Publications by authors named "Mitsutoshi Maeda"
Org Biomol Chem
January 2020
Article Synopsis
- * The key intermediate for this synthesis, (-)-10-epi-axisonitrile-3, was created through a two-step process involving stereoselective cyclopropanation followed by a ring-opening reaction with the azide anion.
- * The final target exigurin was successfully constructed by applying a bioinspired Ugi reaction that combined (-)-10-epi-axisonitrile-3 with formaldehyde, sarcosine, and methanol, linking its terpene and amino acid components through an amide bond.
