ENANTIOSELECTIVE ALKYLATION OF CHIRAL ENOLATES

DOI: 10.1016/S0040-4039(00)92870-3

Source and publish data:

Tetrahedron Letters p. 4233 - 4236 (1980)

Update date:2022-08-05

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Authors:

Evans, D. A.

Takacs, J. M.

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Article abstract of DOI:10.1016/S0040-4039(00)92870-3

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

Full text of DOI:10.1016/S0040-4039(00)92870-3

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