Literature DB >> 17044109

Reusable catalysts for the asymmetric Diels-Alder reaction.

Guillaume Chollet1, Marie-George Guillerez, Emmanuelle Schulz.   

Abstract

A new method for recycling chiral bis(oxazoline)-copper complexes is described based on the formation of charge-transfer complexes, their subsequent precipitation, and reuse after addition of new substrates. The conditions to perform this procedure were optimized in the presence of three bis(oxazoline)-based ligands. When associated with copper salts, these ligands efficiently catalyzed the Diels-Alder reaction between cyclopentadiene and alpha,beta-unsaturated acyloxazolidinones. These catalysts were successfully recycled up to ten times while maintaining their high activities and enantioselectivities.

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Year:  2007        PMID: 17044109     DOI: 10.1002/chem.200601081

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Recyclable iron(ii) caffeine-derived ionic salt catalyst in the Diels-Alder reaction of cyclopentadiene and α,β-unsaturated N-acyl-oxazolidinones in dimethyl carbonate.

Authors:  Di Meng; Dazhi Li; Thierry Ollevier
Journal:  RSC Adv       Date:  2019-07-15       Impact factor: 4.036

  1 in total

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