ASYMMETRIC BROMOLACTONIZATION REACTION: SYNTHESIS OF OPTICALLY ACTIVE 2-HYDROXY-2-METHYLALKANOIC ACIDS FROM 2-METHYLENEALKANOIC ACIDS

DOI: 10.1016/S0040-4039(00)96213-0

Source and publish data:

Tetrahedron Letters p. 2801 - 2804 (1987)

Update date:2022-07-29

Topics:: Authors:

Corey, Paul F.

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Article abstract of DOI:10.1016/S0040-4039(00)96213-0

Optically pure 2-hydroxy-2-methylalkanoic acids of either configuration may be obtained via an asymmetric bromolactonization reaction using L-proline as a chiral auxilliary.

Full text of DOI:10.1016/S0040-4039(00)96213-0

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Article Doi

ASYMMETRIC BROMOLACTONIZATION REACTION: SYNTHESIS OF OPTICALLY ACTIVE 2-HYDROXY-2-METHYLALKANOIC ACIDS FROM 2-METHYLENEALKANOIC ACIDS

DOI: 10.1016/S0040-4039(00)96213-0

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)96213-0

Full text of DOI:10.1016/S0040-4039(00)96213-0

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