Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels–Alder and Friedel–Crafts reactions†
Shuo Qiao,Junming Mo,Cody B. Wilcox
Organic & Biomolecular Chemistry Pub Date : 01/24/2017 00:00:00 , DOI:10.1039/C6OB02801B
Abstract

The design and synthesis of recyclable imidazolidinone catalysts using GAP chemistry/technique was described. Their applications in asymmetric Diels–Alder and Friedel–Crafts reactions with α,β-unsaturated aldehydes resulted in excellent yields and higher enantioselectivities than previous processes. As recyclable small molecular catalysts, phosphonylated imidazolidinones can be recovered and reused for up to three runs without costing significant decrease in catalytic activity.

Graphical abstract: Chiral GAP catalysts of phosphonylated imidazolidinones and their applications in asymmetric Diels–Alder and Friedel–Crafts reactions