Enantioselective Synthesis of trans-Whisky Lactone by Using Newly Developed Asymmetric Ring Expansion Reaction of Oxetane as a Key Step

DOI: 10.1246/cl.1995.1027

Source and publish data:

Chemistry Letters p. 1027 - 1028 (1995)

Update date:2022-07-29

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Authors:

Ito, Katsuji

Yoshitake, Miwa

Katsuki, Tsutomu

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Article abstract of DOI:10.1246/cl.1995.1027

A mixture of optically active 3-substituted cis- and trans-tetrahydrofuran-2-carboxylates which was prepared in one step from readily available (+/-)-2-alkynyloxetane, was converted into trans-whisky lactone (2) in a straightforward manner.

Full text of DOI:10.1246/cl.1995.1027

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