Stereoselective synthesis of α,β-diamino nitriles from amino acids
- Author
- REETZ, M. T1 ; HÜBEL, M1 ; JAEGER, R; SCHWICKARDI, R1 ; GODDARD, R1
[1] Max-Planck-Inst. Kohlenforschung, 45470 Mülheim/Ruhr, Germany - Source
Synthesis (Stuttgart). 1994, Num 7, pp 733-738 ; ref : 25 ref
- CODEN
- SYNTBF
- ISSN
- 0039-7881
- Scientific domain
- Organic chemistry
- Publisher
- Thieme, New York, NY
/
Thieme, Stuttgart
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acide Lewis Addition chimique Aldimine Aminoaldéhyde Aminonitrile Catalyse acide Composé aliphatique saturé Diamine Norvaline Stéréosélectivité α-Aminoacide Butanal(2-dibenzylamino) tosylimine Silane(cyano triméthyl) Valéronitrile(3-dibenzylamino-4-méthyl-2-tosylamino)
- Keyword (en)
- Lewis acid Addition reaction Aldimine Aminoaldehyde Aminonitrile Acid catalysis Saturated aliphatic compound Diamine Norvaline Stereoselectivity α-Aminoacid
- Keyword (es)
- Acido Lewis Adición química Aldimina Aminoaldehído Aminonitrilo Catálisis ácida Compuesto alifático saturado Diamina Norvalina Estereoselectividad α-Aminoácido
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C02 Aliphatic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4191564
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
10.1055/s-1994-25559 
https://dx.doi.org/10.1055/s-1994-25559
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