944943-16-2

Upstream product

• 944943-14-0 (1S,2R)-2-[benzyl(mesitylenyl)sulfonylamino]-1-phenylpropyl (2S,3S,5R,6S,8S)-3-hydroxy-9-(4-methoxyphenoxy)-2,5,8-trimethyl-5,6-bis[(triethylsilyl)oxy]nonanoate 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 187324-67-0 (1S,2R)-2-(N-benzyl-N-mesitylenesulfonyl)amino-1-phenyl-1-propyl propionate 
• 944943-12-8 (3R,4S,6S)-7-(4-methoxyphenoxy)-3,6-dimethyl-3,4-bis[(triethylsilyl)oxy]heptaldehyde 
• 944942-96-5 (3R,4S,6S)-7-(4-methoxyphenoxy)-3,6-dimethyl-3,4-bis[(triethylsilyl)oxy]heptan-1-ol 

Downstream Products

• 944943-18-4 (2R,3S,5R,6S,8S)-3-(tert-butyldimethylsilyloxy)-9-(4-methoxyphenoxy)-2,5,8-trimethyl-5,6-bis[(triethylsilyl)oxy]nonan-1-ol 
• 944943-20-8 (2S,3S,5R,6S,8S)-3-(tert-butyldimethylsilyloxy)-9-(4-methoxyphenoxy)-2,5,8-trimethyl-5,6-bis[(triethylsilyl)oxy]nonanal 
• 944943-22-0 (3R,4S,6R,7S,9S)-4-(tert-butyldimethylsilyloxy)-10-(4-methoxyphenoxy)-3,6,9-trimethyl-6,7-bis[(triethylsilyl)oxy]dec-1-ene 

Relevant academic research and scientific papers

Total synthesis of amphidinolide y by formation of trisubstituted (E)-double bond via ring-closing metathesis of densely functionalized alkenes

Amphidinolide Y, a 17-membered cytotoxic macrolide isolated from marine dinoflagellates, has been synthesized via ring-closing metathesis to assemble the congested trisubstituted (E)-double bond. The seco precursor was prepared from readily available chir