An Efficient Route to All Stereoisomeric Enantiopure 6-Amino-3-alkyl-3-azabicyclo[3.2.1]octane-6-carboxylic Acids
- Author
- GELMI, Maria Luisa1 ; CATTANEO, Cristian1 ; PELLEGRINO, Sara1 ; CLERICI, Francesca1 ; MONTALI, Marina2 ; MARTINI, Claudia2
[1] Istituto di Chimica Organica A. Marchesini, Facoltà di Farmacia, Università di Milano, Via Venezian 21, 20133 Milano, Italy
[2] Dipartimento di Psichiatria, Neurobiologia, Farmacologia e Biotecnologie, Università di Pisa, Via Bonanno 6, 56126 Pisa, Italy - Source
Journal of organic chemistry. 2007, Vol 72, Num 25, pp 9811-9814, 4 p ; ref : 11 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)
- Acide carboxylique Activité biologique Alkylation Amine Aminoacide Chiralité Déprotection GABA Hydrogénolyse Hétérocycle azote Stéréoisomère Synthèse chimique Azabicyclooctane dérivé Ethylamine(1-phényl)
- Keyword (en)
- Carboxylic acid Biological activity Alkylation Amine Aminoacid Chirality Deprotection GABA Hydrogenolysis Nitrogen heterocycle Stereoisomer Chemical synthesis
- Keyword (es)
- Acido carboxílico Actividad biológica Alquilación Amina Aminoácido Quiralidad Desprotección GABA Hidrogenolisis Heterociclo nitrógeno Estereoisómero 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
- 19895990
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/jo7019702 
https://dx.doi.org/10.1021/jo7019702
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