20325-18-2

Upstream product

• 20204-80-2 [(1R,2S,3S,4R,5R)-3-hydroxy-4-(p-tolylsulfonyl)-6,8-dioxabicyclo[3.2.1]oct-2-yl]-4-methylbenzenesulfonic acid 
• 498-07-7 levoglucosan 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 916676-55-6 3-C-allyl-1,6-anhydro-2,4-di-O-tosyl-β-D-allopyranose 
• 916676-61-4 1,6-anhydro-4-deoxy-3-C,4-N-(propane-1,3-diyl)-2-O-tosyl-4-tosylamino-β-D-gulopyranose 
• 916676-56-7 1,6-anhydro-3-(3-hydroxypropyl)-2,4-di-O-tosyl-β-D-allopyranose 
• 916676-58-9 1,6-anhydro-3-C-(3-azidopropyl)-2,4-di-O-tosyl-β-D-allopyranose 
• 916676-59-0 3-C-(3-aminopropyl)-1,6-anhydro-2,4-di-O-tosyl-β-D-allopyranose 
• 916676-60-3 1,6-anhydro-2,4-di-O-tosyl-3-C-[3-(tosylamino)propyl]-β-D-allopyranose 

Relevant academic research and scientific papers

Open chain chiral macrolide building blocks by opening of deoxygenated 1,6-anhydrosugars with 1,3-propanedithiol

Chiral building blocks for macrolides and related natural products are obtained from 1,6-anhydrosugars by conversion of the bicyclic acetals 2 or 12 into the open chain chiral 1,3-dithianes 6 and 13. Branched precursors can be obtained by opening of the C