96530-38-0

Upstream product

• 96530-39-1 Methyl-2-O-p-toluolsulfonyl-3,4-di-O-acetyl-6-desoxy-6-iod-α-D-glucopyranosid 
• 54497-89-1 methyl 2,6-bis-α-D-glucopyranoside 

Downstream Products

• 96691-85-9 methyl 3,4-anhydro-6-deoxy-6-iodo-2-O-(p-tolylsulphonyl)-α-D-galactopyranoside 
• 96691-87-1 methyl 4-O-benzoyl-3-O-benzyl-6-deoxy-6-iodo-2-O-(p-tolylsulphonyl)-α-D-gulopyranoside 
• 96691-88-2 methyl 3,4-di-O-benzyl-6-deoxy-6-iodo-2-O-(p-tolylsulphonyl)-α-D-gulopyranoside 
• 96691-89-3 Toluene-4-sulfonic acid (E)-(S)-1-((1R,2S)-1,2-bis-benzyloxy-but-3-enyl)-4-oxo-pent-2-enyl ester 
• 96691-86-0 methyl 3-O-benzyl-6-deoxy-6-iodo-2-O-(p-tolylsulphonyl)-α-D-gulopyranoside 

Relevant academic research and scientific papers

Unsaturated Carbohydrates. Part 27. Synthesis of (-)-exo-Brevicomin from a Nona-3,8-dienulose Derivative

The (-)-enantiomer (11) of the insect pheromone (+)-exo-brevicomin has been synthesized directly by hydrogenation-hydrogenolysis of the L-lyxo-nona-3,8-dienulose derivative (10).Epoxide ring opening of the methyl 3,4-anhydro-D-galactopyranoside (6), which

The formation of branched-chain deoxypentofuranosides by ring contraction in the reductive desulfonyloxylation of hexopyranoside p-toluenesulfonates

Several methyl 6-deoxy-, 6-deoxy-6-halo-, and 6-O-p-tolylsulfonylhexopyranoside 2- and 4-p-toluenesulfonates reacted readily with lithium triethylborohydride in boiling tetrahydrofuran under reductive desulfonyloxylation at C-2 and C-4, respectively, and