Journal
CHEMICAL COMMUNICATIONS
Volume 46, Issue 2, Pages 222-224Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b917435d
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A highly diastereoselective addition of various Grignard reagents to chiral gamma-chlorinated N-tert-butanesulfinyl imine resulting in the formation of 2-substituted pyrrolidines is reported. This method is general and also efficient for the preparation of both enantiomers of 2-aryl, 2-alkyl and 2-vinyl substituted pyrrolidines in high yields.
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