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A theoretical study of reactivity and regioselectivity in the hydroxylation of adamantane by ferrate(VI)

Author
SHIOTA, Yoshihito1 ; KIHARA, Naoki1 ; KAMACHI, Takashi1 ; YOSHIZAWA, Kazunari1
[1] Institute for Fundamental Research of Organic Chemistry, Kyushu University, Fukuoka 812-8581, Japan
Source

Journal of organic chemistry. 2003, Vol 68, Num 10, pp 3958-3965, 8 p

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)
Adamantane Alcool Diagramme énergie Effet isotopique Etude théorique Fer VI Hydroxylation Intermédiaire réaction Longueur liaison Méthode fonctionnelle densité Radical libre organique Réactivité Régiosélectivité Structure moléculaire Ferrate
Keyword (en)
Alcohol Energy diagram Isotope effect Theoretical study Iron VI Hydroxylation Reaction intermediate Bond length Density functional method Organic free radical Reactivity Regioselectivity Molecular structure
Keyword (es)
Alcohol Diagrama energía Efecto isotópico Estudio teórico Hierro VI Hidroxilación Intermediario reacción Longitud enlace Radical libre orgánico Reactividad Regioselectividad Estructura molecular
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
14804617

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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