Synthesis and characterization of highly conjugated, chiral bridging ligands
- Author
- SAUERS, Angela L1 ; HO, Douglas M1 ; BERNHARD, Stefan1
[1] Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States - Source
Journal of organic chemistry. 2004, Vol 69, Num 25, pp 8910-8915, 6 p
- 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)
- Activité optique Composé chiral Condensation chimique Cycle 6 chaînons Dégradation oxydante Enantiosélectivité Hétérocycle azote Propriété optique Pyrazine dérivé Spectrométrie CD Synthèse organique Pyrazine(2,3,5,6-tétrakis[2-pyridyl])
- Keyword (en)
- Optical activity Chiral compound Condensation reaction Six membered ring Oxidative degradation Enantioselectivity Nitrogen heterocycle Optical properties Pyrazine derivatives Circular dichroism spectrometry Organic synthesis
- Keyword (es)
- Actividad óptica Compuesto quiral Condensación química Ciclo 6 eslabones Degradación oxidante Enantioselectividad Heterociclo nitrógeno Propiedad óptica Pirazina derivado Espectrometría CD Síntesis orgánica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06C Heterocyclic compounds with several n hetero atoms in the same ring, in separated rings or in fused rings
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 16322918
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/jo048515m 
https://dx.doi.org/10.1021/jo048515m
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