248582-07-2

Upstream product

• 248582-05-0 (+)-(2S)-1-{2-[(E)-pent-3-enyl]-1,3-dithian-2-yl}-4-(trityloxy)butan-2-ol 
• 248582-06-1 (+)-(2S)-4-{2-[(E)-pent-3-enyl]-1,3-dithian-2-yl}butane-1,3-diol 
• 241819-10-3 2-(pent-trans-3-enyl)-[1,3]-dithiane 
• 25166-87-4 trans-4-hexenal 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 86918-62-9 (3S,8E)-1,3-dihydroxydec-8-en-5-one 

Downstream Products

• 248582-10-7 (3R,5S,8E)-5-[(benzyloxy)amino]dec-8-ene-1,3-diol 
• 248582-09-4 (3R,5R,8E)-5-[(benzyloxy)amino]dec-8-ene-1,3-diol 

Relevant academic research and scientific papers

Synthesis of (+)-(S)-streptenol A and biomimetic synthesis of (2R,4S)- and (2S,4S)-2-(pent-3-enyl)piperidin-4-ol

(+)-(S)-Streptenol A is synthesized by coupling a 1,3-dithiane with an optically pure epoxide. The absolute configuration of (+)-(S)-streptenol A is thereby correlated with that of (S)-malic acid. Stereoselective reduction of an oxime that could easily be