853785-06-5Relevant academic research and scientific papers
Chemoenzymatic total synthesis of the phytotoxic lactone herbarumin III
Nanda, Samik
, p. 3661 - 3663 (2007/10/03)
Asymmetric total synthesis of phytotoxic nonenolide herbarumin III was accomplished by a chemoenzymatic approach. The main highlight of the synthesis was to fix the hydroxyl stereocenters (C7 and C9) by lipase catalyzed irreversible transesterification.
Synthesis of a Novel Acetylenic Ester, Methyl (E)-5-Octadecen-7,9-diynoate
Mhaskar, S.Y.,Lakshminarayana, G.
, p. 2001 - 2009 (2007/10/02)
We, herein, report synthesis of methyl ester of (E)-5-octadecen-7,9-diynoic acid, one of the novel acetylenic fatty acids of Paramacrolobium caeruleum root bark with unique biological activity, by coupling synthesized C1 to C8 fragment with 1-decyne.
