Myxovirescin analogues via macrocyclic ring–closing metathesis

Myxovirescin analogues via macrocyclic ring–closing metathesis Synthesis of a tricyclic hexapeptide –via two consecutive ruthenium-catalyzed macrocyclization steps– with a constrained topology to mimic vancomycin's binding properties toward D-Ala-D-Ala dipeptide 6-Hydroxy to 6‴-amino tethered ring-to-ring macrocyclic aminoglycosides as probes for APH(3′)-IIIa kinase A novel approach to FR-900482 via ring forming metathesis Binaphthyl scaffolded peptoids via ring-closing metathesis reactions and their anti-bacterial activities Structure of myxovirescin A, a new macrocylic antibiotic from gliding bacteria The myxovirescins, a family of antibiotics from Myxococcus virescens (Myxobacterales). Design and synthesis via click chemistry of 8,9-anhydroerythromycin A 6,9-hemiketal analogues with anti-MRSA and -VRE activity Synthesis and biological evaluation of optically active conjugated γ- and δ-lactone derivatives Design and synthesis of peptide-based macrocyclic cyclophilin inhibitors