An efficient route to all stereoisomeric enantiopure 6-amino-3-alkyl-3- azabicyclo[3.2.1]octane-6-carboxylic acids

Journal of Organic Chemistry

Volumn 72, Issue 25, 2007, Pages 9811-9814

  Gelmi, Maria Luisa ^a   Cattaneo, Cristian ^a   Pellegrino, Sara ^a   Clerici, Francesca ^a   Montali, Marina ^b   Martini, Claudia ^b  

^a UNIVERSITY OF MILAN   (Italy)

^b UNIVERSITY OF PISA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; ANILINE; BIOACTIVITY; CHIRALITY; HYDROGENOLYSIS; SYNTHESIS (CHEMICAL);

GABA RECEPTOR; GRAM SCALE; PHENYLETHYLAMINE; STEREOISOMERS;

CARBOXYLIC ACIDS;

4 AMINOBUTYRIC ACID RECEPTOR; CARBOXYLIC ACID DERIVATIVE; NITROGEN; PHENETHYLAMINE DERIVATIVE;

ALKYLATION; ARTICLE; BIOLOGICAL ACTIVITY; CHIRALITY; DEPROTECTION REACTION; HYDROGENOLYSIS; STEREOISOMERISM;

CARBOXYLIC ACIDS; MOLECULAR STRUCTURE; STEREOISOMERISM; TROPANES;

EID: 36849002377     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo7019702     Document Type: Article

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