90641-17-1Relevant academic research and scientific papers
Total synthesis of (±)-asteltoxin
Schreiber,Satake
, p. 4186 - 4188 (2007/12/18)
A convergent synthesis of (±)-asteltoxin has been achieved in 16 steps (3.0% overall yield) from 3,4-dimethylfuran. The attachment of the triene pyrone side chain to the bis(tetrahydrofuran) skeleton proceeds by way of the addition of the Corey equivalent to anion 3 to the aldehyde 2 and a subsequent aldol condensation-dehydration reaction of pyrone 4.
