A mechanistic approach to the reaction between imines and sodium hydrogen telluride
- Author
- BARTON, D. H. R1 ; BOHE, L; LUSINCHI, X
[1] CNRS, inst. chimie substances naturelles, Gif-sur-Yvette 91198, France - Source
Tetrahedron letters. 1988, Vol 29, Num 21, pp 2571-2574 ; ref : 13 ref
- CODEN
- TELEAY
- ISSN
- 0040-4039
- Scientific domain
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Publisher
- Elsevier, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Addition nucléophile Amine secondaire Aminonitrile Composé benzénique Hydrogène Tellurure Imine Réduction chimique Acétophénone,méthylimine Amine(benzhydryl méthyl) Amine(méthoxy-«4» benzyl méthyl) Benzonitrile(méthylaminométhyl-4) Benzonitrile(méthyliminométhyl-«4») Toluène(méthoxy-«4») «p»-Anisaldéhyde,méthylimine
- Keyword (en)
- Nucleophilic addition Secondary amine Aminonitrile Benzenic compound Hydrogen Tellurides Imine Chemical reduction
- Keyword (es)
- Adición nucleófila Amina secundaria Aminonitrilo Compuesto bencénico Hidrógeno Imina Reducción química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03B Reactivity and mechanisms / 001C03B02 Kinetics and mechanisms
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 7190481
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
10.1016/S0040-4039(00)86114-6 
https://dx.doi.org/10.1016/S0040-4039(00)86114-6
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