4.7 Article

Asymmetric Synthesis of Cyclic cis-β-Amino Acid Derivatives Using Sulfinimines and Prochiral Weinreb Amide Enolates

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 75, Issue 11, Pages 3814-3820

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo100680b

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Funding

  1. National Institutes of General Medicinal Sciences [GM 57870]

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Cyclic cis-beta-amino Weinreb amides, valuable building blocks for the asymmetric synthesis of cyclic beta-amino acids derivatives, are readily prepared via ring-closing metathesis of sulfinimine-derived N-sulfinyl beta-amino diene Weinreb amides. These unsaturated cyclic cis-beta-amino Weinreb amides are valuable building blocks for the asymmetric synthesis of cyclic beta-amino acid derivatives.

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