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  4. Palladium-catalyzed desulfinylative C–C allylation of Grignard reagents and enolates using allylsulfonyl chlorides and esters
 
research article

Palladium-catalyzed desulfinylative C–C allylation of Grignard reagents and enolates using allylsulfonyl chlorides and esters

Volla, Chandra M Rao
•
Dubbaka, Srinivas Reddy  
•
Vogel, Pierre  
2009
Tetrahedron

2-Methylprop-2-ene-, prop-2-ene-, 1-methylprop-2-ene-, and (E)-but-2-enesulfonyl chlorides have been used as electrophilic partners in desulfinylative palladium- catalyzed C–C coupling with Grignard reagents and sodium salts of dimethyl malonate and methyl acetoacetate. Neopentyl alk-2-ene sulfonates can also be used as electrophilic partners in desulfinylative allylic arylations and allylic alkylations. The regioselectivity of the allylic arylation and alkylation depends on the nature of the catalyst. With PdCl2(PhCN)2, (E)-crotyl derivatives are formed in high regioselectivity using either 1- methylprop-2-eneor (E)-but-2-enesulfonyl chloride.

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Type
research article
DOI
10.1016/j.tet.2008.11.007
Web of Science ID

WOS:000262797900010

Author(s)
Volla, Chandra M Rao
Dubbaka, Srinivas Reddy  
Vogel, Pierre  
Date Issued

2009

Published in
Tetrahedron
Volume

65

Issue

2

Start page

504

Subjects

Allylic alkylation

•

Allylic arylation

•

Homogenous catalysis

•

Regioselective allylation

•

Palladium complexes

•

Sulfonate esters

•

Sulfonyl chlorides

•

Grignard reagents

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
December 14, 2008
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/32666
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