An Efficient Method for the Synthesis of Nitropiperidones
- Author
- GARCIA RUANO, José Luis1 ; DE HARO, Teresa1 ; SINGH, Rajinder1 ; CID, M. Belén1
[1] Departamento de Quimica Orgânica, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain - Source
Journal of organic chemistry. 2008, Vol 73, Num 3, pp 1150-1153, 4 p ; ref : 27 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)
- Addition Michaël Amine Chromatographie Composé insaturé Composé nitro Condition opératoire modérée Cyclisation Dérivé de la pipéridinone Ester Etude expérimentale Hydrolyse Nitramine Purification Sulfoxyde Synthèse chimique
- Keyword (en)
- Michael addition Amine Chromatography Unsaturated compound Nitro compound Mild operating conditions Cyclization Piperidone derivatives Ester Experimental study Hydrolysis Nitramine Purification Sulfoxide Chemical synthesis
- Keyword (es)
- Adición Michael Amina Cromatografía Compuesto insaturado Compuesto nitro Condición operatoria moderada Ciclización Ester Estudio experimental Hidrólisis Nitramina Purificación Sulfóxido Síntesis química
- 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
- 20047536
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/jo702130a 
https://dx.doi.org/10.1021/jo702130a
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