192504-25-9Relevant academic research and scientific papers
Synthetic studies toward potent cytotoxic agent amphidinolide B: Synthesis of the entire Cl-C13 moiety of the bottom half
Chakraborty, Tushar K.,Suresh, Vayalakkada R.
, p. 565 - 566 (2007/10/03)
Sharpless asymmetric dihydroxylation and Nozaki-Hiyama-Kishi's Cr(II)-mediated coupling between an α-alkoxyaldehyde and a vinyl iodide are the key steps in the stereoselective synthesis of the entire C1-C13 segment of the bottom-half of amphidinolide B.
