AlCl3-Mediated Direct Carbon-Carbon Bond-Forming Reaction of a-Hydroxyketene-S,S-acetals with Arenes and Synthesis of 3,4-Disubstituted Dihydrocoumarin Derivatives
- Author
- PIAO, Cheng-Ri1 ; ZHAO, Yu-Long1 ; HAN, Xiao-Dan1 ; QUN LIU1
[1] Department of Chemistry, Northeast Normal University, Changchun, 130024, China - Source
Journal of organic chemistry. 2008, Vol 73, Num 6, pp 2264-2269, 6 p ; ref : 22 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)
- Acétal Alcool Aluminium III Chlorure Annélation Composé aromatique Condition opératoire modérée Copulation chimique Cétènes Dérivé de la coumarine Hétérocycle oxygène Lactone Phénols Réaction Friedel Crafts Réaction intramoléculaire Synthèse chimique Benzo[f]chromène dérivé Composé acyclique
- Keyword (en)
- Acetal Alcohol Aluminium III Chlorides Annelation Aromatic compound Mild operating conditions Chemical coupling Ketenes Coumarine derivatives Oxygen heterocycle Lactone Phenols Friedel Crafts reaction Intramolecular reaction Chemical synthesis
- Keyword (es)
- Acetal Alcohol Aluminio III Cloruro Anillación Compuesto aromático Condición operatoria moderada Copulación química Cetenas Heterociclo oxígeno Lactona Fenoles Reacción Friedel Crafts Reacción intramolecular Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06A Heterocyclic compounds with o, s, se, te hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 20188787
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/jo702414y 
https://dx.doi.org/10.1021/jo702414y
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