Homochiral primary amines, amino alcohols and alpha -amino esters have been reacted with 2-propynyl-1,3-dicarbonyl compounds under gold catalysis leading to 1,2,5-trisubstituted 3-acylpyrrole derivatives in moderate to high yields and high enantiomeric excess.

Conversion of Homochiral Amines and alpha-Amino esters to their Chiral 1,2,3,5-Substituted Pyrrole Derivatives via Gold-Catalyzed Amination/Annulation Reactions Of 2-Propynyl-1,3-Dicarbonyl Compounds

ARCADI, Antonio;
2001-01-01

Abstract

Homochiral primary amines, amino alcohols and alpha -amino esters have been reacted with 2-propynyl-1,3-dicarbonyl compounds under gold catalysis leading to 1,2,5-trisubstituted 3-acylpyrrole derivatives in moderate to high yields and high enantiomeric excess.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/1433
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