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Chiral imidazolidinones-catalyzed asymmetric reactions

  • Chengfu Yao*
  • , Caixia Sun
  • , Shaoyu Yan
  • , Haihong Wu
  • *Corresponding author for this work
  • East China Normal University

Research output: Contribution to journalArticlepeer-review

Abstract

Enantioselective organocatalytic processes have developed maturely in recent years with an impressive number of applications now available. Aminocatalysis has proven to be a powerful procedure for the enantioselective transformations owing to their potential advantages over metal-catalyzed processes; usually more stable, less expensive, readily available, no risk of metal leakage into environment or the product, and can be applied in less demanding reaction conditions. Chiral imidazolidinones is an important sort of aminocatalysts. The paper summarizes the applications and advances of chiral imidazolidinones in asymmetric catalytic reactions, such as Diels-Alder reaction, 1, 3-dipolar cycloaddition, Michael reaction, Friedel-Crafts alkylation. Moreover, the future applications of chiral imidazolidinones in the industry manufactures are also prospected.

Original languageEnglish
Pages (from-to)887-898
Number of pages12
JournalProgress in Chemistry
Volume20
Issue number6
StatePublished - Jun 2008

Keywords

  • Asymmetric reactions
  • Chiral imidazolidinones
  • Enamine
  • Iminium ions
  • Intermediate
  • Organocatalysis

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