The synthesis of 3-(4-aminotetrafluorophenyl)-3-ethylpiperidine-2,6-dione: a fluorinated derivative of aminoglutethimide
- Author
- PLEVEY, R. G1 ; SAMPSON, P
[1] Univ. Birmingham, dep. chemistry, Birmingham B15 2TT, United Kingdom - Source
Journal of the Chemical Society. Perkin transactions. I. 1987, Num 10, pp 2129-2136 ; 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)
- Activité biologique Ammoniac Cholesterol monooxygenase(side-chain cleaving) Cycle 6 chaînons Hétérocycle azote Imide Inhibiteur enzyme Oestrogen synthase Substitution nucléophile Aminoglutéthimide dérivé Pipéridinedione-2,6([amino-4p tétrafluoro phényl]-«3» éthyl-«3») Pipéridinedione-2,6(éthyl-«3» perfluorophényl-«3»)
- Keyword (en)
- Biological activity Ammonia Cholesterol monooxygenase(side-chain cleaving) Six membered ring Nitrogen heterocycle Imide Enzyme inhibitor Oestrogen synthase Nucleophilic substitution
- Keyword (es)
- Actividad biológica Amoníaco Cholesterol monooxygenase(side-chain cleaving) Ciclo 6 eslabones Heterociclo nitrógeno Imida Inhibidor enzima Oestrogen synthase Substitución nucleófila
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7551811
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/p19870002129 
https://dx.doi.org/10.1039/p19870002129
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