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Highly enantioselective aldol reactions catalyzed by a recyclable fluorous (S) pyrrolidine sulfonamide on water.

Organic letters (2008-02-15)
Liansuo Zu, Hexin Xie, Hao Li, Jian Wang, Wei Wang
RESUMEN

Fluorous (S) pyrrolidine sulfonamide serves as an efficient promoter for highly enantioselective aldol reactions of ketones and aldehydes with aromatic aldehydes on water. A notable feature of the organocatalyst is that it can be recovered from the reaction mixtures by simple fluorous solid-phase extraction and subsequently reused (up to seven cycles) without a significant loss of catalytic activity and stereoselectivity.

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Sigma-Aldrich
1,1,1-Trifluoro-N-[(2S)-2-pyrrolidinylmethyl]-methanesulfonamide, ≥98.5% (T)