Journal article
Solid-Phase Synthesis of Amine/Carboxyl Substituted Prolines and Proline Homologues: Scope and Limitations
Abstract
A solid-phase procedure is used to synthesize racemic peptidomimetics based on the fundamental peptide unit. The peptidomimetics are constructed around proline or proline homologues variably substituted at the amine and carbonyl sites. The procedure expands the diversity of substituted peptidomimetic molecules available to the Distributed Drug Discovery (D3) project. Using a BAL-based solid-phase synthetic sequence the proline or proline …
Authors
Zhou Z; Scott WL; O’Donnell MJ
Journal
Molecules, Vol. 21, No. 3,
Publisher
MDPI
DOI
10.3390/molecules21030350
ISSN
1431-5157