Carbohydrate Research Journal
Rhamnan and rhamnan sulfate are naturally occurring carbohydrates that have important biological functions and possible therapeutic applications, but studies are limited to the microheterogeneous mixtures from natural sources. This work reports the first synthesis of any sulfated rhamnan fragments and successful automation of the process with a recently developed automated solution-phase approach using N-iodosuccinimide/trimethylsilyl triflate (NIS/TMSOTf) promotor and levulinoyl ester deprotection conditions. The automated solution-phase activation/deprotection approach was initially able to create alpha 1 → 2, 1 → 3 type rhamnan di- and trisaccharide in moderate yields. Once these targets were achieved, a process to use SO3•pyridine complex in DMF for sulfation compatible with an automated solution-phase liquid handling system was developed and successfully applied to carbohydrate sulfation to create two rhamnan sulfate fragments with differing monosulfation patterns.
For details:
Automated solution-phase syntheses of alpha 1 → 2, 1 → 3 type rhamnans and rhamnan sulfate fragments
Victoria R.Kohout, Nicola L.B.Pohl
Indiana University, Department of Chemistry, 212 S. Hawthorne Drive, Bloomington, IN, 47405, United States
For more information about Chemspeed solutions:
Carbohydrate Research Journal
https://doi.org/10.1016/j.carres.2019.107829
© 2019 Elsevier Ltd. All rights reserved.
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