A highly diastereoselective "super silyl" governed aldol reaction: Synthesis of α,β-dioxyaldehydes and 1,2,3-triols

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Abstract

A highly diastereoselective approach for the synthesis of protected α,β-dioxyaldehydes derived from (Z)-tris(trimethylsilyl)silyl "super silyl" enol ethers is described. A general and highly syn-stereoselective aldol reaction directed by the "super silyl" group catalyzed by triflimide (HNTf 2 ) is developed providing α,β-dioxyaldehydes and 1,2,3-triol fragments which can be a useful platform for the elaboration of natural and unnatural sugar derivatives.

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Gati, W., & Yamamoto, H. (2016). A highly diastereoselective “super silyl” governed aldol reaction: Synthesis of α,β-dioxyaldehydes and 1,2,3-triols. Chemical Science, 7(1), 394–399. https://doi.org/10.1039/c5sc03307a

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