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Reaction of singlet-excited 2,3-diazabicyclo[2.2.2]oct-2-ene and tert-butoxyl radicals with aryl-substituted benzofuranones

Author
LUNDGREN, Cecilia Vannesjo1 ; KONER, Apurba L1 ; TINKI, Michael2 ; PISCHEL, Uwe3 ; NAU, Werner M1
[1] School of Engineering and Science, International University Bremen, Campus Ring 1, 28759 Bremen, Germany
[2] Ciba Specialty Chemicals, Plastic Additives, R-1059.4.02, 4002 Basel, Switzerland
[3] REQUIMTE/Departamento de Química, Universidade do Porto, Rua Campo Alegre, 4169-007 Porto, Portugal
Source

Journal of organic chemistry. 2006, Vol 71, Num 5, pp 1977-1983, 7 p ; ref : 70 ref

CODEN
JOCEAH
ISSN
0022-3263
Scientific domain
Biochemistry, molecular biology, biophysics; Organic chemistry
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Alcoxyle Antioxydant Composé aromatique Composé benzylique Composé éthylénique Donneur électron Electrophile Energie libre Enlèvement hydrogène Etat singulet Fluorescence Hétérocycle oxygène Lactone Nucléophile Optimisation Radical libre organique Vitesse réaction Benzofuran-2-one dérivé
Keyword (en)
Alkoxyl Antioxidant Aromatic compound Benzylic compound Ethylenic compound Electron donor Electrophile Free energy Hydrogen abstraction Singlet state Fluorescence Oxygen heterocycle Lactone Nucleophile Optimization Organic free radical Reaction rate
Keyword (es)
Alcoxilo Antioxidante Compuesto aromático Compuesto benzílico Compuesto etilénico Donador electrón Electrófilo Energía libre Abstracción hidrógeno Estado singular Fluorescencia Heterociclo oxígeno Lactona Nucleófilo Optimización Radical libre orgánico Velocidad reacción
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
17741397

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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