Lanthanide Trifluoromethanesulfonate-Catalyzed Asymmetric Aldol Reactions in Aqueous Media
Organic Letters2000Vol. 3(2), pp. 165–167
Citations Over TimeTop 10% of 2000 papers
Abstract
[figure: see text] Catalytic asymmetric aldol reactions catalyzed by lanthanide trifluoromethanesulfonates in aqueous media have been realized for the first time using a chiral crown ether.
Related Papers
- → Dynamic Measurements of Aqueous Lanthanide Triflate-Catalyzed Reactions Using Luminescence Decay(2009)35 cited
- → First Catalytic Aldol-Transfer Reaction via Aluminum Enolates: A New Way To Generate Aldol Adducts of Aldehydes from Aldol Adducts of Ketones(2000)30 cited
- → Solid State Structures, Solution Behavior, and Luminescence of Simple Tetrakis(2‐pyridylmethyl)ethylenediamine Lanthanide Complexes(2019)7 cited
- → Studies in Organocatalysts Synthesis for Direct Aldol Reaction(2013)
- → Homometallic Lanthanoids in Synthesis: Lanthanoid Triflate Catalyzed Synthetic Reactions(2005)