373647-01-9

Upstream product

• 3315-16-0 silver cyanate 
• 6192-00-3 (2E)-3-methoxy-2-propenoyl chloride 
• 373646-99-2 (2R,3R,4R)-4-amino-2-[(benzoyloxy)methyl]-3-(benzyloxy)tetrahydrofuran 
• 373646-95-8 (2R,3S,4S)-2-[(benzoyloxy)methyl]-3-(benzyloxy)-4-(p-toluenesulfonyloxy)tetrahydrofuran 
• 373646-97-0 (2R,3R,4R)-4-azido-2-[(benzoyloxy)methyl]-3-(benzyloxy)tetrahydrofuran 
• 373646-92-5 (3S,4R,5R)-5-[(benzoyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-ol 
• 373646-91-4 (3R,4R,5R)-5-[(benzyloxy)methyl]-4-(benzyloxy)tetrahydrofuran-3-ol 
• 373646-85-6 (2S,3S,4R)-3-benzyloxy-4-((1R/S)-(1-ethoxy)-ethoxy)-2-(iodomethyl)tetrahydrofuran 
• 373646-89-0 (3R,4R,5R)-4-(benzyloxy)-5-(hydroxymethyl)tetrahydrofuranol 
• 334784-71-3 (2S,3R,4R)-3-benzyloxy-2-iodomethyltetrahydrofuran-4-ol 
• 98-88-4 benzoyl chloride 

Downstream Products

• 373647-03-1 1-[(3R,4R,5R)-4-(benzyloxy)-5-(hydroxymethyl)tetrahydrofuran-3-yl]uracil 

Relevant academic research and scientific papers

Stereoselective synthesis of both enantiomers of 1,4-anhydro-alditols, 1,4-anhydro-2-amino-alditols and D- and L-isonucleosides from 2,3-O-isopropylidene-D-glyceraldehyde using iodine-induced cyclization as the key step

We have stereoselectively prepared the enantiomeric 1,4-anhydro-alditols (-)-15 and (+)-15, 1,4-anhydro-2-amino-aldi-tols (-)-19 and (+)-19, and isonucleosides (-)-22, (+)-22 and 25, from 2,3-O-isopropylidene-D-glyceraldehyde. The key step was the iodine-