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Please use this identifier to cite or link to this item: https://doi.org/10.1002/1097-0290(2000)71:23.0.CO;2-7
DC FieldValue
dc.titleA selenide linker for "Traceless" solid-phase organic synthesis
dc.contributor.authorLi, Z.
dc.contributor.authorKulkarni, B.A.
dc.contributor.authorGanesant, A.
dc.date.accessioned2014-11-28T02:49:28Z
dc.date.available2014-11-28T02:49:28Z
dc.date.issued2000
dc.identifier.citationLi, Z.,Kulkarni, B.A.,Ganesant, A. (2000). A selenide linker for "Traceless" solid-phase organic synthesis. Biotechnology and Bioengineering 71 (2) : 104-106. ScholarBank@NUS Repository. <a href="https://doi.org/10.1002/1097-0290(2000)71:23.0.CO;2-7" target="_blank">https://doi.org/10.1002/1097-0290(2000)71:23.0.CO;2-7</a>
dc.identifier.issn00063592
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/111767
dc.description.abstract4-Bromophenethyl alcohol was protected as the THP ether, followed by reaction with magnesium and selenium to give the corresponding diselenide. Ether deprotection provides a diselenide diol, which is attached to solid-phase resins. The polymer-bound selenide anion is then generated, and functions as a traceless linker for electrophiles such as alkyl halides. © 2001 John Wiley & Sons, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/1097-0290(2000)71:23.0.CO;2-7
dc.sourceScopus
dc.subjectSelenides
dc.subjectSolid-phase synthesis
dc.subjectTraceless linkers
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.doi10.1002/1097-0290(2000)71:23.0.CO;2-7
dc.description.sourcetitleBiotechnology and Bioengineering
dc.description.volume71
dc.description.issue2
dc.description.page104-106
dc.description.codenBIBIA
dc.identifier.isiutNOT_IN_WOS
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