1274699-53-4

Upstream product

• 102308-32-7 (4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 1274699-54-5 C₂₇H₄₃NO₅Si 

Downstream Products

• 355138-93-1 (2S,3S,4R,5S)-3,4,5-trihydroxy-2-(hydroxymethyl)piperidin-1-ium chloride 
• 1274699-61-4 (S)-tert-butyl 4-((1S,2R,3S)-1-(benzyloxy)-2,3-dihydroxy-4-(tosyloxy)butyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 1274699-63-6 C₂₀H₂₇NO₇S 
• 1274699-62-5 (3S,4R,5S,6S)-5-(benzyloxy)-6-(hydroxymethyl)piperidine-3,4-diol 
• 1274699-65-8 (S)-tert-butyl 4-((R,E)-1-(benzyloxy)-4-chlorobut-2-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate 
• 1274699-57-8 (S)-tert-butyl 4-((R,E)-1-(benzyloxy)-4-hydroxybut-2-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate 
• 1011247-64-5 (S)-tert-butyl 4-((R,Z)-1-(benzyloxy)-4-hydroxybut-2-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate 

Relevant academic research and scientific papers

Scalable synthesis of (-)-trans-3-hydroxypipecolic acid via a useful chiral building block

A scalable synthesis of (-)-trans-2-(hydroxymethyl)-1,2,3,6- tetrahydropyridin-3-ol, a versatile chiral building block is described along with its transformation to (-)-trans-3-hydroxypipecolic acid.

Rapid and practical synthesis of (-)-1-deoxyaltronojirimycin

Herein a practical and scalable route to 1-deoxyaltronojirimycin is presented. The target is achieved in 9 steps and 43% yield featuring only two chromatographic purifications.