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Stereoselective synthesis of 2-amino-3-fluoro bicyclo[3.1.0]hexane-2,6-dicarboxylic acid

Author
PEDREGAL, Concepcion1 ; PROWSE, William2
[1] Centro de Investigación Lilly, SA, Avda. de la Industria, 30, 28108, Alcobendas, Madrid, Spain
[2] Lilly Research Centre Ltd., Windlesham, Surrey GU20 6PH, United Kingdom
Source

Bioorganic & medicinal chemistry. 2002, Vol 10, Num 2, pp 433-436

ISSN
0968-0896
Scientific domain
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Publisher
Elsevier Science, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Azide Catalyseur sur support Composé bicyclique Diacide carboxylique Ethanol Fluor Composé organique Hydrogénation Palladium Racémique Réaction catalytique Sodium Azoture Stéréosélectivité Synthèse chimique α-Aminoacide Bicyclo[3.1.0]hexane-2,6-dicarboxylique acide(2-amino-3-fluoro) Bicyclo[3.1.0]hexane-6-carboxylique acide(3-fluoro-2-hydroxy-2-trichlorométhyl) ester éthyle DBU LY 354740
Keyword (en)
Organic azide Supported catalyst Bicyclic compound Dicarboxylic acid Ethanol Fluorine Organic compounds Hydrogenation Palladium Racemic Catalytic reaction Sodium Azides Stereoselectivity Chemical synthesis α-Aminoacid
Keyword (es)
Azida orgánica Catalizador sobre soporte Compuesto bicíclico Diácido carboxílico Etanol Fluor Compuesto orgánico Hidrogenación Paladio Racémico Reacción catalítica Sodio Azoturo Estereoselectividad Síntesis química α-Aminoácido
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
13395829

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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