Conditions for the sequential reaction of carbon dioxide with an acetylenic amine and carbon monoxide in the presenceof a PdI2–KI catalyst in alcohols are examined. The stereochemistry of the two 5-alkoxycarbonyl.methylene-3,4,4-trialkyl-1,3-oxazolidin-2-one stereoisomers obtained is attributed to different pathways on the basis of experiments carried out onalkyl and benzyl esters of N-alkyldimethylpropynylcarbamic acid and carbon monoxide.

CARBON DIOXIDE EFFECT ON PALLADIUM-CATALYZED SEQUENTIAL REACTIONS WITH CARBON MONOXIDE, ACETYLENIC COMPOUNDS AND WATER

GABRIELE, Bartolo;VELTRI L.
2003-01-01

Abstract

Conditions for the sequential reaction of carbon dioxide with an acetylenic amine and carbon monoxide in the presenceof a PdI2–KI catalyst in alcohols are examined. The stereochemistry of the two 5-alkoxycarbonyl.methylene-3,4,4-trialkyl-1,3-oxazolidin-2-one stereoisomers obtained is attributed to different pathways on the basis of experiments carried out onalkyl and benzyl esters of N-alkyldimethylpropynylcarbamic acid and carbon monoxide.
2003
Carbonylation; Carbon dioxide; Oxazolidinones; Palladium
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11770/156742
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