Ontology highlight
ABSTRACT:
SUBMITTER: Wrobel M
PROVIDER: S-EPMC3458720 | biostudies-literature | 2012
REPOSITORIES: biostudies-literature
Beilstein journal of organic chemistry 20120706
A series of substituted diaryltriazoles was prepared by a solid-phase-synthesis protocol using a modified Wang resin. The copper(I)- or ruthenium(II)-catalyzed 1,3-cycloaddition on the polymer bead allowed a rapid synthesis of the target compounds in a parallel fashion with in many cases good to excellent yields. Substituted diaryltriazoles resemble a molecular structure similar to established terphenyl-alpha-helix peptide mimics and have therefore the potential to act as selective inhibitors fo ...[more]