A simplified synthesis of 2,3,5,6-tetrafluorophenyl 2-(2-nitroimidazol-1-yl) acetate
- Author
- WILSON, Hanna1
[1] Imaging Research Solutions Ltd., Cyclotron Building, Hammersmith Hospital, Du Cane Road, London W12 0NN, United Kingdom - Source
Journal of labelled compounds & radiopharmaceuticals. 2003, Vol 46, Num 6, pp 511-513, 3 p ; ref : 6 ref
- ISSN
- 0362-4803
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry; Pharmacology drugs
- Publisher
- Wiley, Chichester
/
Wiley, New York, NY
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Composé nitro Copulation chimique Cycle 5 chaînons Estérification Fluor Composé organique Halogénophénols Hétérocycle azote Imidazole dérivé Synthèse chimique Carbodiimide(dicyclohexyl) Etanidazole dérivé Imidazole-1-acétique acide(2-nitro) ester tétrafluorophényle Imidazole-1-acétique acide(2-nitro) Phénol(2,3,5,6-tétrafluoro)
- Keyword (en)
- Nitro compound Chemical coupling Five membered ring Esterification Fluorine Organic compounds Halophenols Nitrogen heterocycle Imidazole derivatives Chemical synthesis
- Keyword (es)
- Compuesto nitro Copulación química Ciclo 5 eslabones Esterificación Fluor Compuesto orgánico Halofenoles Heterociclo nitrógeno Imidazol derivado Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 14829619
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
10.1002/jlcr.691 
https://dx.doi.org/10.1002/jlcr.691
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