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  4. Diester-Substituted Aminocyclopropanes: Synthesis and Use in [3+2]-Annulation Reactions
 
research article

Diester-Substituted Aminocyclopropanes: Synthesis and Use in [3+2]-Annulation Reactions

Serrano, Eloisa  
•
De Nanteuil, Florian  
•
Waser, Jerome  
2014
Synlett

In this Letter, we describe the synthesis of new donor-acceptor substituted cyclopropanes bearing various imido groups and their use in [3+2]-annulation reactions. A sequence of palladium-catalyzed vinylation and rhodium-catalyzed cyclopropanation gave access to the required cyclopropanes in only two steps and high overall yields. The obtained compounds were used successfully in the tin-catalyzed [3+2] annulation with enol ethers to give cyclopentylamine derivatives in 22-95% yield.

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Type
research article
DOI
10.1055/s-0034-1378512
Web of Science ID

WOS:000342570400014

Author(s)
Serrano, Eloisa  
De Nanteuil, Florian  
Waser, Jerome  
Date Issued

2014

Publisher

Georg Thieme Verlag

Published in
Synlett
Volume

25

Issue

16

Start page

2285

End page

2288

Subjects

annulation

•

carbocycles

•

homogenous catalysis

•

nitrogen

•

ring opening

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
Available on Infoscience
November 13, 2014
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/108691
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