855517-38-3

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 261630-98-2 (1R,5R,8R)-8-Hydroxy-2-oxabicyclo[3.3.0]oct-6-en-3-one 
• 855517-37-2 (1R,5R,8R)-8-benzyloxy-2-oxabicyclo[3.3.0]oct-6-en-3-one 

Downstream Products

• 732308-58-6 (1S,2S,3S,4S,5R)-4-benzylamino-5-(hydroxymethyl)-1,2-isopropylidenecyclopentane-1,2,3-triol 
• 732308-42-8 (1S,2S,3S,4S,5R)-4-N-benzylamino-5-hydroxymethyl-cyclopentane-1,2,3-triol 
• 855517-53-2 (1R,2R,3S,4S,5R)-1-O-mesyl-2-O-(benzylcarbamoyl)-3,4-O-isopropylidene-5-(2-O-tert-butyldimethylsilyl-hydroxyethyl)-cyclopentane-1,2,3,4-tetrol 
• 855517-51-0 (1R,2R,3S,4S,5R)-1-O-mesyl-2-O-benzyl-3,4-O-isopropylidene-5-(2-O-tert-butyldimethylsilyl-hydroxyethyl)-cyclopentane-1,2,3,4-tetrol 
• 855517-54-3 (1S,2S,3S,4S,5S)-4-N-benzyl-6-(2-O-tert-butyldimethylsilyl-hydroxyethyl)-7,8-isopropylidenedioxy-2-oxa-4-azabicyclo[3.3.0]octan-3-one 
• 855517-46-3 (1R,2R,3S,4S,5R)-1-O-mesyl-2-O-(benzylcarbamoyl)-3,4-O-isopropylidene-5-acetoxymethyl-cyclopentane-1,2,3,4-tetrol 
• 855517-50-9 (1R,2S,3S,4S,5S)-2-O-benzyl-3,4-O-isopropylidene-5-(2-O-tert-butyldimethylsilyl-hydroxyethyl)-cyclopentane-1,2,3,4-tetrol 
• 855517-44-1 (1R,2R,3S,4S,5R)-1-O-mesyl-2-O-benzyl-3,4-O-isopropylidene-5-acetoxymethyl-cyclopentane-1,2,3,4-tetrol 
• 855517-42-9 (1R,2S,3S,4S,5S)-2-O-benzyl-3,4-O-isopropylidene-5-acetoxymethyl-1,2,3,4-cyclopentane-tetrol 
• 855517-47-4 (1S,2S,3S,4S,5S)-4-N-benzyl-5-acetoxymethyl-7,8-isopropylidenedioxy-2-oxa-4-azabicyclo[3.3.0]oct-3-one 
• 855517-55-4 (1S,2R,3S,4S,5S)-1,2-isopropylidene-4-benzylamino-5-(2-hydroxyethyl)-1,2,3-cyclopentanetriol 
• 855517-40-7 (1R,2S,3S,4S,5R)-1-formyloxy-2-benzyloxy-3,4-O-isopropylidene-5-iodomethyl-1,2,3,4-cyclopentane-tetrol 
• 855517-41-8 (1R,2S,3S,4S,5S)-2-O-benzyl-3,4-O-isopropylidene-5-iodomethyl-cyclopentane-1,2,3,4-tetrol 
• 855517-49-6 (1R,2S,3S,4S,5S)-2-O-benzyl-3,4-O-isopropylidene-5-(2-hydroxyethyl)-cyclopentane-1,2,3,4-tetrol 

Relevant academic research and scientific papers

Synthesis of aminocyclopentanols: α-D-galacto configured sugar mimics

Four aminocyclopentanols, as mimics of putative intermediates in the hydrolysis of α-D-galactosides, have been synthesized through a number of stereoselective transformations using the cis-fused cyclopentane-1,4-lactone (1R, 5S, 7R, 8R)-7,8-dihydroxy-2-ox