291297-64-8

Upstream product

• 78184-40-4 1-O-allyl-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 265312-91-2 1-O-allyl-2,3,4-tri-O-benzyl-6-O-(4-tolylsulfonyl)-α-D-glucopyranoside 
• 291297-62-6 Toluene-4-sulfonic acid (2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-hydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 545-06-2 trichloroacetonitrile 
• 291297-63-7 Thioacetic acid S-((2S,3S,4S,5R,6S)-3,4,5-tris-benzyloxy-6-hydroxy-tetrahydro-pyran-2-ylmethyl) ester 

Relevant academic research and scientific papers

Structural determination of sulfoquinovosyldiacylglycerol by chiral syntheses

Chiral sulfoquinovosyldiacylglycerols (SQDGs) have been synthesized to determine the absolute stereochemistry and the biological activities. The 1 H NMR spectrum of a natural SQDG is comparable to that of synthetic (2S)-SQDG rather than that of the (2R) analogue. The biological activity of the respective isomers for DNA polymerase α and β inhibition was not distinguishable in the enzymatic assay.