Starting from suitably protected amino acids, mercaptoimidazoles were synthesized either from the acid or including the amine nitrogen itself. A preliminary optimisation study led to efficient conditions for the obtention of the imidazole ring. These conditions are compatible with the presence of amino acid or dipeptide scaffolds.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/b810678a | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!