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https://doi.org/10.1021/ol403406y
DC Field | Value | |
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dc.title | Copper-catalyzed trifluoromethylselenolation of aryl and alkyl halides: The silver effect in transmetalation | |
dc.contributor.author | Chen, C. | |
dc.contributor.author | Hou, C. | |
dc.contributor.author | Wang, Y. | |
dc.contributor.author | Hor, T.S.A. | |
dc.contributor.author | Weng, Z. | |
dc.date.accessioned | 2014-10-16T08:23:54Z | |
dc.date.available | 2014-10-16T08:23:54Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Chen, 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.issn | 15237060 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/93399 | |
dc.description.abstract | A 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol403406y | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ol403406y | |
dc.description.sourcetitle | Organic Letters | |
dc.description.volume | 16 | |
dc.description.issue | 2 | |
dc.description.page | 524-527 | |
dc.description.coden | ORLEF | |
dc.identifier.isiut | 000330098400051 | |
Appears in Collections: | Staff Publications |
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