Para fluorination by N-fluorobis[(trifluoromethy)sulfonyl]imide : synthesis of 10β-fluoro-3-oxo-1,4-estradiene steroids
- Author
- PENNINGTON, W. T; RESNATI, G; DESMARTEAU, D. D
Clemson univ., Howard L. Hunter chemistry, Clemson SC 29629-1905, United States - Source
Journal of organic chemistry. 1992, Vol 57, Num 5, pp 1536-1539 ; ref : 42 ref
- CODEN
- JOCEAH
- ISSN
- 0022-3263
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acylate Acétique acide Chloroforme Composé aromatique Diénone Effet solvant Fluoration Halogénocétone Halogénophénols Imide Phénols Stéroïde Sélectivité Méthanesulfonique acide(trifluoro) [fluoro trifluoromésyl]amide Oestra-1,3,5(10)-triène-3,17β-diol 17β-propionate Oestra-1,3,5(10)-triène-3,17β-diol(4-fluoro)-17β-propionate Oestra-1,4-dièn-3-one(10β-fluoro-17-propionyloxy)
- Keyword (en)
- Acylate Acetic acid Chloroform Aromatic compound Dienone Solvent effect Fluorination Haloketone Halophenols Imide Phenols Steroid Selectivity
- Keyword (es)
- Acilato Acético ácido Compuesto aromático Dienona Efecto solvente Fluoración Halocetona Halofenoles Imida Fenoles Esteroide Selectividad
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05D Steroids
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5170046
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
10.1021/jo00031a038 
https://dx.doi.org/10.1021/jo00031a038
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