Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol403406y
DC FieldValue
dc.titleCopper-catalyzed trifluoromethylselenolation of aryl and alkyl halides: The silver effect in transmetalation
dc.contributor.authorChen, C.
dc.contributor.authorHou, C.
dc.contributor.authorWang, Y.
dc.contributor.authorHor, T.S.A.
dc.contributor.authorWeng, Z.
dc.date.accessioned2014-10-16T08:23:54Z
dc.date.available2014-10-16T08:23:54Z
dc.date.issued2014
dc.identifier.citationChen, C., Hou, C., Wang, Y., Hor, T.S.A., Weng, Z. (2014). Copper-catalyzed trifluoromethylselenolation of aryl and alkyl halides: The silver effect in transmetalation. Organic Letters 16 (2) : 524-527. ScholarBank@NUS Repository. https://doi.org/10.1021/ol403406y
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93399
dc.description.abstractA catalytic trifluoromethylselenolation of aryl and alkyl halides by a Cu(I) catalyst has been developed. A key intermediate, [(phen)Cu(SeCF3)]2 (5) was successfully isolated and characterized by X-ray diffraction. The important role of silver in the transmetalation process during the catalytic cycle was elucidated. A wide range of trifluoromethylselanes have been prepared from readily available starting materials from a method that tolerates various important functional groups. © 2013 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol403406y
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol403406y
dc.description.sourcetitleOrganic Letters
dc.description.volume16
dc.description.issue2
dc.description.page524-527
dc.description.codenORLEF
dc.identifier.isiut000330098400051
Appears in Collections:Staff Publications

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