Synthesis of β-amino-α-hydroxy esters and β-amino-α-azido ester by sharpless asymmetric aminohydroxylation, byproducts analysis
- Author
- ZUOSHENG LIU; NIANCHUN MA; YANXING JIA; BOIS-CHOUSSY, Michèle; MALABARBA, Adriano; JIEPING ZHU
Institut de Chimie des Substances Naturelles, CNRS, 91198 Gif-sur-Yvette, France
Italy Research Center, Vicuron Pharmaceuticals, via R. Lepetit, 34, 21040 Gerenzano (VA), Italy - Source
Journal of organic chemistry. 2005, Vol 70, Num 7, pp 2847-2850, 4 p ; ref : 20 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)
- Amine Aminoester Azide Cétoester Ester Hydroxyester Oxydation Réaction chimique secondaire Synthèse asymétrique Synthèse chimique Aminohydroxylation Sharpless Propionique acide(3-t-butoxycarbonylamino-3-[3,5-diisopropoxy-4-méthoxy-phényl]-2-hydroxy) ester méthyle
- Keyword (en)
- Amine Aminoester Organic azide Ketoester Ester Hydroxyester Oxidation Side reaction Asymmetric synthesis Chemical synthesis
- Keyword (es)
- Amina Aminoester Azida orgánica Cetoester Ester Hidroxiester Oxidación Reacción química secundaria Síntesis asimétrica Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16639791
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/jo047772o 
https://dx.doi.org/10.1021/jo047772o
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