Asymmetric Epoxidation of Chalcones Promoted by  Chiral Schiff Bases and Amino Alcohols

dc.contributor.author	Tianhua Shen
dc.contributor.author	Junqi Li
dc.contributor.author	Funa Cui
dc.contributor.author	Xiaocong Zhou
dc.contributor.author	Xiaoli Chen
dc.contributor.author	Qingbao Song
dc.date.accessioned	2023-10-24T07:16:43Z
dc.date.available	2023-10-24T07:16:43Z
dc.date.issued	2013-10-20
dc.identifier.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).	en_US
dc.identifier.issn	0253-5106
dc.identifier.uri	http://142.54.178.187:9060/xmlui/handle/123456789/19867
dc.description.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.).	en_US
dc.description.sponsorship	The chemical society of Pakistan is an approved society from the PSF.	en_US
dc.language.iso	en	en_US
dc.publisher	HEJ Research Institute of Chemistry, University of Karachi, Karachi.	en_US
dc.subject	Chiral ligands	en_US
dc.subject	L-phenylalanine	en_US
dc.subject	asymmetric epoxidation	en_US
dc.subject	enantioselective	en_US
dc.title	Asymmetric Epoxidation of Chalcones Promoted by Chiral Schiff Bases and Amino Alcohols	en_US
dc.type	Article	en_US