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Enantioselective α-benzylation of aldehydes via photoredox organocatalysisDirect catalytic anti-Markovnikov addition of carboxylic acids to alkenesReactivities of substituted α-phenyl-N-tert-butyl nitronesRadical-based regioselective C-H functionalization of electron-deficient heteroarenes: scope, tunability, and predictability.On the electrophilic character of molecules through its relation with electronegativity and chemical hardness.Pushing the boundaries of intrinsically stable radicals: inverse design using the thiadiazinyl radical as a template.Stress induced lipid production in Chlorella vulgaris: relationship with specific intracellular reactive species levels.Global and local reactivity indices for electrophilic/nucleophilic free radicals.Metal Bridging for Directing and Accelerating Electron Transfer as Exemplified by Harnessing the Reactivity of AIBN.Photochemical generation of 9H-fluorenyl radicals.Free-Radical Carbo-Alkenylation of Olefins: Scope, Limitations and Mechanistic Insights.An Experimental Radical Electrophilicity Index.Deaminative Strategy for the Visible-Light-Mediated Generation of Alkyl Radicals.Insight into the Mechanism of the Initial Reaction of an OH Radical with DNA/RNA Nucleobases: A Computational Investigation of Radiation Damage.Validation of DFT-based methods for predicting qualitative thermochemistry of large polyaromatics.Assessment of the extended Koopmans' theorem for the chemical reactivity: Accurate computations of chemical potentials, chemical hardnesses, and electrophilicity indices.Synthesis of functionalized 5-substituted thiazolidine-2-thiones via adscititious xanthate-promoted radical cyclization of allyl(alkyl/aryl)dithiocarbamates.Exchanging Alkyl Groups through Unstrained C-C Bond Cleavage in the Presence of a Copper Catalyst.Koopmans' analysis of chemical hardness with spectral-like resolution.Application of electron conformational-genetic algorithm approach to 1,4-dihydropyridines as calcium channel antagonists: pharmacophore identification and bioactivity prediction.Universal mathematical identities in density functional theory: results from three different spin-resolved representations.Visible-light-mediated generation of nitrile oxides for the photoredox synthesis of isoxazolines and isoxazoles.Formal Giese addition of C(sp)-H nucleophiles enabled by visible light mediated Ni catalysis of triplet enone diradicalsDurch sichtbares Licht vermittelte Deaminierung zur Erzeugung von AlkylradikalenNet reactivity index (Δω R±)Addition of Electrophilic Radicals to 2-Benzyloxyglycals: Synthesis and Functionalization of Fluorinated α-C-Glycosides and DerivativesConstruction of a Nanodiamond–Tamoxifen Complex as a Breast Cancer Drug Delivery Vehicle
P2860
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P2860
description
im Juli 2007 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в липні 2007
@uk
name
Electrophilicity and Nucleophilicity Index for Radicals
@en
Electrophilicity and Nucleophilicity Index for Radicals
@nl
type
label
Electrophilicity and Nucleophilicity Index for Radicals
@en
Electrophilicity and Nucleophilicity Index for Radicals
@nl
prefLabel
Electrophilicity and Nucleophilicity Index for Radicals
@en
Electrophilicity and Nucleophilicity Index for Radicals
@nl
P2093
P356
P1433
P1476
Electrophilicity and Nucleophilicity Index for Radicals
@en
P2093
Frank De Proft
Freija De Vleeschouwer
Paul Geerlings
P304
P356
10.1021/OL071038K
P407
P577
2007-07-01T00:00:00Z