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Updated: Feb 11, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks MOFs
Published on: January 17, 2020
Highly Enantioselective Copper-Phosphoramidite Catalyzed Kinetic Resolution of Chiral 2-Cyclohexenones
Robert Naasz1, Leggy A Arnold1, Adriaan J Minnaard1
1Department of Organic and Molecular Inorganic Chemistry Stratingh Institute, University of Groningen Nijenborgh 4, 9747 AG Groningen (The Netherlands) Fax: (+31) 50-363-4296.
Abstract:
A variety of substituted 2-cyclohexenones, such as (R)-1, is obtained enantiomerically pure by employing the chiral copper-phosphoramidite complex [Cu(OTf)2 L*] as a highly efficient catalyst for their kinetic resolution (>99 % ee at 52 % conversion, selectivity S>200). These important building blocks can be obtained on a synthetically interesting scale, as was demonstrated by the successful multigram resolution of 5-methyl-2-cyclohexenone. Tf=trifluoromethanesulfonyl.
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