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
- Author
- 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
- Scientific domain
- Chemistry; Atomic molecular physics
- Publisher
- Chemical Society of Japan, Tokyo
- Publication country
- Japan
- Document type
- Article
- Language
- English
- Keyword (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
- Keyword (en)
- Acetal Monocyclic compound Ketoether Enol ester Enol ether Oxidation Electrochemical reaction
- Keyword (es)
- Acetal Compuesto monocíclico Cetoéter Enol ester Enol eter Oxidación Reacción electroquímica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 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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DOI
10.1246/cl.1987.1931 
https://dx.doi.org/10.1246/cl.1987.1931
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