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  4. Desymmetrization of Prochiral Cyclopentenes Enabled by Enantioselective Palladium-Catalyzed Oxidative Heck Reaction
 
research article

Desymmetrization of Prochiral Cyclopentenes Enabled by Enantioselective Palladium-Catalyzed Oxidative Heck Reaction

Chen, Guihua  
•
Cao, Jian  
•
Wang, Qian  
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2020
Organic Letters

In the presence of a catalytic amount of Pd(TFA)2 and a chiral Pyox ligand under oxygen atmosphere, oxidative Heck reaction between arylboronic acids and 4- substituted or 4,4-disubstituted cyclopent-1-enes afforded the chiral arylated products with concurrent creation of two stereocenters in good yields with excellent diastereo- and enantioselectivities.

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Type
research article
DOI
10.1021/acs.orglett.9b04357
Author(s)
Chen, Guihua  
Cao, Jian  
Wang, Qian  
Zhu, Jieping  
Date Issued

2020

Published in
Organic Letters
Volume

22

Issue

1

Start page

322

End page

325

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
January 24, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/164901
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