647007-87-2

Upstream product

• 78-84-2 isobutyraldehyde 
• 212712-42-0 (+)-(S)-4′′-benzyl-3′′-(3-(3′,4′-methylenedioxyphenyl)propanoyl)oxazolidin-2′′-one 

Downstream Products

• 647008-08-0 (2S,3R)-3-hydroxy-5-(4-methoxyphenyl)-2-(3,4-methylenedioxybenzyl)-3-(1-methylethyl)-4-pentynoic acid 
• 647008-04-6 (2R,3R)-5-(4-methoxyphenyl)-2-(3,4-methylenedioxybenzyl)-3-(1-methylethyl)-4-pentyne-1,3-diol 
• 647008-05-7 (2R,3S)-5-(4-methoxyphenyl)-2-(3,4-methylenedioxybenzyl)-3-(1-methylethyl)-4-pentyne-1,3-diol 

Relevant academic research and scientific papers

Systematic strategy for the synthesis of cyanobacterin and its stereoisomers. 2. Asymmetric total synthesis of the 2- and 3-epimers of dechloro-cyanobacterin

Stereocontrolled total syntheses of the (2S,3R)- and (2R,3S)-isomers of the non-chlorinated analog of cyanobacterin, a potent photosynthesis inhibitor, were achieved. Since both the (2R,3R)- and (2S,3S)-isomers of this compound had been previously synthes