The Synthesis of the δ-Lactone Portion of the Mevinic Acids; a New Non-acidic Method of Cyclic Lactone Expansion

DOI: 10.1039/c39880001417

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1417 - 1418 (1988)

Update date:2022-07-31

Topics: Synthesis Expansion δ-Lactone

Authors:

Davidson, Alan H.

Floyd, Chris D.

Lewis, Christopher N.

Myers, Peter. L.

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Article abstract of DOI:10.1039/c39880001417

An alkoxy-mercuration demercuration sequence has been used as the key step in an enantiospecific synthesis of a protected synthon for the lactone portion of the mevinic acids.

Full text of DOI:10.1039/c39880001417

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