Thermal cycloaddition of N-arylmaleimides to phenols: the convenient synthesis of bicyclo [2.2.2]oct-2-en-5-one and tricyclo[3.3.0.0.2,8]octan-2-one derivatives from phenols
- Author
- BRYCE-SMITH, D1 ; GILBERT, A; MCCOLL, I. S; DREW, M. G. B; YIANNI, P
[1] Univ. Reading, dep. chemistry, Reading Berks. RG6 2AD, United Kingdom - Source
Journal of the Chemical Society. Perkin transactions. I. 1987, Num 5, pp 1147-1151 ; ref : 15 ref
- CODEN
- JCPRB4
- ISSN
- 0300-922X
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Royal Society of Chemistry, Cambridge
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Composé bicyclique Cycle 5 chaînons Cycloaddition Cétoester Diester Hétérocycle azote Imide Photolyse UV Phénols Réaction thermique Bicyclo [«2.2.2»] octène-«5»dicarboxylique-2,3 acide(oxo-«7») ester diméthyle Maléimide(N-[diméthyl-«2,6» phényl]) Maléimide(N-aryl) Phénol(méthoxy-«4») Triacyclooctane dérivé «p»-Crésol
- Keyword (en)
- Bicyclic compound Five membered ring Cycloaddition Ketoester Diester Nitrogen heterocycle Imide Ultraviolet photolysis Phenols Thermal reaction
- Keyword (es)
- Compuesto bicíclico Ciclo 5 eslabones Cicloadición Cetoester Diester Heterociclo nitrógeno Imida Fotolisis UV Fenoles Reacción térmica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7408213
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/p19870001147 
https://dx.doi.org/10.1039/p19870001147
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