Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/60093
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorLi, CB-
dc.creatorCui, Y-
dc.creatorZhang, WQ-
dc.creatorLi, JL-
dc.creatorZhang, SM-
dc.creatorChoi, MCK-
dc.creatorChan, ASC-
dc.date.accessioned2016-11-21T02:35:58Z-
dc.date.available2016-11-21T02:35:58Z-
dc.identifier.issn1001-8417-
dc.identifier.urihttp://hdl.handle.net/10397/60093-
dc.language.isoenen_US
dc.publisherChinese Chemical Societyen_US
dc.rights© 2002 中国学术期刊电子杂志出版社。本内容的使用仅限于教育、科研之目的。en_US
dc.rights© 2002 China Academic Journal Electronic Publishing House. It is to be used strictly for educational and research purposes.en_US
dc.subjectOxime ethersen_US
dc.subjectSynthesis.en_US
dc.titleA convenient and efficient procedure for oxime ethersen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage95-
dc.identifier.epage96-
dc.identifier.volume13-
dc.identifier.issue2-
dcterms.abstractAcetophenone oxime and benzaldehyde oxime were converted to oxime ethers in the presence of alkyl halide or methyl sulfate and KOH in aqueous DMSO in 5 to 70 min. The yields of oxime ethers were 70 - 96%.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChinese chemical letters, 2002, v. 13, no. 2, p. 95-96-
dcterms.isPartOfChinese chemical letters-
dcterms.issued2002-
dc.identifier.rosgroupidr05785-
dc.description.ros2001-2002 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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