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Asymmetric cyclopropanation catalyzed by C2-symmetric bis-(ephedrine)-Cu(II) complexes

✍ Scribed by Jian Gao; Shun He Zhong


Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
77 KB
Volume
191
Category
Article
ISSN
1381-1169

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✦ Synopsis


The asymmetric cyclopropanation of styrene with alkyl diazoacetate was performed with a series of Cu(II) complexes of novel chiral ligands, which were derived from substitution of 1,3-dibromopropane, 1,2-dibromoethane, ␣,␣ -dibromo-m-xylene and 2,6-bis(bromomethyl)pyridine with 1R, 2S-(-)-ephedrine. These prepared catalysts shown to be highly active in the enantioselective cyclopropanation with ee higher than 89% under the optimal conditions.


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Asymmetric Cyclopropanation of Styrene C
✍ Zhengning Li; Guosheng Liu; Zhuo Zheng; Huilin Chen πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 121 KB

Asymmetric cyclopropanation of olefins was carried out with chiral copper-Schiff base complexes derived from copper acetate monohydrate, substituted salicylaldehydes and a chiral amino alcohol. Substituents on salicylaldehyde framework demonstrate a significant effect on the steroselectivities. Thos