43139-78-2

Upstream product

• 66592-80-1 5-azido-5-deoxy-1,2-O-isopropylidene-β-L-idurono-3,6-lactone 
• 501-53-1 benzyl chloroformate 
• 14362-29-9 α-D-glucurono-γ-lactone 
• 103357-81-9 5-O-trifluoromethanesulfonyl-1,2-O-isopropylidene-α-D-glucofuranurono-6,3-lactone 
• 3067-56-9 isopropylidene glucuronolactone 
• 76542-57-9 Trifluoro-methanesulfonic acid (3aR,6S,7aR)-2,2-dimethyl-5-oxo-hexahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxol-6-yl ester 
• 3067-56-9 (3aR,6R,7aR)-6-Hydroxy-2,2-dimethyl-tetrahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxol-5-one 
• 76542-57-9 Trifluoro-methanesulfonic acid (3aR,6R,7aR)-2,2-dimethyl-5-oxo-hexahydro-furo[2',3':4,5]furo[2,3-d][1,3]dioxol-6-yl ester 
• 3067-56-9 D-glucurono-3,6-lactone acetonide 

Downstream Products

• 43139-79-3 ((3S,5S,6R)-5,6-Dihydroxy-2-oxo-hexahydro-furo[3,2-b]furan-3-yl)-carbamic acid benzyl ester 
• 111652-00-7 2S,4S,5S-2-(N-benzyloxycarbonyl)amino-6-O-tert-butyldimethylsilyl-5,6-dihydroxy-5-O-methanesulphonyl-hexan-4-olide 
• 108428-46-2 4S,5S-2-(N-benzyloxycarbonyl)amino-5,6-dihydroxy-6-O-methanesulphonyl-hex-2-en-4-olide 
• 108428-48-4 4S,5S-2-(N-benzyloxycarbonyl)amino-5,6-dihydroxy-6-O-tert-butyldimethylsilyl-hex-2-en-4-olide 
• 108428-49-5 2S,4S,5S-2-(N-benzyloxycarbonyl)amino-6-O-tert-butyldimethylsilyl-5,6-dihydroxy-hexan-4-olide 
• 111651-97-9 4S,5S,-2-(N-benzyloxycarbonyl)amino-5,6-dihydroxy-5,6-O-isopropylidene-hex-2-en-4-olide 
• 111651-99-1 2S,4S,5S-2-(N-benzyloxycarbonyl)amino-5,6-dihydroxy-5,6-O-isopropylidene-hexan-4-olide 
• 95863-87-9 (2S,4S,5R)-4-hydroxy-5-(hydroxymethyl)pyrrolidine-2-carboxylic acid 
• 43139-79-3 5-(N-benzyloxycarbonyl)amino-5-deoxy-L-iduronolactone 
• 108428-45-1 4S,5S-2-(N-benzyloxycarbonyl)amino-5,6-dihydroxyhex-2-en-4-olide 

Relevant academic research and scientific papers

THE SYNTHESIS OF POLYHYDROXYLATED AMINO ACIDS FROM GLUCURONOLACTONE: ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID AND 2R,3R,4R-DIHYDROXYPROLINE

The potential of D-glucuronolactone for the synthesis of polyhydroxylated amino acids is illustrated by the enantiospecific syntheses of 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid and 2R,3R,4R-dihydroxyproline.

ENANTIOSPECIFIC SYNTHESES OF 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2R,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID, 2S,4S,5S-DIHYDROXYPIPECOLIC ACID, AND BULGECININE FROM D-GLUCURONOLACTONE

The potential of D-glucuronolactone as a starting material for the synthesis of polyfunctional amino acids is illustrated by its conversion to 2S,3R,4R,5S-trihydroxypipecolic acid, 2R,3R,4R,5S-trihydroxypipecolic acid, 2S,4S,5S-dihydroxypipecolic acid, and bulgecinine.