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Stereodynamics and Conformational Chirality of the Atropisomers of Ditolyl Anthrones and Anthraquinone

Author
LUNAZZI, Lodovico1 ; MANCINELLI, Michele1 ; MAZZANTI, Andrea1
[1] Department of Organic Chemistry A. Mangini, University of Bologna, Viale Risorgimento 4, Bologna 40136, Italy
Source

Journal of organic chemistry. 2008, Vol 73, Num 14, pp 5354-5359, 6 p ; ref : 30 ref

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)
Anthrone Atropisomérie Barrière énergie Chiralité Composé aromatique Conformation Diffraction RX Dérivé de l'anthracène Dérivé de l'anthraquinone Effet température Etude expérimentale Interconversion Méthode fonctionnelle densité Quinone Simulation Spectrométrie RMN Structure cristalline Structure moléculaire Stéréoisomère anti Stéréoisomère syn Température ambiante
Keyword (en)
Atropoisomerism Energy barrier Chirality Aromatic compound Conformation X ray diffraction Anthracene derivatives Anthraquinone derivatives Temperature effect Experimental study Interconversion Density functional method Quinone Simulation NMR spectrometry Crystalline structure Molecular structure Anti stereoisomer Syn stereoisomer Room temperature
Keyword (es)
Atropoisomería Barrera energía Quiralidad Compuesto aromático Conformación Difracción RX Antraceno derivado Antraquinona derivado Efecto temperatura Estudio experimental Interconversión Quinona Simulación Espectrometría RMN Estructura cristalina Estructura molecular Estereoisómero anti Estereoisómero sin Temperatura ambiente
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
20499033

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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