Peptide aldehydes are of great interest as enzyme inhibitors and as startin
g materials for further chemistry. The solid phase synthesis of such entiti
es is presented through three different approaches: a Weinreb amide linker,
a phenyl ester linker, which both can be reduced with hydrides to yield th
e target molecules, and finally an unsaturated linker which produces the de
sired compounds by ozonolysis. (C) 1999 Elsevier Science B.V. All rights re
served.