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Solid-Phase Synthesis of Amine/Carboxyl...
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