A practical and efficient method for the construction of the biphenyl framework; nucleophilic aromatic substitution on 2-methoxybenzoates with aryl grignard reagents
- Author
- HATTORI, T; SUZUKI, T; MIYANO, S
Tohoku univ., fac. eng., dep. biochemistry eng., Aoba-ku, Sendai 980, Japan - Source
Journal of the Chemical Society. Chemical communications. 1991, Num 19, pp 1375-1376 ; ref : 8 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)
- Composé benzénique Composé tricyclique Hétérocycle oxygène Phénols Réactif Grignard Substitution aromatique Substitution nucléophile Benzoïque acide(2-méthoxy-4-méthyl) ester aryle Biphényle-2-carboxylique acide ester aryle Cannabinol Dibenzo [b.d] pyrane dérivé Magnésium(aryl) bromure o-Anisique acide ester aryle
- Keyword (en)
- Benzenic compound Tricyclic compound Oxygen heterocycle Phenols Grignard reagent Aromatic substitution Nucleophilic substitution
- Keyword (es)
- Compuesto bencénico Compuesto tricíclico Heterociclo oxígeno Fenoles Reactivo Grignard Sustitución aromática Substitución nucleófila
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03A General
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5388123
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/c39910001375 
https://dx.doi.org/10.1039/c39910001375
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