Publication | Closed Access
Macrolide Analogues of the Novel Immunosuppressant Sanglifehrin: New Application of the Ring-Closing Metathesis Reaction
47
Citations
0
References
1999
Year
Combinatorial ChemistryMacrocyclic CoreOrganic ChemistryHeterocycle ChemistryChemical BiologyImmunotherapyPharmaceutical ChemistryMedicinal ChemistryNovel Immunosuppressant SanglifehrinSanglifehrin ABiochemistryMechanism Of ActionPharmacologyBiomolecular EngineeringAnti-inflammatoryMacrolide AnaloguesHeterocyclicNatural SciencesRing-closing Metathesis ReactionConjugated 1,3-Diene MoietyMedicineSynthetic ChemistryDrug Discovery
Macrocycles containing a conjugated 1,3-diene moiety have been synthesized for the first time in good yields by the ring-closing metathesis reaction [Eq. (1)]. The new compounds represent cyclophilin-binding, simplified analogues of the macrocyclic core of sanglifehrin A, an immunosuppressant which binds with high affinity to cyclophilin.