Please use this identifier to cite or link to this item:
Title: Intermolecular conjugate addition of alkyl radicals on solid phase
Authors: Zhu, X.
Ganesan, A. 
Issue Date: 1999
Source: Zhu, X.,Ganesan, A. (1999). Intermolecular conjugate addition of alkyl radicals on solid phase. Journal of Combinatorial Chemistry 1 (2) : 157-162. ScholarBank@NUS Repository.
Abstract: The conjugate addition of alkyl radicals, generated photolytically from the corresponding Barton esters, to acrylate immobilized on solid-phase was investigated. Using cross-linked polystyrene, acrylic acid was loaded with either the Wang or Rink linkers, and the reactions were carried out with 10 equiv of Barton ester. The yields following resin cleavage by trifluoroacetic acid were comparable to Barton's solution-phase results. TentaGel resins gave approximately 15% poorer yields, possibly due to radical quenching by the poly(ethylene glycol) spacer. With the Barton ester from cyclopent-2-enylacetic acid, the initial product of conjugate addition is capable of further intramolecular cyclization followed by attack of a second acrylate chain, resulting in polymer cross-linking.
Source Title: Journal of Combinatorial Chemistry
ISSN: 15204766
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Page view(s)

checked on Feb 17, 2018

Google ScholarTM


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.