Works matching DE "PERICYCLIC reactions"
Results: 130
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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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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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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Rehybridization dynamics into the pericyclic minimum of an electrocyclic reaction imaged in real-time.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38513-6
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Interrogating chemical mechanisms in natural products biosynthesis using quantum chemical calculations.
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- WIREs: Computational Molecular Science, 2020, v. 10, n. 3, p. 1, doi. 10.1002/wcms.1453
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PhI(OAc)<sub>2</sub>‐Promoted 1,2‐Diaza‐Cope Rearrangement of β,γ‐Unsaturated Hydrazones with Acetate/H<sub>2</sub>O: Access to Diacyl/Acyl N‐Allylhydrazines.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 33, p. 5464, doi. 10.1002/ejoc.202000875
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Generating Skeletal Diversity and Complexity from Boron‐Substituted 1,3‐Dienes and Enophiles.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 22, p. 3282, doi. 10.1002/ejoc.202000330
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Biosynthetic Interrelationships within Polycyclic Cembranoids Isolated from Corals: Conjecture, Biomimetic Synthesis and Reality.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 16, p. 2330, doi. 10.1002/ejoc.201901438
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Study of the Oxidative Cleavage Proposed in the Biogenesis of Transtaganolides/Basiliolides: Pyran‐2‐one Aromaticity‐Mediated Regioselective Control and Biogenetic Implications.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 11, p. 1673, doi. 10.1002/ejoc.201901894
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4‐π‐Photocyclization: Scope and Synthetic Applications.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 10, p. 1405, doi. 10.1002/ejoc.201901230
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Synthesis of Diazanorcaradienes and 1,2‐Diazepines via the Tandem [4+2]‐Cycloaddition/Retro‐[4+2]‐Cycloaddition Reaction between Methoxycarbonylcyclopropenes and Dimethoxycarbonyltetrazine.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 26, p. 4133, doi. 10.1002/ejoc.201801861
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Concerted Albeit Not Pericyclic Cycloadditions: Understanding the Mechanism of the (4+3) Cycloaddition between Nitrones and 1,2‐Diaza‐1,3‐dienes.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 2/3, p. 391, doi. 10.1002/ejoc.201800663
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The Mysticism of Pericyclic Reactions: A Contemporary Rationalisation of Organic Reactivity Based on Electron Density Analysis.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 9, p. 1107, doi. 10.1002/ejoc.201701350
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Ester-Substituted Electron-Poor Alkenes for Cycloaddition-Retroelectrocyclization (CA-RE) and Related Reactions.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 33, p. 7264, doi. 10.1002/ejoc.201501085
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An Organocatalytic Cope Rearrangement.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 38, p. 11557, doi. 10.1002/anie.201606480
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Concise Total Synthesis of Enigmazole A.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 4, p. 1406, doi. 10.1002/anie.201510026
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Density functional insights on the role of iron tricarbonyl in manipulating the ring opening of 4π-hetero cyclobutane analogues – a shift from pseudopericyclic to pericyclic.
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- Journal of Chemical Sciences, 2024, v. 136, n. 3, p. 1, doi. 10.1007/s12039-024-02278-2
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[1, 5]-halo shift in perturbed pericyclic system of heterosubstituted pentadienes - a DFT exploration.
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- Journal of Chemical Sciences, 2022, v. 134, n. 4, p. 1, doi. 10.1007/s12039-022-02096-4
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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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Anomalous Direction of the Ene Reaction of Pulegone with 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 9, p. 1430, doi. 10.1134/S1070428018090294
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Ene Reaction of β-Pinene with 4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione: Effects of Temperature, High Pressure, and Solvent Nature.
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- Russian Journal of Organic Chemistry, 2018, v. 54, n. 7, p. 1080, doi. 10.1134/S1070428018070187
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A DFT Study of Inter- and Intramolecular Aryne Ene Reactions.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 13, p. 2826, doi. 10.1002/ejoc.201500139
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Pericyclic Reactions of Azafulvenium Methides Bearing Internal Dipolarophiles - Synthesis of Chromene and Chromane Derivatives.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 6, p. 1341, doi. 10.1002/ejoc.201403407
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A Divergent Enantioselective Synthesis of 9-J<sub>1</sub>-Phytoprostane and 9-A<sub>1</sub>-Phytoprostane Methyl Ester.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 10, p. 2111, doi. 10.1002/ejoc.201301703
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Syntheses of New Carbanucleosides by Pericyclic Reactions.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 18, p. 3835, doi. 10.1002/ejoc.201300202
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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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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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Regulatory networks controlling the development of the root system and the formation of lateral roots: a comparative analysis of the roles of pericycle and vascular cambium.
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- Annals of Botany, 2018, v. 122, n. 5, p. 697, doi. 10.1093/aob/mcy003
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Self-propelled assembly of nanoparticles with self-catalytic regulation for tumour-specific imaging and therapy.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-44736-y
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- Article
Flash Vacuum Pyrolysis: Principles, Instrumentation, and Applications.
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- Resonance: Journal of Science Education, 2024, v. 29, n. 7, p. 907, doi. 10.1007/s12045-024-0907-6
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A tale of two topologies: Woodward-hoffmann rules at your fingertips!
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- Resonance: Journal of Science Education, 2011, v. 16, n. 12, p. 1211, doi. 10.1007/s12045-011-0136-7
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- Article
Theoretical study on the mechanism of the cycloaddition reaction between ketenimine and hydrogen cyanide.
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- Journal of the Serbian Chemical Society, 2016, v. 81, n. 2, p. 187, doi. 10.2298/JSC150504091H
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Optimal control of the initiation of a pericyclic reaction in the electronic ground state.
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- Journal of Chemical Sciences, 2012, v. 124, n. 1, p. 121, doi. 10.1007/s12039-011-0199-8
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- Article
Fluorine effect on pericyclic and pseudopericyclic processes: Evidences and ab initio theory.
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- Journal of Chemical Sciences, 2009, v. 121, n. 5, p. 859, doi. 10.1007/s12039-009-0101-0
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- Article
Facile Alder-Ene Reactions of Silylallenes Involving an Allenic C(sp<sup>2</sup>)H Bond.
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- Chemistry - A European Journal, 2015, v. 21, n. 48, p. 17210, doi. 10.1002/chem.201503243
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New Horizons in Chemical Functionalization of Endohedral Metallofullerenes.
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- Molecules, 2020, v. 25, n. 16, p. 3626, doi. 10.3390/molecules25163626
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Understanding the Molecular Mechanism of the Rearrangement of Internal Nitronic Ester into Nitronorbornene in Light of the MEDT Study.
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- Molecules, 2019, v. 24, n. 3, p. 462, doi. 10.3390/molecules24030462
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β-Formyl- and β-Vinylporphyrins: Magic Building Blocks for Novel Porphyrin Derivatives.
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- Molecules, 2017, v. 22, n. 8, p. 1269, doi. 10.3390/molecules22081269
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Enantioselective Cycloaddition Reactions Catalyzed by BINOL-Derived Phosphoric Acids and N-Triflyl Phosphoramides: Recent Advances.
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- Molecules, 2015, v. 20, n. 9, p. 16103, doi. 10.3390/molecules200916103
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Bifunctionalized Allenes. Part XIII. A Convenient and Efficient Method for Regioselective Synthesis of Phosphorylated α-Hydroxyallenes with Protected and Unprotected Hydroxy Group.
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- Molecules, 2014, v. 19, n. 5, p. 6309, doi. 10.3390/molecules19056309
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Ring Expansion of Vinylaziridines through the Strain-Release Pericyclic Reaction: Recent Developments and Applications.
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- Molecules, 2013, v. 18, n. 8, p. 9650, doi. 10.3390/molecules18089650
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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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Advances in the application of named reactions in polymer synthesis.
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- High Performance Polymers, 2023, v. 35, n. 5, p. 439, doi. 10.1177/09540083221143691
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- Article
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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- Article
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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