Silyl Migrations in d‑Xylose Derivatives: Total Synthesis of a Marine Quinoline Alkaloid

Abstract

A versatile method for the synthesis of orthogonally protected d-xylose 1-thioethers is described using unusual silyl group migrations which were pivotal in the synthesis of 4,8-dimethyl-6-<i>O</i>-(2′,4′-di-<i>O</i>-methyl-β-d-xylopyranosyl)hydroxyquinoline confirming the structure and absolute configuration of the natural product

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Last time updated on 12/02/2018

This paper was published in FigShare.

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