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|Title:||A selenide linker for "Traceless" solid-phase organic synthesis||Authors:||Li, Z.
|Issue Date:||2000||Citation:||Li, 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. https://doi.org/10.1002/1097-0290(2000)71:23.0.CO;2-7||Abstract:||4-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.||Source Title:||Biotechnology and Bioengineering||URI:||http://scholarbank.nus.edu.sg/handle/10635/111767||ISSN:||00063592||DOI:||10.1002/1097-0290(2000)71:23.0.CO;2-7|
|Appears in Collections:||Staff Publications|
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