Total synthesis of ascididemin via anionic cascade ring closure
Research output: Contribution to journal › Journal article › Research › peer-review
Ida Nymann Petersen, François Crestey, Jesper Langgaard Kristensen
A new and convergent synthesis of ascididemin is presented. Using an anionic cascade ring closure as the key step, this natural product is obtained in 45% overall yield in just 6 steps starting from 2'-fluoroacetophenone. This new approach was extended to the synthesis of a new isomer of ascididemin.
|Publication status||Published - 2012|