1292297-89-2

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 726193-04-0 (S)-3-(1,4-dioxaspiro[4.5]decan-2-yl)propan-1-ol 
• 112980-46-8 ethyl (2'S)-3-(1',4'-dioxa-spiro[4.5]dec-2'-yl)-acrylate 
• 78008-36-3 (R)-2,3-cyclohexylideneglyceraldehyde 

Downstream Products

• 1026024-89-4 (S)-5-[(4-methoxybenzyl)oxy]pentane-1,2-diol 
• 1292297-90-5 (S)-2-{3-[(4-methoxybenzyl)oxy]propyl}oxirane 
• 1292297-91-6 (S)-7-(4-methoxybenzyloxy)hept-1-en-4-ol 
• 1292297-92-7 [(S)-7-(4-Methoxybenzyloxy)hept-1-en-4-yloxy](tert-butyl)dimethylsilane 
• 1292297-96-1 (S)-[(2R,3R)-3-(benzyloxy)pent-4-en-2-yl] 4-(tert-butyldimethylsilyloxy)hept-6-enoate 
• 1292297-97-2 (S)-[(2R,3R)-3-(benzyloxy)pent-4-en-2-yl] 4-hydroxyhept-6-enoate 
• 1292297-98-3 (Z,5S,9R,10R)-9-(benzyloxy)-3,4,5,6,9,10-hexahydro-5-hydroxy-10-methyloxecin-2-one 

Relevant academic research and scientific papers

Stereoselective Synthesis of Stagonolide G from d -Mannitol

A highly convergent, stereoselective total synthesis of a ten-membered lactone, stagonolide G, is described. Epoxide ring-opening with vinyl Grignard, Yamaguchi esterification and ring-closing metathesis are the key steps involved in the present approach.