Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/19867
Title: Asymmetric Epoxidation of Chalcones Promoted by Chiral Schiff Bases and Amino Alcohols
Authors: Tianhua Shen
Junqi Li
Funa Cui
Xiaocong Zhou
Xiaoli Chen
Qingbao Song
Keywords: Chiral ligands
L-phenylalanine
asymmetric epoxidation
enantioselective
Issue Date: 20-Oct-2013
Publisher: HEJ Research Institute of Chemistry, University of Karachi, Karachi.
Citation: Shen, T., Li, J., Cui, F., Zhou, X., Chen, X., & Song, Q. (2013). Asymmetric epoxidation of chalcones promoted by chiral schiff bases and amino alcohols. Journal of the Chemical Society of Pakistan, 35(5).
Abstract: A series of chiral ligands were conveniently prepared from L-phenylalanine and characterized. Their application to the asymmetric epoxidation of chalcone was studied. The results demonstrated that 3a were efficient catalysts for enantioselective epoxidation of chalcone in moderate yield (up to 58.6%) and high enantioselectivities (up to 90% e.e.).
URI: http://142.54.178.187:9060/xmlui/handle/123456789/19867
ISSN: 0253-5106
Appears in Collections:Issue 05

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