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  4. Ruthenium-Catalyzed Synthesis of 1,5-Dichlorides by Sequential Intermolecular Kharasch Reactions
 
research article

Ruthenium-Catalyzed Synthesis of 1,5-Dichlorides by Sequential Intermolecular Kharasch Reactions

Thommes, Katrin  
•
Fernandez-Zumel, Mariano Alfonso  
•
Buron, Charlotte
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2011
European Journal of Organic Chemistry

Sequential intermolecular atom transfer radical addition reactions of activated dichlorides Cl2CRR′ (R = CN, CO2Et, R′ = H, CN, CO2Et) with two olefins catalyzed by [Cp*RuCl2(PPh3)] in the presence Mg allow the synthesis of linear 1,5-dichlorides. Different olefins can be employed in the first and in the second addition reaction. The reaction products are interesting synthetic precursors as demonstrated by the synthesis of two cyclopentanes by Mg-induced dechlorination. The structure of trans-3,4-diphenylcyclopentanecarbonitrile was determined by single-crystal X-ray diffraction.

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Type
research article
DOI
10.1002/ejoc.201001213
Web of Science ID

WOS:000286964500006

Author(s)
Thommes, Katrin  
Fernandez-Zumel, Mariano Alfonso  
Buron, Charlotte
Godinat, Aurélien  
Scopelliti, Rosario  
Severin, Kay  
Date Issued

2011

Publisher

Wiley-Blackwell

Published in
European Journal of Organic Chemistry
Start page

249

End page

255

Subjects

Radical reactions

•

Ruthenium

•

Sequential reactions

•

Transfer Radical-Addition

•

Cyclization Atrc Reactions

•

Schiff-Base Ligands

•

Reducing Agent

•

Controlled Polymerization

•

Tert-Butyllithium

•

Copper-Complexes

•

Gamma-Lactams

•

Efficient

•

Reactivity

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCS  
Available on Infoscience
March 10, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/65244
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