381719-00-2

Upstream product

• 693-25-4 n-pentylmagnesium bromide 
• 381718-99-6 (R)-5-O-Benzyl-4-O-tert-butyldimethylsilyl-4,5-dihydroxypentanal 
• 381718-98-5 Methyl (R)-5-O-benzyl-4-O-tert-butyldimethylsilyl-4,5-dihydroxypentanoate 
• 146582-86-7 (R)-5-Benzyloxy-4-hydroxy-pentanoic acid methyl ester 
• 98892-19-4 5-benzyloxy 4R-t-butyldimethylsiloxy 1-pentanol 
• 77697-15-5 (R)-(-)-γ-benzyloxymethyl-γ-butyrolactone 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 52813-63-5 (5R)-2,3,4,5-tetrahydro-5-hydroxymethyl-2-furanone 

Downstream Products

• 381719-05-7 (R)-1-O-Benzyl-2-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-5-ethylenedithio-1,2-decandiol 
• 381719-06-8 (R)-1-O-Benzyl-2-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5-ethylenedithio-1,2-decandiol 
• 381719-04-6 (R)-1-O-Benzyl-5-ethylenedithio-1,2-decandiol 

Relevant academic research and scientific papers

Novel chiral glycerol analogues building blocks. Application to the synthesis of bioactive glycoglycerolipid analogues

Monoacylglycosylglycerols show anti-tumor promoting effects: in order to study the role of the ester function we have prepared by simple methods (R)-1-O-benzyl-1,2-decandiol, (R)-3-O-benzyl-1-O-hexyl-sn-glycerol, and (R)-1-O-benzyl-5-oxo-1,2-decandiol; these optically active compounds are building blocks for the synthesis of monohexanoylglycosylglycerol isosters.