138481-57-9

Upstream product

• 108-05-4 vinyl acetate 
• 2405-69-8 (2S*,3S*,4R*)-2,3,4-[tris(benzyloxy)]pentane-1,5-diol 
• 2405-69-8 2,3,4-tri-O-benzyl-D-arabinitol 

Downstream Products

• 138481-63-7 2,3,4-Tri-O-benzyl-5-O-acetyl-L-ribose 
• 138481-64-8 Acetic acid (2R,3S,4S)-2,3,4-tris-benzyloxy-5-oxo-pentyl ester 
• 96236-35-0 2,3,4-tri-O-benzyl-D-lyxose diethyl dithioacetal 
• 138481-58-0 (2S,3S,4S)-2,3,4-Tris-benzyloxy-5,5-bis-ethylsulfanyl-pentan-1-ol 
• 138924-89-7 (2S,3S,4R,5R)-1-Carbobenzoxy-3,4,5-tris(benzyloxy)-2-<(1R)-1-<(methoxymethyl)oxy>prop-2-enyl>piperidine 
• 138924-88-6 (2R,3R,4S,5R,6R)-5-Hydroxy-6-<(methoxymethyl)oxy>-1-N-phthalyl-2,3,4-tris(benzyloxy)oct-7-enamine 
• 138924-90-0 (2S,3S,4R,5R)-1-Carbobenzoxy-3,4,5-tris(benzyloxy)-2-<(1R)-3-hydroxy-1-<(methoxymethyl)oxy>propyl>piperidine 
• 138924-87-5 5-N-Phthalyl-2,3,4-tri-O-benzyl-D-ribose 
• 138924-93-3 5-N-Phthalyl-2,3,4-tri-O-benzyl-L-ribose 
• 138924-98-8 (2R,3R,4S,5R,6R)-5-Hydroxy-6-<(methoxymethyl)oxy>-1-N-phthalyl-2,3,4-tris(benzyloxy)oct-7-enamine mesylate 
• 138925-00-5 (2S,3R,4R)-2,3,4-Tri-O-benzyl-5-N-phthalyladonitol 
• 138925-02-7 (2S,3R,4R)-1-Phthalimido-2,3,4-tris(benzyloxy)-hex-5-ene 
• 139014-28-1 3,4,5-tri-O-benzyl-1,2-dideoxy-L-ribo-hex-1-enitol 
• 138924-99-9 (2S,3R,4R)-1-O-Acetyl-5-N-phthalyl-2,3,4-tri-O-benzyladonitol 

Relevant academic research and scientific papers

A Route to Several Stereoisomers of Castanospermine

The following three stereoisomers of castanospermine have been prepared: (1R,6R,7R,8S,8aR)-1,6,7,8-tetrahydroxyindolizidine (1), (1R,6S,7S,8S,8aR)-1,6,7,8-tetrahydroxyindolizidine (2), and (1R,6R,7S,8S,8aR)-1,6,7,8-tetrahydroxyindolizidine (3).Each of the

Biocatalytic Desymmetrizations of Pentitol Derivatives

Several acylations of pentitol derivatives mediated by Candida cylindracea have been shown to be enantio-, or diastereo-, group selective; a pattern emerges from the selectivities of these reactions which may have some predictive value.Key words: acylation; catalysis; Candida cylindracea lipase; kinetic amplification of diastereomeric excess