83085-15-8

Upstream product

• 183889-09-0 methyl (R,R)-2,3-dihydroxy-2,3-O-isopropylidenepent-4-enoate 

Downstream Products

• 1442090-00-7 2-C-azidomethyl-2,3,5-tri-O-benzyl-1-tert-butyldimethylsilyl-4-Omethanesulfonyl-L-ribitol 
• 1442089-99-7 2-C-azidomethyl-2,3,5-tri-O-benzyl-1-O-tert-butyldimethylsilyl-Lribitol 
• 1442089-98-6 2-C-azidomethyl-2,3,5-tri-O-benzyl-L-ribitol 
• 1442089-97-5 2-C-azidomethyl-2,3,5-tri-O-benzyl-L-ribono-1,4-lactone 
• 1442089-95-3 2-C-azidomethyl-5-O-benzhydryl-2,3-O-isopropylidene-L-ribono-1,4-lactone 
• 1442089-93-1 5-O-benzhydryl-2-C-hydroxymethyl-2,3-O-isopropylidene-L-ribono-1,4-lactone 
• 1463870-08-7 C₂₃H₂₃F₃O₈S 
• 4099-88-1 2,3-O-isopropylidene-L-ribofuranose 
• 1202748-22-8 5-O-benzhydryl-2,3-O-isopropylidene-L-ribono-1,4-lactone 
• 84856-97-3 Toluene-4-sulfonic acid (3aS,4S,6aS)-2,2-dimethyl-6-oxo-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 

Relevant academic research and scientific papers

Stereoselective transformations leading to pentono -1, 4-lactones

The readily available 2, 3-O-isopropylidene-D-erythrose has been stereoselectively transformed into L-ribono and D/L lyxonolactone derivatives via dihydroxylation, iodolactonisation and epoxidation. Also D-ribono-1,4-lactone was converted into L-lyxono-1,