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  4. Synthesis of 3-(Diarylmethylenyl)oxindole by a Palladium-Catalyzed Domino Carbopalladation/C-H Activation/C-C Bond-Forming Process
 
research article

Synthesis of 3-(Diarylmethylenyl)oxindole by a Palladium-Catalyzed Domino Carbopalladation/C-H Activation/C-C Bond-Forming Process

Pinto, Artur
•
Neuville, Luc
•
Retailleau, Pascal
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2006
Organic Letters

A highly efficient palladium-catalyzed synthesis of unsym. substituted 3-(diarylmethylenyl)indolinones from readily accessible starting materials is developed. The domino reaction involves a sequence of intermol. carbopalladation, C-H activation, and C-C bond formation. A plausible mechanistic pathway for the reaction is discussed on the basis of the kinetic isotope effect [KH/KD (intermol.) = 1, KH/KD (intramol.) = 2.7] as well as the electronic effect. [on SciFinder (R)]

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Type
research article
DOI
10.1021/ol062022h
Author(s)
Pinto, Artur
Neuville, Luc
Retailleau, Pascal
Zhu, Jieping  
Date Issued

2006

Published in
Organic Letters
Volume

8

Issue

21

Start page

4927

End page

4930

Subjects

diarylmethylenylindolinone prepn propiolanilide iodoarene

Note

CAN 145:489084

27-11

Heterocyclic Compounds (One Hetero Atom)

Institut de Chimie des Substances Naturelles,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

3375-31-3 (Palladium(II) acetate) Role: CAT (Catalyst use), USES (Uses) (prepn. of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process); 914785-51-6P Role: PRP (Properties), SPN (Synthetic preparation), PREP (Preparation) (prepn. of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process); 529-28-2 (2-Iodoanisole); 591-50-4 (Iodobenzene); 609-73-4 (1-Iodo-2-nitrobenzene); 615-37-2 (2-Iodotoluene); 637-44-5 (Phenylpropiolic acid); 637-87-6; 766-85-8 (3-Iodoanisole); 3422-01-3 (N-tert.-Butoxycarbonylaniline); 14545-23-4 (Heptadeuteroaniline); 90585-26-5 (N-(2-Iodophenyl)-N-methylacetamide); 94298-51-8; 111054-32-1; 914785-45-8; 914785-46-9; 914785-47-0; 914785-48-1; 914785-49-2; 914785-50-5; 914785-71-0 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process); 914785-66-3P; 914785-67-4P; 914785-68-5P; 914785-69-6P; 918958-93-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process); 914785-52-7P; 914785-53-8P; 914785-54-9P; 914785-55-0P; 914785-56-1P; 914785-57-2P; 914785-58-3P; 914785-59-4P; 914785-60-7P; 914785-61-8P; 914785-62-9P; 914785-63-0P; 914785-64-1P; 914785-65-2P; 914785-72-1P; 914785-73-2P; 914785-74-3P; 914785-75-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process)

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/20.500.14299/58441
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