AlCl3-mediated regioselective migration of a methoxy group of N-methoxy-N-phenylamides to the ortho position of the phenyl ring
- Author
- KIKUGAWA, Y1 ; SHIMADA, M
[1] Josai univ., fac. pharmaceutical sci., Sakado Saitama 350-02, Japan - Source
Journal of the Chemical Society. Chemical communications. 1989, Num 19, pp 1450-1451 ; ref : 6 ref
- CODEN
- JCCCAT
- ISSN
- 0022-4936
- Scientific domain
- Chemistry; Crystallography; Atomic molecular physics
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide carbohydroxamique Aluminium III Chlorure Carboxamide Composé aliphatique Composé benzénique Composé vinylique Décomposition chimique Intermédiaire réaction Paire ion Régiosélectivité Transposition chimique Cinnamique acide,méthoxy-«2p» phénylamide Cinnamohydroxamique acide(«O»-méthyl «N»-phényl) Ethane(dichloro)
- Keyword (en)
- Carbohydroxamic acid Aluminium III Chlorides Carboxamide Aliphatic compound Benzenic compound Vinylic compound Chemical decomposition Reaction intermediate Ion pair Regioselectivity Chemical rearrangement
- Keyword (es)
- Acido carbohidroxámico Aluminio III Carboxamida Compuesto alifático Compuesto bencénico Compuesto vinílico Descomposición química Intermediario reacción Par ión Regioselectividad Transposición química
- 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
- 6658297
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
10.1039/c39890001450 
https://dx.doi.org/10.1039/c39890001450
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