150653-80-8

Upstream product

• 164105-30-0 4,6-O-benzylidene-1,5:2,3-dianhydro-D-mannitol 
• 150571-95-2 Methanesulfonic acid (2R,4aR,7S,8aS)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 852235-04-2 (2R,4aR,7S,8aS)-2-Phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 
• 150571-93-0 1,5-anhydro-2,3-dideoxy-4,6-O-(phenylmethylene)-D-erythro-hex-1-enitol 
• 124-63-0 methanesulfonyl chloride 
• 149312-20-9 1',5'-anhydro-4,6-O-benzylidene-3-deoxy-D-glucitol 

Downstream Products

• 150571-93-0 1,5-anhydro-2,3-dideoxy-4,6-O-(phenylmethylene)-D-erythro-hex-1-enitol 
• 76231-50-0 (2R,4aR,8aS)-2-Phenyl-4,4a,8,8a-tetrahydro-pyrano[3,2-d][1,3]dioxine 
• 185021-11-8 (2R,3S,5S)-5-Amino-2-hydroxymethyl-tetrahydro-pyran-3-ol 

Relevant academic research and scientific papers

The synthesis of modified D- and L-anhydrohexitol nucleosides

The synthesis and antiviral activities of novel L-isomers 9-13 and modified D-guanine analogs 1d,e of recently reported anhydrohexitol nucleosides 1 are described. An efficient approach to known anhydrohexitol nucleoside precursor 2 from diacetone-D-glucose 3 is also reported.

Anomeric effect on kinetic acidity: Examples for the oxygen atom of ethers to accelerate abstraction of an α-hydrogen atom

In contrast with general observation, two different types of experiments indicate that the abstraction of α-hydrogen atom of ether having proper conformation is slightly enhanced by the oxygen atom in line with our previous AM1 calculation.