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  4. Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles
 
research article

Palladium-catalyzed domino Heck/cyanation: synthesis of 3-cyanomethyloxindoles and their conversion to spirooxoindoles

Jaegli, Stephanie
•
Vors, Jean-Pierre
•
Neuville, Luc
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2010
Tetrahedron

3'-Alkyl-3-cyanomethyloxindoles, prepd. by a palladium-catalyzed domino Heck/cyanation, were efficiently converted to spiropyrrolidinyl-, spiropiperidinyl- and spirocyclopropyl-oxindoles. The so-obtained spirooxindoles bearing three diversity points were further functionalized via selective N-acylation, N-alkylation, N-sulfonylation, SNAr reaction and Buchwald-Hartwig N-arylation reaction to reach diverse set of heterocycles. [on SciFinder (R)]

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Type
research article
DOI
10.1016/j.tet.2010.09.056
Author(s)
Jaegli, Stephanie
Vors, Jean-Pierre
Neuville, Luc
Zhu, Jieping  
Date Issued

2010

Published in
Tetrahedron
Volume

66

Issue

46

Start page

8911

End page

8921

Note

27, Heterocyclic Compounds (One Hetero Atom), Centre de Recherche de Gif,Institut de Chimie des Substances Naturelles, CNRS,Gif-sur-Yvette,Fr., Journal, 0040-4020, written in English.

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/20.500.14299/58595
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