Direct formations of o-tropoquinone bisacetals from 2,3- and 2,7- dimethoxytropones and p-tropoquinone bisacetals from 2-bromo-7-methoxytropone by the anodic oxidation
- Auteur
- MORI, A1 ; KUBOTA, T; KASAI, S; TAKESHITA, H
[1] Kyushu univ., inst. advanced material study, Fukuoka 816, Japan - Source
Chemistry Letters. 1987, Num 10, pp 1931-1934 ; ref : 10 ref
- CODEN
- CMLTAG
- ISSN
- 0366-7022
- Domaine scientifique
- Chemistry; Atomic molecular physics
- Editeur
- Chemical Society of Japan, Tokyo
- Pays de publication
- Japan
- Type de document
- Article
- Langue
- English
- Mot clé (fr)
- Acétal Composé monocyclique Cétoéther Enol ester Enol éther Oxydation Réaction électrochimique Acétique acide Cycloheptadiène-4,6trione-1,2,3,bis-diméthylacétal-2,3 Cycloheptadiène-«3,6»trione-1,2,5,bis-diméthylacétal-2,5 Cycloheptatriénone(acétoxy-«4» diméthoxy-«2,7») Cycloheptatriénone(bromo-«2» méthoxy-«7») Cycloheptatriénone(diacétoxy méthoxy) Cycloheptatriénone(diméthoxy) Sulfurique acide
- Mot clé (en)
- Acetal Monocyclic compound Ketoether Enol ester Enol ether Oxidation Electrochemical reaction
- Mot clé (es)
- Acetal Compuesto monocíclico Cetoéter Enol ester Enol eter Oxidación Reacción electroquímica
- Classification
- Pascal
- 001 Sciences exactes et technologie / 001C Chimie / 001C03 Chimie organique / 001C03C Préparations et propriétés / 001C03C05 Cyclanes, terpènes, prostaglandines, stéroïdes
- Discipline
- Organic chemistry
- Provenance
- Inist-CNRS
- Base de données
- PASCAL
- Identifiant INIST
- 7751467
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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