Progress toward the Total Synthesis of Bielschowskysin: A Stereoselective [2 + 2] Photocycloaddition
摘要:
The tetracyclic core of the diterpene bielschowskysin has been prepared as a single enantiomer via a stereoselective intramolecular [2 + 2] photocycloaddition of 5-alkylidene-2(5H)-furanone 3.
Progress toward the Total Synthesis of Bielschowskysin: A Stereoselective [2 + 2] Photocycloaddition
摘要:
The tetracyclic core of the diterpene bielschowskysin has been prepared as a single enantiomer via a stereoselective intramolecular [2 + 2] photocycloaddition of 5-alkylidene-2(5H)-furanone 3.