136289-13-9

Upstream product

• 2746-25-0 p-Methoxybenzyl bromide 
• 136289-12-8 (4S,5R,6R)-4-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-6-((S)-2-hydroxy-1-methoxy-ethyl)-2,2-dimethyl-[1,3]dioxan-5-ol 
• 136289-11-7 (4R,4aS,7R,7aR)-4-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-7-methoxy-2,2-dimethyl-tetrahydro-6H-furo[3,2-d][1,3]dioxin-6-one 
• 6605-22-7 3,5:6,7-bis-O-(1-methylethylidene)-α-D-glucoheptonic γ-lactone 

Downstream Products

• 136289-17-3 (R)-2,2-Dimethyl-4-[(1R,2R,3S,4S)-1,2,3-tris-benzyloxy-4-methoxy-5-(4-methoxy-benzyloxy)-pentyl]-[1,3]dioxolane 
• 136289-15-1 (1R,2R,3S,4S)-2-Benzyloxy-1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-methoxy-5-(4-methoxy-benzyloxy)-pentane-1,3-diol 
• 136289-16-2 (R)-1-{(4R,5S,6S)-5-Benzyloxy-6-[(S)-1-methoxy-2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxan-4-yl}-ethane-1,2-diol 
• 136289-14-0 (4R,5R,6S)-5-Benzyloxy-4-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-6-[(S)-1-methoxy-2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxane 

Relevant academic research and scientific papers

AN ENANTIOSPECIFIC APPROACH TOWARDS THE C10 SIDE-CHAIN OF BENGAMIDES

An enantiospecific approach to the highly hydroxylated C10 side-chain, common to all bengamides, starting from α-D-glucoheptonic γ-lactone, has been described.