406934-97-2

Upstream product

• 406934-87-0 2-[(2'S,5'R)-5'-benzyloxymethyltetrahydrofuran-2'-yl]ethan-1-ol 
• 406934-86-9 {(2S,5R)-5-[2-(tert-butyldimethylsilyloxy)ethyl]-tetrahydrofuran-2-yl}-methanol 
• 100-39-0 benzyl bromide 

Downstream Products

• 406934-88-1 (2R,5R)-2-benzyloxy-5-(5'-benzyloxypent-3'-ynyl)tetrahydrofuran 

Relevant academic research and scientific papers

Absolute stereochemistry of amphidinolide E

The absolute configurations at eight chiral centers in amphidinolide E (1), a cytotoxic 19-membered macrolide isolated from a marine dinoflagellate Amphidinium sp., were determined to be 2R, 7R, 8R, 13S, 16S, 17R, 18R, and 19R on the basis of detailed analysis of NMR data and by chemical means.