64638-70-6

Upstream product

• 505-23-7 1,3 dithiane 
• 99050-14-3 3-O-Benzyl-5,6-didesoxy-1,2-O-isopropyliden-5-iod-3-C-methyl-β-L-talo-hexofuranose 
• 98003-98-6 3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-3-C-methyl-α-D-ribo-hex-5-enofuranose 
• 55533-86-3 3-O-Benzyl-3-C-methyl-1,2-O-isopropylidene-α-D-allofuranose 
• 98003-97-5 3-O-benzyl-1,2-O-isopropylidene-3-C-methyl-5,6-ditosyloxy-α-D-allofuranose 
• 99050-13-2 3-O-Benzyl-6-desoxy-1,2-O-isopropyliden-3-C-methyl-α-D-allo-hexofuranose 
• 99050-12-1 3-O-Benzyl-1,2-O-isopropyliden-3-C-methyl-6-O-(p-tolylsulfonyl)-α-D-allo-hexofuranose 

Downstream Products

• 102851-93-4 (2R,3R)-2-(benzyloxy)-3-hydroxy-2-methylpentanal 
• 120595-02-0 (2S,3R,4S,5R)-4-Benzyloxy-5-ethyl-4-methyl-tetrahydro-furan-2,3-diol 
• 64638-73-9 4,5-didesoxy-2-C-methyl-2-O-benzyl-3-O-formyl-D-erythro-al-pentose 
• 87641-44-9 (2S,3R,4S,5R)-1,3,4-trihydroxy-5-(4-methoxybenzyloxy)-2,4-dimethylheptane 
• 98003-93-1 (2S,3R,4S,5R)-1-benzoyloxy-3,4-dihydroxy-5-(4-methoxybenzyloxy)-2,4-dimethylheptane 
• 98004-01-4 (2E,4S,5R)-4-benzyloxy-1-hydroxy-2,4-dimethylhept-2-ene 
• 88040-12-4 (2S,3R,4R,5R)-2,3-epoxy-1-hydroxy-4,5-(4-methoxybenzylidenedioxy)-2,4-dimethylheptane 
• 98003-95-3 (2S,3R,4R,5R)-1-hydroxy-3,4-isopropylidene-5-(4-methoxybenzyloxy)-2,4-dimethylheptane 
• 98003-96-4 (2R,3R,4R,5R)-3,4-O-isopropylidene-5-(4-methoxybenzyloxy)-2,4-dimethylheptanal 
• 98049-35-5 (3R,4S,5R,6R,7R)-3-hydroxy-5,6-isopropylidenedioxy-7-(4-methoxybenzyloxy)-2,4,6-trimethylnon-1-ene 
• 98004-00-3 ethyl(2E,4S,5R)-4-benzyloxy-5-formyloxy-2,4-dimethylhept-2-enoate 
• 98102-67-1 (2E,4S,5R,6R,7R)-1-hydroxy-5,6-isopropylidenedioxy-7-(4-methoxybenzyloxy)-2,4,6-trimethylnon-2-ene 
• 98003-92-0 (2S,3R,4R,5R)-1,3-diacetoxy-4-hydroxy-5-(4-methoxybenzyloxy)-2,4-dimethylheptane 
• 98004-18-3 (2R,3R,4S,5R,6R,7R)-2,3-epoxy-1-hydroxy-5,6-isopropylidenedioxy-7-(4-methoxybenzyloxy)-2,4,6-trimethylnonane 

Relevant academic research and scientific papers

Chiral Building Units from Carbohydrates, XI. - 2-Lithio-1,3-dithiane-induced Reactions of 5,6-Dideoxy-5-iodohexofuranoses Leading to Open-chained Heptose Trimethylene Dithioacetals

The reaction of 5,6-dideoxy-5-iodohexofuranoses 5b, 7c, 8, 8a, and 20 with a large excess of 2-lithio-1,3-dithiane (1) yields the open-chained heptose trimethylene dithioacetals 21, 23, 24, 25, and 26.L-Configurated 5-iodides give Z-olefines, D-configurat

Chiral Synthesis of Polyketide-derived Natural Products. Part 4. Synthesis of a Left-hand Segment with Six Consecutive Chiral Centres of Dihydroerythronolide A for the Total Synthesis of Erythromycin A from D-Glucose

For the purpose of the total synthesis of erythromycin A (1) from D-glucose (2) with the aid of stereochemical control in acyclic systems and p-methoxyphenylmethyl (MPM) protection, (2R,3S,4S,5R,6R,7R)-1-hydroxy-5,6-isopropylidenedioxy-3,7-bis(4-methoxybe