Diastereoisomers with three neighbouring phenyl groups. IX: Relative configurations and conformations of 3-amino- and 3-methylamino-1,2,3-triphenyl-1-propyl chlorides
- Author
- KURTEVA, V. B1 ; LYAPOVA, M. J; POJARLIEFF, I. G
[1] Bulgarian acad. sci., inst. organic chemistry, Sofia 1040, Bulgaria - Source
Journal of chemical research. Synopses (Print). 1986, Num 11, pp 398-399 ; ref : 14 ref
- CODEN
- JRPSDC
- ISSN
- 0308-2342
- Scientific domain
- Organic chemistry; Atomic molecular physics
- Publisher
- Turpin, Letchworth
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Composé aliphatique saturé Configuration relative Conformation Constante couplage spin spin Etude expérimentale Solution chimique Spectre RMN Propane(amino-1 chloro-«3» triphényl-«1,2,3») Propane(chloro-«1» méthylamino-«3» triphényl-«1,2,3») Hydrogène 1
- Keyword (en)
- Saturated aliphatic compound Relative configuration Conformation Spin spin coupling constant Experimental study Chemical solution NMR spectrum
- Keyword (es)
- Compuesto alifático saturado Configuración relativa Conformacion Constante acoplamiento spin spin Estudio experimental Solución química Espectro de RMN
- Classification
- Pascal
- 001 Exact sciences and technology / 001B Physics / 001B30 Atomic and molecular physics / 001B30C Molecular properties and interactions with photons / 001B30C15 Properties of molecules and molecular ions / 001B30C15B General molecular conformation and symmetry; stereochemistry
- Discipline
- Atomic and molecular physics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 8245735
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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