Synfacts 2007(8): 0818-0818  
DOI: 10.1055/s-2007-968786
Synthesis of Materials and Unnatural Products
© Georg Thieme Verlag Stuttgart · New York

Efficient Synthesis of Dendrimers via A Chemoselective Approach

Contributor(s): Timothy M. Swager, Wei Zhang
P. Antoni, D. Nyström, C. J. Hawker, A. Hult, M. Malkoch*
Royal Institute of Technology, Stockholm, Sweden and University of California, Santa Babara, USA
Further Information

Publication History

Publication Date:
24 July 2007 (online)

Significance

The dendrimer derivatives of the Fréchet-type and 2,2-bis(methylol)propionic acid (bis-MPA) dendrimers were synthesized via an accelerated growth approach, which is based on the combination of click chemistry with traditional esterification/etherification reactions. The required monomer units for one-step generation growth are AB2-monomer (2) and CD2-monomer (4). The synthetic strategy allows the divergent preparation of a fourth-generation dendrimer (2nd generation dendrimer 5 is shown) in only four steps and in multi-gram quantities with an overall yield of 70% from the starting triphenol 1. The obtained dendritic block copolymer contains alternating layers of benzyl ether, triazole and benzyl ether groups. The orthogonality and efficiency of this strategy were demonstrated by monitoring each reaction with NMR and MALDI-TOF techniques.