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Kinetics and mechanism of the isomerization of 1H-indene-1-carboxylic acid to 1H-indene-3-carboxylic acid in aqueous solution and determination of their keto-enol equilibrium constants and acid dissociation constants of the keto and enol forms. Implications on the photolysis of diazonaphthoquinones

Author
ANDRAOS, J; KRESGE, A. J; POPIK, V. V
Univ. Toronto, dep. chemistry, Toronto ON M5S 1A1, Canada
Source

Journal of the American Chemical Society. 1994, Vol 116, Num 3, pp 961-967 ; ref : 22 ref

CODEN
JACSAT
ISSN
0002-7863
Scientific domain
Biochemistry, molecular biology, biophysics; Chemistry; Organic chemistry; Atomic molecular physics
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Acide carboxylique Composé aromatique Composé bicyclique Constante dissociation Constante vitesse Constante équilibre Equilibre chimique Etude expérimentale Isomérisation Mécanisme réaction Paramètre cinétique Propriété chimique Solution aqueuse Solution diluée Tautomérie cétoénolique Indène-1-carboxylique acide Indène-3-carboxylique acide
Keyword (en)
Carboxylic acid Aromatic compound Bicyclic compound Dissociation constant Rate constant Equilibrium constant Chemical equilibrium Experimental study Isomerization Reaction mechanism Kinetic parameter Chemical properties Aqueous solution Dilute solution Keto enol tautomerism
Keyword (es)
Acido carboxílico Compuesto aromático Compuesto bicíclico Constante disociación Constante velocidad Constante equilibrio Equilibrio químico Estudio experimental Isomerización Mecanismo reacción Parámetro cinético Propiedad química Solución acuosa Solución diluida Tautomería ceto-enólica
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B02 Kinetics and mechanisms

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4002576

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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