Issue 2, 2015

Convergent synthesis of degradable dendrons based on l-malic acid

Abstract

New degradable polyester dendrons based on the cellular tricarboxylic acid cycle component L-malic acid were synthesized up to the third generation by convergent synthesis. The dendron wedges could be introduced in a stepwise, highly regioselective fashion. HMBC-NMR revealed that the C1-carbonyl on malic acid was exclusively esterified, before the reaction of the second dendron wedge at C4 took place. Degradation studies on a first generation dendron analyzed by HPLC showed that hydrolytic degradation of the dendron most profoundly takes place at pH 4 and pH 9 with the highest degradation rate at alkaline pH. NMR shows that the dendron degrades to malic acid and fumaric acid derivatives. Preliminary studies performed in the cell culture show low toxicity of the dendrons in concentrations of up to 50 μg mL−1.

Graphical abstract: Convergent synthesis of degradable dendrons based on l-malic acid

Supplementary files

Article information

Article type
Paper
Submitted
10 Jul 2014
Accepted
20 Nov 2014
First published
21 Nov 2014

New J. Chem., 2015,39, 1161-1171

Author version available

Convergent synthesis of degradable dendrons based on L-malic acid

U. Meyhoff, U. Riber and U. Boas, New J. Chem., 2015, 39, 1161 DOI: 10.1039/C4NJ01156B

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