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  2. MoST Organizations
  3. Pakistan Science Foundation
  4. Pakistan Science Foundation
  5. PSF Research Support (Scientific Research Journals)
  6. Journal of the Chemical Society of Pakistan
  7. Volume 35
  8. Issue 05
Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/19867
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dc.contributor.authorTianhua Shen-
dc.contributor.authorJunqi Li-
dc.contributor.authorFuna Cui-
dc.contributor.authorXiaocong Zhou-
dc.contributor.authorXiaoli Chen-
dc.contributor.authorQingbao Song-
dc.date.accessioned2023-10-24T07:16:43Z-
dc.date.available2023-10-24T07:16:43Z-
dc.date.issued2013-10-20-
dc.identifier.citationShen, 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.issn0253-5106-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/19867-
dc.description.abstractA 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.sponsorshipThe chemical society of Pakistan is an approved society from the PSF.en_US
dc.language.isoenen_US
dc.publisherHEJ Research Institute of Chemistry, University of Karachi, Karachi.en_US
dc.subjectChiral ligandsen_US
dc.subjectL-phenylalanineen_US
dc.subjectasymmetric epoxidationen_US
dc.subjectenantioselectiveen_US
dc.titleAsymmetric Epoxidation of Chalcones Promoted by Chiral Schiff Bases and Amino Alcoholsen_US
dc.typeArticleen_US
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