/ajoc.202000259
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Discovery and characterization of a terpene biosynthetic pathway featuring a norbornene-forming Diels-Alderase.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30288-6
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Experiment Meets Theory: Cope Rearrangements and Thermal E/Z Isomerisations of Terpenoid Hydrocarbons.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 38, p. 1, doi. 10.1002/ejoc.202400583
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Nucleophilicities of Cyclic α‐Diazo Carbonyl Compounds.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 10, p. 1, doi. 10.1002/ejoc.202300005
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Synthesis and biological activity of potential antiviral compounds through 1,3-dipolar cycloadditions; Part 1: general aspects and reactions of azides.
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- ARKIVOC: Online Journal of Organic Chemistry, 2022, v. 2022, p. 19, doi. 10.24820/ark.5550190.p011.794
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A new life for nitrosocarbonyls in pericyclic reactions.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 418
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The role of transition-state bond-order on structure-reactivity relationships: the case of pericyclic and pseudo-pericyclic reactions.
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- ARKIVOC: Online Journal of Organic Chemistry, 2010, p. 92
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Synthesis and properties of hydrazones bearing amide, thioamide and amidine functions.
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- ARKIVOC: Online Journal of Organic Chemistry, 2010, p. 275
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Iodine‐Catalyzed Diels‐Alder Reactions.
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- ChemCatChem, 2021, v. 13, n. 12, p. 2922, doi. 10.1002/cctc.202100342
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Accuracy of auxiliary density functional theory hybrid calculations for activation and reaction enthalpies of pericyclic reactions.
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- Journal of Molecular Modeling, 2018, v. 24, n. 9, p. 1, doi. 10.1007/s00894-018-3759-8
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Woodward‐Hoffmann or Hoffmann‐Woodward? Cycloadditions and the Transformation of Roald Hoffmann from a "Calculator" to an "Explainer".
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- Chemical Record, 2024, v. 24, n. 8, p. 1, doi. 10.1002/tcr.202300181
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Introduction to "The Woodward‐Hoffmann Rules. From May 5, 1964, to November 30, 1964"**.
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- Chemical Record, 2023, v. 23, n. 2, p. 1, doi. 10.1002/tcr.202300009
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Why Woodward and Hoffmann? And Why 1965?**.
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- Chemical Record, 2023, v. 23, n. 1, p. 1, doi. 10.1002/tcr.202200239
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Why Hoffmann? His Chemistry**.
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- Chemical Record, 2022, v. 22, n. 12, p. 1, doi. 10.1002/tcr.202200205
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Why Hoffmann? The Person and the Young Chemical Physicist.
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- Chemical Record, 2022, v. 22, n. 11, p. 1, doi. 10.1002/tcr.202200196
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Catalyst-Free One-Pot Synthesis of Ketene Imines under Ultrasound Irradiation.
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- Helvetica Chimica Acta, 2014, v. 97, n. 10, p. 1422, doi. 10.1002/hlca.201400002
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Isoxazole-azirine isomerization as a reactivity switch in the synthesis of heterocycles.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 9, p. 637, doi. 10.1007/s10593-016-1944-1
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Synthesis of novel polycyclic heterosystems from 5-nitro[1,2,5]selenadiazolo[3,4- e]benzofuroxans.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 9, p. 690, doi. 10.1007/s10593-016-1950-3
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Synthesis and properties of 5-hydroxy-1-tolyl(benzyl)-1,2,3-triazoles.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 9, p. 716, doi. 10.1007/s10593-016-1953-0
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Pericyclic Reactions in the Chemistry of Heterocycles.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 9, p. 615, doi. 10.1007/s10593-016-1940-5
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Pericyclic [4+2] and [3+2] Cycloaddition Reactions of Nitroarenes in Heterocyclic Synthesis.
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- Chemistry of Heterocyclic Compounds, 2013, v. 49, n. 1, p. 92, doi. 10.1007/s10593-013-1233-1
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Remote chiral transfer into [2+2] and [2+4] cycloadditions within self-assembled molecular flasks.
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- Supramolecular Chemistry, 2011, v. 23, n. 3/4, p. 199, doi. 10.1080/10610278.2010.521833
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