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How Did Hypervalent Iodide Oxidant Species Influence Reaction Yield of Organoselenium-Catalzyed Oxidative Ring-Closing Reaction of (E)-4-Phenylbut-3-Enoic Acid? A Theoretical Study

https://doi.org/10.2139/ssrn.4968864
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inferredcites →https://doi.org/10.1002/1521-3773(20010803)40:15<2812::aid-anie2812>3.0.co;2-xopenalex-snapshot
IBX—New Reactions with an Old Reagent
inferredcites →https://doi.org/10.1002/anie.201610657openalex-snapshot
Organoselenium‐Catalyzed Regioselective C−H Pyridination of 1,3‐Dienes and Alkenes
inferredcites →https://doi.org/10.1002/anie.201701486openalex-snapshot
Analyzing Reaction Rates with the Distortion/Interaction‐Activation Strain Model
inferredcites →https://doi.org/10.1002/jcc.22885openalex-snapshot
Multiwfn: A multifunctional wavefunction analyzer
inferredcites →https://doi.org/10.1002/qua.560290320openalex-snapshot
Bond orders and valences from ab initio wave functions
inferredcites →https://doi.org/10.1016/j.mcat.2024.114442openalex-snapshot
Both N-F oxidant and NaF determined reaction yield in the organoselenium-catalyzed oxidative ring-closing reaction of unsaturated alcohol: A theoretical study
inferredcites →https://doi.org/10.1016/j.tet.2019.05.054openalex-snapshot
Organoselenium-catalyzed enantioselective syn-dichlorination of unbiased alkenes
inferredcites →https://doi.org/10.1016/s0957-4166(98)00031-7openalex-snapshot
Catalytic asymmetric oxyselenenylation–elimination reactions using chiral selenium compounds
inferredcites →https://doi.org/10.1021/acs.chemrev.5b00547openalex-snapshot
Advances in Synthetic Applications of Hypervalent Iodine Compounds
inferredcites →https://doi.org/10.1021/acs.chemrev.9b00338openalex-snapshot
Chiral Hypervalent Iodines: Active Players in Asymmetric Synthesis
inferredcites →https://doi.org/10.1021/acs.jctc.5b01144openalex-snapshot
Benchmarking Density Functionals on Structural Parameters of Small-/Medium-Sized Organic Molecules
inferredcites →https://doi.org/10.1021/acs.joc.2c01765openalex-snapshot
Mechanistic Insight into Phenol Dearomatization by Hypervalent Iodine: Direct Detection of a Phenoxenium Cation
inferredcites →https://doi.org/10.1021/acs.joc.8b03179openalex-snapshot
Selenium-Catalyzed Oxidative C–H Amination of (E)-3-(Arylamino)-2-styrylquinazolin-4(3H)-ones: A Metal-Free Synthesis of 1,2-Diarylpyrazolo[5,1-b]quinazolin-9(1H)-ones
inferredcites →https://doi.org/10.1021/acs.joc.9b02784openalex-snapshot
Stepwise Mechanism for the Bromination of Arenes by a Hypervalent Iodine Reagent
inferredcites →https://doi.org/10.1021/acs.orglett.0c01288openalex-snapshot
Organoseleno-Catalyzed Synthesis of α,β-Unsaturated α′-Alkoxy Ketones from Allenes Enabled by Se···O Interactions
inferredcites →https://doi.org/10.1021/acs.orglett.5b00213openalex-snapshot
Organoselenium-Catalyzed, Hydroxy-Controlled Regio- and Stereoselective Amination of Terminal Alkenes: Efficient Synthesis of 3-Amino Allylic Alcohols
inferredcites →https://doi.org/10.1021/acs.orglett.5b01156openalex-snapshot
Selenium-Catalyzed Oxidative C(sp2)–H Amination of Alkenes Exemplified in the Expedient Synthesis of (Aza-)Indoles
inferredcites →https://doi.org/10.1021/acs.orglett.5b03543openalex-snapshot
Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles
inferredcites →https://doi.org/10.1021/acscatal.3c03524openalex-snapshot
Electrophilic Selenium-Catalyzed Desymmetrizing Cyclization to Access P-Stereogenic Heterocycles
inferredcites →https://doi.org/10.1021/acscatal.7b00975openalex-snapshot
Hypercoordinate Iodine Catalysts in Enantioselective Transformation: The Role of Catalyst Folding in Stereoselectivity
inferredcites →https://doi.org/10.1021/acscatal.7b01216openalex-snapshot
Oxidative Alkene Functionalizations via Selenium-π-Acid Catalysis
inferredcites →https://doi.org/10.1021/acscatal.7b03829openalex-snapshot
Organoselenium-Catalyzed Oxidative Allylic Fluorination with Electrophilic N–F Reagent
inferredcites →https://doi.org/10.1021/ar00072a001openalex-snapshot
The path of chemical reactions - the IRC approach
inferredcites →https://doi.org/10.1021/ar00109a003openalex-snapshot
Atoms in molecules
inferredcites →https://doi.org/10.1021/cr00005a013openalex-snapshot
A quantum theory of molecular structure and its applications
inferredcites →https://doi.org/10.1021/ct100641aopenalex-snapshot
NCIPLOT: A Program for Plotting Noncovalent Interaction Regions
inferredcites →https://doi.org/10.1021/ed058p32openalex-snapshot
What is the rate-limiting step of a multistep reaction?
inferredcites →https://doi.org/10.1021/ja00019a027openalex-snapshot
A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species
inferredcites →https://doi.org/10.1021/ja0734086openalex-snapshot
Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity
inferredcites →https://doi.org/10.1021/ja100936wopenalex-snapshot
Revealing Noncovalent Interactions
inferredcites →https://doi.org/10.1021/ja800009zopenalex-snapshot
Theory of 1,3-Dipolar Cycloadditions: Distortion/Interaction and Frontier Molecular Orbital Models
inferredcites →https://doi.org/10.1021/jacs.1c06750openalex-snapshot
Catalytic, Enantioselective Syn -Oxyamination of Alkenes
inferredcites →https://doi.org/10.1021/jacs.6b01462openalex-snapshot
A Chiral Electrophilic Selenium Catalyst for Highly Enantioselective Oxidative Cyclization
inferredcites →https://doi.org/10.1021/jacs.6b07999openalex-snapshot
Acid Activation in Phenyliodine Dicarboxylates: Direct Observation, Structures, and Implications
inferredcites →https://doi.org/10.1021/jacs.9b11261openalex-snapshot
Catalytic, Enantioselective syn- Diamination of Alkenes
inferredcites →https://doi.org/10.1021/jo9824596openalex-snapshot
A User-Friendly Entry to 2-Iodoxybenzoic Acid (IBX)
inferredcites →https://doi.org/10.1021/jp810292nopenalex-snapshot
Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions
inferredcites →https://doi.org/10.1021/ol071223yopenalex-snapshot
Catalytic Use of Selenium Electrophiles in Cyclizations
inferredcites →https://doi.org/10.1021/ol202800kopenalex-snapshot
Selenium-Catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants
inferredcites →https://doi.org/10.1021/ol503161gopenalex-snapshot
Mechanistic Insights on Iodine(III) Promoted Metal-Free Dual C–H Activation Involved in the Formation of a Spirocyclic Bis-oxindole
inferredcites →https://doi.org/10.1038/nchem.2141openalex-snapshot
Catalytic, stereospecific syn-dichlorination of alkenes
inferredcites →https://doi.org/10.1039/b508541aopenalex-snapshot
Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy
inferredcites →https://doi.org/10.1039/c5qo00179jopenalex-snapshot
Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination
inferredcites →https://doi.org/10.1039/c8cy02274gopenalex-snapshot
Selenium reagents as catalysts
inferredcites →https://doi.org/10.1039/c9nj00964gopenalex-snapshot
Organoselenium small molecules as catalysts for the oxidative functionalization of organic molecules
inferredcites →https://doi.org/10.1039/d0cc05354fopenalex-snapshot
Hypervalent iodine reagent-mediated reactions involving rearrangement processes
inferredcites →https://doi.org/10.1039/d0nj00837kopenalex-snapshot
Oxidative ability of organic iodine( iii ) reagents: a theoretical assessment
inferredcites →https://doi.org/10.1039/d1gc00961copenalex-snapshot
Selenium-catalyzed selective reactions of carbonyl derivatives: state-of-the-art and future challenges
inferredcites →https://doi.org/10.1039/d1ob02233dopenalex-snapshot
Updates on hypervalent-iodine reagents: metal-free functionalisation of alkenes, alkynes and heterocycles
inferredcites →https://doi.org/10.1039/d2ob00741jopenalex-snapshot
Iodine( iii ) reagents for oxidative aromatic halogenation
inferredcites →https://doi.org/10.1039/d3ob01964kopenalex-snapshot
Phenyliodine bis(trifluoroacetate) as a sustainable reagent: exploring its significance in organic synthesis
inferredcites →https://doi.org/10.1063/1.1949201openalex-snapshot
A post-Hartree–Fock model of intermolecular interactions
inferredcites →https://doi.org/10.1063/1.2065267openalex-snapshot
A density-functional model of the dispersion interaction
inferredcites →https://doi.org/10.1063/1.2190220openalex-snapshot
A post-Hartree-Fock model of intermolecular interactions: Inclusion of higher-order corrections
inferredcites →https://doi.org/10.1063/1.3382344openalex-snapshot
A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu
inferredcites →https://doi.org/10.1063/1.449486openalex-snapshot
Natural population analysis
inferredcites →https://doi.org/10.1063/1.456010openalex-snapshot
An improved algorithm for reaction path following
inferredcites →https://doi.org/10.1093/oso/9780198551683.001.0001openalex-snapshot
Atoms in Molecules
inferredcites →https://doi.org/10.1103/physrevlett.77.3865openalex-snapshot
Generalized Gradient Approximation Made Simple
inferredcites →https://doi.org/10.2174/1570179419666220211102602openalex-snapshot
Recent Advances in Organoselenium Catalysis
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