An Enantioselective Synthetic Route to cis-2,4-Disubstituted and 2,4-Bridged Piperidines
- Author
- AMAT, Mercedes1 ; PEREZ, Maria1 ; MINAGLIA, Annamaria T1 ; BOSCH, Joan1
[1] Laboratory of Organic Chemistry, Faculty of Pharmacy, and Institute of Biomedicine (IBUB), University of Barcelona, 08028 Barcelona, Spain - Source
Journal of organic chemistry. 2008, Vol 73, Num 17, pp 6920-6923, 4 p
- 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 chimique Composé insaturé Cuivre Composé organique Dérivé de la pipéridine Enantiosélectivité Hétérocycle azote Lactame Stéréosélectivité Synthèse chimique 1,3-Oxazolo[3,2-a]pyridine dérivé 2-Azabicyclo[3.3.1]nonane dérivé Ethanolamine(2-phényl)
- Keyword (en)
- Addition reaction Unsaturated compound Copper Organic compounds Piperidine derivatives Enantioselectivity Nitrogen heterocycle Lactam Stereoselectivity Chemical synthesis
- Keyword (es)
- Adición química Compuesto insaturado Cobre Compuesto orgánico Piperidina derivado Enantioselectividad Heterociclo nitrógeno Lactamo Estereoselectividad 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
- 20623073
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/jo801172b 
https://dx.doi.org/10.1021/jo801172b
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