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  4. Palladium-Catalyzed Carbo-Heterofunctionalization of Alkenes for the Synthesis of Oxindoles and Spirooxindoles
 
research article

Palladium-Catalyzed Carbo-Heterofunctionalization of Alkenes for the Synthesis of Oxindoles and Spirooxindoles

Jaegli, Stephanie
•
Dufour, Jeremy
•
Wei, Hai-long
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2010
Organic Letters

A palladium-catalyzed oxidative carbo-heterofunctionalization of aniline derivs. involving concomitant direct C-H functionalization and C-X bond formation was developed. By simply changing the reaction conditions (solvent and catalyst), either 3,3'-disubstituted oxindole or spirooxindole was accessible from the same starting material. E.g., reaction of acrylanilide I in presence of Pd(OAc)2 and PhI(OAc)2 gave 54% oxindole II. [on SciFinder (R)]

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Type
research article
DOI
10.1021/ol101778c
Author(s)
Jaegli, Stephanie
Dufour, Jeremy
Wei, Hai-long
Piou, Tiffany
Duan, Xin-Hua
Vors, Jean-Pierre
Neuville, Luc
Zhu, Jieping  
Date Issued

2010

Published in
Organic Letters
Volume

12

Issue

20

Start page

4498

End page

4501

Subjects

Acetoxylation

•

Acetoxylation catalysts

•

Cyclization

•

Cyclization catalysts

•

Spirocyclization

•

Spirocyclization catalysts (palladium-catalyzed oxidative carbo-heterofunctionalization of acrylanilides for the synthesis of oxindoles and spirooxindoles)

•

Anilides Role: RCT (Reactant)

•

RACT (Reactant or reagent) (palladium-catalyzed oxidative carbo-heterofunctionalization of acrylanilides for the synthesis of oxindoles and spirooxindoles)

•

palladium catalyst oxidative cyclization spirocyclization acetoxylation acrylanilide

•

oxindole spirooxindole prepn

Note

CAN 153:505623, 27-20, Heterocyclic Compounds (One Hetero Atom), Institut de Chimie des Substances Naturelles,Centre de Recherche de Gif, CNRS,Gif-sur-Yvette,Fr., Journal, 1523-7060, written in English., 3375-31-3; 7647-10-1 (Palladium chloride (PdCl2) Role: CAT (Catalyst use), USES (Uses) (palladium-catalyzed oxidative carbo-heterofunctionalization of acrylanilides for the synthesis of oxindoles and spirooxindoles); 10579-60-9; 15796-89-1; 74480-63-0; 85576-99-4; 200128-36-5; 294642-84-5; 860426-07-9; 1247767-81-2; 1247767-86-7; 1247767-87-8; 1247767-91-4; 1247767-93-6; 1247767-99-2; 1247768-01-9; 1247768-03-1; 1247768-05-3; 1247768-51-9 Role: RCT (Reactant), RACT (Reactant or reagent) (palladium-catalyzed oxidative carbo-heterofunctionalization of acrylanilides for the synthesis of oxindoles and spirooxindoles); 3240-34-4 ((Diacetoxyiodo)benzene) Role: RGT (Reagent), RACT (Reactant or reagent) (palladium-catalyzed oxidative carbo-heterofunctionalization of acrylanilides for the synthesis of oxindoles and spirooxindoles); 1234787-48-4P; 1234787-62-2P; 1247768-09-7P; 1247768-11-1P; 1247768-12-2P; 1247768-16-6P; 1247768-18-8P; 1247768-20-2P; 1247768-23-5P; 1247768-24-6P; 1247768-28-0P; 1247768-34-8P; 1247768-35-9P; 1247768-40-6P; 1247768-41-7P; 1247768-42-8P; 1247768-46-2P; 1247768-48-4P; 1247768-49-5P; 1247768-50-8P; 1247768-55-3P Role: SPN (Synthetic preparation), PREP (Preparation) (palladium-catalyzed oxidative carbo-heterofunctionalization of acrylanilides for the synthesis of oxindoles and spirooxindoles)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58594
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