Enantioselective alkylation of chiral enolates

Author: Evans, D. A.; Takacs, J. M.

Description: Alkylations of chiral amide enolates derived from (l)-prolinol have been shown to yield versatile hydroxy-amides in high diastereomeric purity. Their use in the preparation of optically active carboxylic acids is described.

Subject headings: Synthesis; Preparation; Chiral enolates; Alkylations; Carboxylic acids

Publication year: 1980

Journal or book title: Tetrahedron Letters

Volume: 21

Issue: 44

Pages: 4233-4236

Find the full text: https://www.sciencedirect.com/science/article/abs/pii/S0040403900928703

Find more like this one (cited by): https://scholar.google.com/scholar?cites=3412045973987953398&as_sdt=1000005&sciodt=0,16&hl=en

Serial number: 3544

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