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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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