280745-40-6

Upstream product

• 280745-38-2 2,3:4,5-Di-O-isopropylidene-L-manno-hexodialdose 
• 280745-35-9 2,3:4,5-Di-O-isopropylidene-D-manno-hexodialdose 
• 676259-86-2 2,3:4,5-bis-O-[(2S,3S)-2,3-dimethoxybutane-2,3-diyl]-D-ido-hexodialdose 
• 676259-87-3 (2S,3S,4aR,7aR,9S,10S,11aS,11bS)-6-Benzhydryl-2,3,9,10-tetramethoxy-2,3,9,10-tetramethyl-decahydro-1,4,8,11-tetraoxa-6-aza-dibenzo[a,c]cycloheptene 
• 676259-79-3 2,3:4,5-bis-O-[(2R,3R)-2,3-dimethoxybutane-2,3-diyl]-L-ido-hexodialdose 
• 676259-80-6 (2R,3R,4aS,7aS,9R,10R,11aR,11bR)-6-Benzhydryl-2,3,9,10-tetramethoxy-2,3,9,10-tetramethyl-decahydro-1,4,8,11-tetraoxa-6-aza-dibenzo[a,c]cycloheptene 
• 280745-36-0 (3R,4R,5R,6R)-N-Benzhydryl-3,4:5,6-bis(isopropylidenedioxy)azepane 
• 280745-39-3 (3S,4S,5S,6S)-N-Benzhydryl-3,4:5,6-bis(isopropylidenedioxy)azepane 

Downstream Products

• 280745-41-7 1,6-dideoxy-1,6-imino-iditol 
• 16647-61-3 1,6-dideoxy-1,6-imino-(2S,3R,4R,5S)-L-iditol 
• 178964-40-4 1,6-dideoxy-1,6-imino-D-mannitol 
• 280745-41-7 (3S,4S,5S,6S)-3,4,5,6-Tetrahydroxyazepane 

Relevant academic research and scientific papers

Syntheses of tetrahydroxyazepanes from chiro-inositols and their evaluation as glycosidase inhibitors

Two pairs of C2-symmetric tetrahydroxyazepanes [(-), (+)-1 and (-), (+)-2] have been synthesized from the enantiomeric chiro-inositols and evaluated as glycosidase inhibitors. Alternative syntheses of ido-tetrahydroxyazepanes (-)- and (+)-2 fro

Short practical synthesis of (3R,4R,5R,6A)-tetrahydroxyazepane and (3S,4S,5S,6S)-trahydroxyazepane from D- And L-chiroinositol, respectively

The polyhydroxylated azepanes (3R,4R,5R,6R)-tetrahydroxyazepane (-)-l and (35,45,5S,65)-tetrahydroxyazepane (+)-1 are synthesised from D-and L-c/j/ro-inositol, respectively. Key transformations in the reaction sequence include a glycol-fission reaction wi