Enantioselective preparation of 1-benzyloxy-3-methyl-6-heptene-2,4-diols: Total synthesis of (+)-prelactone C

DOI: 10.1016/S0040-4039(97)01042-3

Source and publish data:

Tetrahedron Letters p. 4823 - 4826 (1997)

Update date:2022-07-29

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Authors:

Esumi, Tomoyuki

Fukuyama, Hiroko

Oribe, Reiko

Kawazoe, Kaori

Iwabuchi, Yoshiharu

Irie, Hiroshi

Hatakeyama, Susumi

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Article abstract of DOI:10.1016/S0040-4039(97)01042-3

A concise method leading to all stereoisomers of 1-benzyloxy-3-methyl-6-heptene-2,4-diol from (2E,5E)-1,7-dibenzyloxy-2,5-heptadiene-4-ol has been developed. The first synthesis of (+)-prelactone C, a δ-lactone isolated from the concanamycin-producing Str

Full text of DOI:10.1016/S0040-4039(97)01042-3

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