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  4. Palladium-catalyzed enantioselective domino Heck-cyanation sequence: development and application to the total synthesis of esermethole and physostigmine
 
research article

Palladium-catalyzed enantioselective domino Heck-cyanation sequence: development and application to the total synthesis of esermethole and physostigmine

Pinto, Artur
•
Jia, Yanxing
•
Neuville, Luc
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2007
Chemistry--A European Journal

An efficient synthesis of functionalized 3-alkyl-3-cyanomethyl-2-oxindole by a palladium-catalyzed domino Heck-cyanation reaction has been developed. Reaction of ortho-iodoanilide with potassium ferro(II)cyanide in the presence of palladium acetate and sodium carbonate afforded oxindole derivs., e.g., I, in good to excellent yields. An enantioselective domino Heck-cyanation process has been developed for the first time using (S)-DIFLUORPHOS as a chiral supporting ligand, and an enantioselectivity of up to 79% ee in the enantiomerically enriched oxindole was obtained under optimized conditions. A concise total synthesis of (+-)-esermethole (II, R = Me) and (+-)-physostigmine (II, R = CONHMe), powerful inhibitors of acetyl- and butyryl-cholinesterase, is also described. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1002/chem.200601016
Author(s)
Pinto, Artur
Jia, Yanxing
Neuville, Luc
Zhu, Jieping  
Date Issued

2007

Published in
Chemistry--A European Journal
Volume

13

Issue

3

Start page

961

End page

967

Subjects

Arylation (Heck

•

intramol.; stereoselective prepn. of oxindole derivs. via palladium-phosphine-catalyzed asym. intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); Amides Role: RCT (Reactant)

•

RACT (Reactant or reagent) (aryl; prepn. of oxindole derivs. via palladium-catalyzed intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); Ligands Role: CAT (Catalyst use)

•

USES (Uses) (chiral; stereoselective prepn. of oxindole derivs. via palladium-phosphine-catalyzed asym. intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); Cyanation; Heck reaction catalysts; Stereoselective synthesis (stereoselective prepn. of oxindole derivs. via palladium-phosphine-catalyzed asym. intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide)

•

physostigmine prepn; esermethole prepn; oxindole asym prepn; aryl acrylamide Heck cyanation palladium chiral phosphine ligand

Note

CAN 146:337762

28-2

Heterocyclic Compounds (More Than One Hetero Atom)

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

Journal

written in English.

3375-31-3 (Palladium diacetate) Role: CAT (Catalyst use), USES (Uses) (prepn. of oxindole derivs. via palladium-catalyzed intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); 13943-58-3 (Potassium ferrocyanide); 102804-50-2; 122128-46-5; 154386-63-7; 929610-20-8; 929610-21-9; 929610-22-0; 929610-23-1; 929610-24-2; 929610-25-3; 929610-26-4; 929610-27-5; 929610-28-6 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of oxindole derivs. via palladium-catalyzed intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); 34944-03-1P; 136977-64-5P; 136977-87-2P; 176327-11-0P; 929610-29-7P; 929610-30-0P; 929610-31-1P; 929610-32-2P; 929610-33-3P; 929610-34-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of oxindole derivs. via palladium-catalyzed intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); 920-46-7; 18342-66-0; 191348-14-8 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of physostigmine via amidation of iodo(methoxy)aniline with metharyloyl chloride followed by methylation, palladium-catalyzed Heck-cyanation, reductive amination/cyclization, methylation, demethylation and esterification); 2291-51-2P; 46479-71-4P; 65131-82-0P ((+-)-Esermethole); 70354-71-1P; 929610-35-5P; 929610-36-6P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of physostigmine via amidation of iodo(methoxy)aniline with metharyloyl chloride followed by methylation, palladium-catalyzed Heck-cyanation, reductive amination/cyclization, methylation, demethylation and esterification); 69926-97-2P ((+-)-Physostigmine) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of physostigmine via amidation of iodo(methoxy)aniline with metharyloyl chloride followed by methylation, palladium-catalyzed Heck-cyanation, reductive amination/cyclization, methylation, demethylation and esterification); 32005-36-0 (Bis(dibenzylideneacetone)palladium); 445467-61-8; 503538-70-3 Role: CAT (Catalyst use), USES (Uses) (stereoselective prepn. of oxindole derivs. via palladium-phosphine-catalyzed asym. intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide); 131101-13-8P; 132620-31-6P; 685089-46-7P; 929610-37-7P Role: SPN (Synthetic preparation), PREP (Preparation) (stereoselective prepn. of oxindole derivs. via palladium-phosphine-catalyzed asym. intramol. Heck-cyanation of N-aryl acrylamides in presence of potassium ferrocyanide)

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/20.500.14299/58430
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