Easy Access to Sauropunols A-D: Synthesis and Spectroscopy Correlation of Their Natural Methyl and Ethyl Glycosides.

3,6-Anhydro-2-deoxy-hexofuranoside, the natural product core, is present in natural sauropunols (A-D) and in their natural methyl and ethyl glycosides, now, namely, sauropunol H and sauropunol F. The easily synthesized d-glucose-derived 3,6-anhydro-1,2- O -isopropylidene-5- O -benzoyl-α-d-glucofuranose was elaborated to final targets employing the TsOH·H 2 O-catalyzed glycosylation reaction with seven different alcohols, subsequent radical deoxygenation, and appropriate deprotection reactions involving mild conditions with excellent functional group tolerance. A short total synthesis of sauropunols (A-D), sauropunol H, and the first total synthesis of sauropunol F are reported herein. The correlation of spectroscopy data of sauropunol H and sauropunol F has been derived through these syntheses.