NoteRegioselective sulfonylation at O-2 of cyclomaltoheptaose with 1-(p-tolylsulfonyl)-(1H)-1,2,4-triazole-Science-Chemical Encyclopedia-lookchem

NoteRegioselective sulfonylation at O-2 of cyclomaltoheptaose with 1-(p-tolylsulfonyl)-(1H)-1,2,4-triazole
Add time:08/24/2019 Source:sciencedirect.com

2I-O-p-Tolylsulfonylcyclomaltoheptaose was obtained in 42% yield by reaction of 1-(p-tolylsulfonyl)-(1H)-1,2,4-triazole on NaH-deprotonated cyclomaltoheptaose in DMF and further converted into the corresponding mono-2I,3I-manno-epoxide.

We also recommend Trading Suppliers and Manufacturers of 6(1),6(3)-di-O-(alpha-glucopyranosyl)cyclomaltoheptaose (cas 104723-61-7). Pls Click Website Link as below: cas 104723-61-7 suppliers

Prev:Application of ultra-high magnetic field for saccharide molecules: 1H NMR spectra of 6-O-α-d-glucopyranosyl-cyclomaltoheptaose and -cyclomaltohexaose
Next: Preparation and reactivity of a novel disaccharide, glucosyl 1,5-anhydro-d-fructose (1,5-anhydro-3-O-α-glucopyranosyl-d-fructose))

Click to view details

Health and Chemicalmore >