479665-67-3

Upstream product

• 479665-65-1 N-(tert-butoxycarbonyl)-1,4,5-trideoxy-1,4-imino-2,3-O-isopropylidene-8-O-(p-methoxybenzoyl)-D-threo-L-lyxo-octitol 
• 479665-64-0 (E)-N-(tert-butoxycarbonyl)-2,3,4,5,8-pentadeoxy-5,8-imino-6,7-O-isopropylidene-1-O-(p-methoxybenzoyl)-L-arabino-oct-2-enitol 
• 479665-58-2 methyl (E)-N-(tert-butoxycarbonyl)-2,3,4,5,8-pentadeoxy-5,8-imino-6,7-O-isopropylidene-L-arabino-oct-2-enonate 
• 479665-74-2 (E)-N-(tert-butoxycarbonyl)-2,3,4,5,8-pentadeoxy-5,8-imino-6,7-O-isopropylidene-L-arabino-oct-2-enitol 
• 294172-61-5 3,6-[(tert-butoxy)carbonyl]imino-2,3,6-trideoxy-4,5-O-isopropylidene-L-arabino-hexose 

Relevant academic research and scientific papers

Stereoselective syntheses of 1,4-dideoxy-1,4-imino-octitols and novel tetrahydroxyindolizidines

A new route for the preparation of four new indolizidines, (1R,2S,6S,7S,8aS)- and (1R,2S,6R,7R,8aS)-1,2,6,7-tetrahydroxyindolizidine (30 and 32) and (1S,2R,7S,8S,8aR)- and (1S,2R,7R,8R,8aR)1,2,7,8-tetrahydroxyindolizidine (44 and 46), is reported. The syn

A convenient stereoselective route to novel tetrahydroxyindolizidines

A convenient stereoselective route, for the preparation of novel tetrahydroxyindolizidines, based on syn-hydroxylation reactions of alkenyl pyrrolidines followed by cyclization, is reported. Derivatives of (+)-swainsonine are prepared.