212056-64-9

Upstream product

• 212056-63-8 (R)-5-[(S)-1-(4-Methoxy-benzyloxymethoxy)-3-methyl-but-2-enyl]-5H-furan-2-one 

Downstream Products

• 212056-70-7 2,2-Dimethyl-propionic acid 3-[(2R,3R,4S,5S,6R)-5-(tert-butyl-dimethyl-silanyloxy)-6-hydroxymethyl-3-(4-methoxy-benzyloxymethoxy)-4-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-pyran-2-yl]-propyl ester 
• 212056-68-3 2,2-Dimethyl-propionic acid (4R,5R,6S,7S)-7-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-5-(4-methoxy-benzyloxymethoxy)-6-(2-trimethylsilanyl-ethoxymethoxy)-non-8-enyl ester 
• 212056-67-2 (R)-5-[(1R,2S,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-1-(4-methoxy-benzyloxymethoxy)-2-(2-trimethylsilanyl-ethoxymethoxy)-pent-4-enyl]-dihydro-furan-2-one 
• 212056-66-1 (R)-5-[(1S,2S,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-1-(4-methoxy-benzyloxymethoxy)-pent-4-enyl]-dihydro-furan-2-one 
• 212056-65-0 (R)-(4-Methoxy-benzyloxymethoxy)-((R)-5-oxo-tetrahydro-furan-2-yl)-acetaldehyde 

Relevant academic research and scientific papers

Synthesis of the C19 through C27 segment of okadaic acid using vinylogous urethane aldol chemistry: Part III

The synthesis of the C-19 through C-27 segment of the marine natural product okadaic acid was accomplished employing a highly enantio- and diasteroselective aldol coupling reaction of a chiral vinylogous urethane lactone enolate. The remainder of the carb