935761-74-3

Upstream product

• 935761-70-9 (4S,5R,6E)-4,5-dihydroxy-7-methyl-6-decenenitrile 
• 5707-04-0 Phenylselenyl chloride 
• 935761-60-7 5-(4-benzyl-2-oxo-oxazolidin-3-yl)-4-(tert-butyl-dimethyl-silanyloxy)-5-oxo-pentanenitrile 
• 935761-69-6 4-(tert-butyl-dimethyl-silanyloxy)-5-hydroxy-7-methyl-dec-6-enenitrile 
• 935761-67-4 4-(tert-butyl-dimethyl-silanyloxy)-5-hydroxy-7-methyl-dec-6-enenitrile 
• 935761-61-8 4-(tert-butyl-dimethyl-silanyloxy)-5-oxo-pentanenitrile 

Relevant academic research and scientific papers

Toward a total synthesis of amphidinolide X and Y. The tetrahydrofuran- containing fragment C12-C21

(Chemical Equation Presented) The key THF derivative (9a) for an enantioseiective synthesis of amphidinolide X/Y was obtained from 1a via a selenoetherification reaction. In fact, among the cyclization methods investigated, the highest yield and stereocon