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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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