3484-43-3Relevant articles and documents
Dimerization of butenolide structures. A biomimetic approach to the dimeric sesquiterpene lactones (±)-biatractylolide and (±)- biepiasterolide
Bagal, Sharanjeet K.,Adlington, Robert M.,Baldwin, Jack E.,Marquez, Rodolfo
, p. 9100 - 9108 (2007/10/03)
The biomimetic synthesis of the bisesquiterpene lactones (±)-biatractylolide 1 and (±)-biepiasterolide 2 via dimerization of the captodative stabilized radical 8 is reported. Atractylon 7 has also been shown to be a possible intermediate during the biosynthesis of biatractylolide 1, biepiasterolide 2, atractylolide 3, and hydroxyatractylolide 4.
TOTAL SYNTHESIS OF (+/-)-ATRACTYLON AND (+/-)-LINDESTRENE
Honan, Matthew C.
, p. 6393 - 6396 (2007/10/02)
The total synthesis of the eudesmane furanosesquiterpenes (+/-)-atractylon (1) and (+/-)-lindestrene (2) is described.Both 1 and 2 were synthesized via the methyl xanthate intermediate (10).