106192-93-2

Upstream product

• 108-24-7 acetic anhydride 
• 32445-72-0 1,6-di-O-(p-toluenesulfonyl)-2,5-anhydro-L-iditol 
• 65729-86-4 1,3,4,6-tetra-O-acetyl-2,5-anhydro-D-glucitol 
• 27826-73-9 2,5-anhydro-D-glucitol 
• 22144-41-8 2,5-anhydro-1,6-di-O-benzoyl-D-glucitol 
• 32445-72-0 2,5-anhydro-1,6-di-O-p-tolylsulfonyl-D-glucitol 

Downstream Products

• 88777-23-5 3,4-di-O-acetyl-2,5-anhydro-1,6-diazido-1,6-dideoxy-D-glucitol 

Relevant academic research and scientific papers

Mono- and Dioxetanes of 2,5-Anhydroalditols, Syntheses and Reactions

Starting from appropriate 2,5-anhydroalditols the monooxetanes 3, 9, 15, and 20 have been prepared by selective monotosylation of primary hydroxy groups and subsequent treatment with base.Analogous reactions gave the 1,3:2,5:4,6-trianhydrohexitols 10 and

SYNTHESIS OF 6-AMINO-2,5-ANHYDRO-6-DEOXY-AND -1,6-DIDEOXY-D-GLUCITOL AND SOME DERIVATIVES THEREOF

6-Amino-2,5-anhydro-6-deoxy- and -1,6-dideoxy-D-glucitol (44), as well as some of their derivatives, were synthesized, starting from D-mannitol. 3,4-Di-O-allyl-1,2:5,6-dianhydro-D-mannitol was converted into the 2,5-anhydro-6-bromo compound 8, the bromine