A mild and efficient approach to enantioenriched α-hydroxyethyl α,β-unsaturated δ-lactams
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文摘

A mild approach toward α-hydroxyethyl α,β-unsaturated δ-lactams is described.

The stereochemistry at the δ-position of the lactam was formed by Ellman’s protocol.

The α,β-unsaturated δ-lactam was smoothly constructed by ring-closing metathesis.

A Baylis–Hillman reaction afforded the substitution at the α-position of the lactam.

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