Please use this identifier to cite or link to this item:;2-7
Title: A selenide linker for "Traceless" solid-phase organic synthesis
Authors: Li, Z.
Kulkarni, B.A. 
Ganesant, A.
Keywords: Selenides
Solid-phase synthesis
Traceless linkers
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.;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
ISSN: 00063592
DOI: 10.1002/1097-0290(2000)71:23.0.CO;2-7
Appears in Collections:Staff Publications

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