A concise synthetic entry to the C15-C38 fragment of okadaic acid by exploiting a Suzuki-Miyaura reaction for the rapid assembly of the spiroacetal substructures has been developed. The present synthesis was completed in 19 linear steps from a commercially available material, showcasing the efficiency of our synthetic strategy.
|Number of pages||4|
|Publication status||Published - 2015 Jan 16|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Organic Chemistry