Enantiopure fluorous 1,2-diaryl-1,2-diaminoethanes: synthesis and applications in asymmetric organometallic catalysis

Bayardon, J; Sinou, D

HERO ID

4936120

Reference Type

Journal Article

Year

2008

HERO ID 4936120
In Press No
Year 2008
Title Enantiopure fluorous 1,2-diaryl-1,2-diaminoethanes: synthesis and applications in asymmetric organometallic catalysis
Authors Bayardon, J; Sinou, D
Page Numbers 26-35
Abstract The synthesis of a new enantiopure fluorous 1,2-diaryl-1,2-diaminoethane bearing two fluorous ponytails is described. The palladium-catalyzed reaction of 1,3-diphenyl-2-propenyl acetate with dimethyl malonate in the presence of this ligand and its analogue bearing four fluorous ponytails gave the alkylated product with ee up to 44%. Their application as ligands in hydrogen transfer reactions associated with rhodium, iridium, or ruthenium in a two-phase system gave ee up to 39%, the catalyst being recycled without loss of enantioselectivity in the case of the ruthenium complex.
Wosid WOS:000260410200004
Is Certified Translation No
Dupe Override No
Comments Journal:ARKIVOC 1424-6376
Is Public Yes
Keyword Enantiopure fluorous diamines; asymmetric catalysis; allylic alkylation; hydrogen-transfer reaction