Synthesis of d-Fagomine and Its Seven- and Eight-Membered Higher-Ring Analogues, and the Formal Synthesis of (+)-Australine from l-Xylose-Derived Chiron

^‡ These authors contributed equally to this work.

Abstract

The synthesis of d-fagomine and its seven- and eight-membered higher-ring analogues from commercially available l-xylose is reported. The syntheses involve elaboration of a common alkenol precursor obtained from l-xylose-derived hemiacetal. The key steps in the syntheses are intramolecular reductive amination and ring-closing metathesis for the synthesis of d-fagomine and seven-/eight-membered iminosugar, respectively. We have also extended our synthetic strategy for the formal synthesis of (+)-australine using zinc-mediated fragmentation reaction and ring-closing metathesis as key steps.

Key words

d-fagomine - aminocyclitols - metathesis - (+)-australine - reductive amination

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