537007-20-8Relevant academic research and scientific papers
Absolute stereochemistry of amphidinolide C: Synthesis of C-1-C-10 and C-17-C-29 segments
Kubota, Takaaki,Tsuda, Masashi,Kobayashi, Jun'ichi
, p. 1613 - 1625 (2003)
Two of each diastereomers of the C-1-C-10 and C-17-C-29 segments of amphidinolide C (1) were synthesized. Comparing the 1H NMR chemical shifts of its MTPA esters with those of linear methyl ester of 1, the absolute configurations at C-7, C-8, C-20, C-23, and C-24 in amphidinolide C (1) were confirmed to be all R.
