Stereochemical control of reductions. 9. Haptophilicity studies with 1,1-disubstituted 2-methyleneacenaphthenes
- Author
- THOMPSON, Hugh W1 ; RASHID, Shaker Y1
[1] Carl A. Olson Memorial Laboratories, Department of Chemistry, Rutgers University, Newark, New Jersey 07102, United States - Source
Journal of organic chemistry. 2002, Vol 67, Num 9, pp 2813-2825
- 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)
- Acénaphtène dérivé Carbone Constante diélectrique Effet substituant Epimère Hydrogénation Palladium Réaction catalytique Réduction chimique Solvant Stéréochimie Acénaphtène-1-carbonitrile(1,2-diméthyl) Acénaphtène-1-carbonitrile(1-méthyl-2-méthylène) Haptophilicité Propionique acide(2-[1-naphtyl]) Métal transition
- Keyword (en)
- Acenaphthene derivatives Carbon Permittivity Substituent effect Epimer Hydrogenation Palladium Catalytic reaction Chemical reduction Solvent Stereochemistry Transition metal
- Keyword (es)
- Acenafteno derivado Carbono Constante dieléctrica Efecto sustituyente Epímero Hidrogenación Paladio Reacción catalítica Reducción química Solvente Estereoquímica Metal transición
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C04 Condensed benzenic and aromatic compounds
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 14189477
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
10.1021/jo010633b 
https://dx.doi.org/10.1021/jo010633b
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