Liquid phase parallel synthesis has been developed to synthesize a novel se
ries of iminodiacetic acid derivatives targeting the integrin receptors. Th
is library was synthesized using a four-step reaction sequence. In each ste
p of the sequence, the PEG-bound products were precipitated selectively and
the excess reagents and the by-products were removed by simple filtration,
The most notable result was that the library members were obtained in high
purities (>90% pure), (C) 1999 Elsevier Science Ltd. All rights reserved.