Synthetic approaches to a variety of substituted glycoluril compounds are presented herein. We have applied several of these compounds in the solution-phase synthesis of combinatorial libraries, and we have developed methods to differentiate individual reaction sites for the stepwise synthesis of individual polyfunctionalized compounds.
Synthesis of a model analog of the cyclic decadepsipeptide intercalating agent luzopeptin A (antibiotic BBM 928A) containing proline, valine, and unsubstituted quinoline substituents
[EN] PEPTIDE NUCLEIC ACID (PNA) MONOMERS WITH AN ORTHOGONALLY PROTECTED ESTER MOIETY<br/>[FR] MONOMÈRES D'ACIDE NUCLÉIQUE PEPTIDIQUE (ANP) AVEC UNE FRACTION ESTER À PROTECTION ORTHOGONALE