3-(2-Alken-1-one-2-yl)indoles through the palladium-catalyzed reaction of 2-alkynyltrifluoroacetanilides with cyclic α-iodoenones
- Author
- ARCADI, Antonio1 ; CIANCI, Roberto1 ; FERRARA, Giovanni1 ; MARINELLI, Fabio1
[1] Dipartimento di Chimica, Ingegneria Chimica e Materiali, Università dell'Aquila, via Vetoio, 67100 L'Aquila, Italy - Source
Tetrahedron (Oxford. Print). 2010, Vol 66, Num 13 ; 2228, 2378-2383 [7 p.]
- CODEN
- TETRAB
- ISSN
- 0040-4020
- Scientific domain
- Organic chemistry
- Publisher
- Elsevier, Kidlington
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Acétanilide Arsenic composé organique Carbonate de césium Complexe de palladium Composé cyclique Composé éthylénique Dérivé de l'indole Electrophile Enone Hétérocycle azote Iode Composé organique Ligand Réaction catalytique Synthèse chimique Triphénylarsine
- Keyword (en)
- Acetanilide Organic arsenic compounds Cesium carbonate Palladium complex Cyclic compound Ethylenic compound Indole derivatives Electrophile Enone Nitrogen heterocycle Iodine Organic compounds Ligand Catalytic reaction Chemical synthesis
- Keyword (es)
- Acetanilida Cesio carbonato Paladio complejo Compuesto cíclico Compuesto etilénico Indol derivado Electrófilo Enona Heterociclo nitrógeno Iodo Compuesto orgánico Ligando Reacción catalítica Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 22611505
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
10.1016/j.tet.2010.01.096 
https://dx.doi.org/10.1016/j.tet.2010.01.096
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