Chiral Room Temperature Ionic Liquids as Enantioselective Promoters for the Asymmetric Aldol Reaction
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Other documents of the author: González, Laura; Escorihuela, Jorge; Altava, Belen; Burguete, M. Isabel; Luis, Santiago V.
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comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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http://dx.doi.org/10.1002/ejoc.201402436 |
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Title
Chiral Room Temperature Ionic Liquids as Enantioselective Promoters for the Asymmetric Aldol ReactionAuthor (s)
Date
2014Publisher
Wiley Online LibraryISSN
1434-193XType
info:eu-repo/semantics/articlePublisher version
http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201402436/abstractSubject
Abstract
Chiral ionic liquids derived from natural amino acids are shown to be green and efficient media for direct asymmetric aldol reactions at room temperature catalyzed by (S)-proline. The corresponding aldol products were ... [+]
Chiral ionic liquids derived from natural amino acids are shown to be green and efficient media for direct asymmetric aldol reactions at room temperature catalyzed by (S)-proline. The corresponding aldol products were obtained with moderate to good enantioselectivities. A transfer of chirality from the chiral reaction media has been observed as well as the participation of match/mismatch interactions of the chiral medium with both enantiomers of proline. Moreover, these catalytic systems were easily recovered by simple filtration, and studies on their reuse have demonstrated that recycling is possible for at least four runs with only a slight reduction in activity. [-]
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European Journal of Organic Chemistry, 2014, vol. 2014, nº 24Rights
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- QUIO_Articles [702]