作者:A.R. Lister、S.C. Moratti
DOI:10.1016/j.tet.2006.08.012
日期:2006.10
A series of poly(phenyl ketone) dendrons have been constructed using a convergent strategy. An aryl fluoro-substituent is deactivated towards nucleophilic substitution by protection of a para-ketone as an acetal. This allows coupling to an activated aryl fluoride. Subsequent deprotection of the acetyl group then activates the first fluoro-substituent and allows the next generation of the dendron to be added. The synthesis of higher generations is complicated by a scrambling reaction, which lowers the yields. (c) 2006 Elsevier Ltd. All rights reserved.