Stereoselective Synthesis of Enamides by a Peterson Reaction Manifold

Alois Fürstner, Christof Brehm, Yolanda Cancho‐Grande

Organic Letters · 2001 · 83 citations · 20 references

Concepts

Abstract

Vinylsilanes are converted into enamides by a sequence comprising epoxidation, nucleophilic ring opening of the resulting epoxysilanes with NaN(3), and reduction of the azide, followed by a "one-pot" N-acylation/Peterson elimination process. This method is distinguished by its wide applicability and stereoselective course. [reaction: see text]

References

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