The first enantiocontrolled synthesis of (3S,8S)-(-)-4,6-decadiyne-1,3,8-triol isolated from a toxic mushroom Gymnopilus spectabilis

DOI: 10.1016/0040-4039(91)85089-N

Source and publish data:

Tetrahedron Letters p. 2797 - 2798 (1991)

Update date:2022-07-29

Topics:

Authors:

Takano Takano

Sugihara

Ogasawara

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Article abstract of DOI:10.1016/0040-4039(91)85089-N

The first synthesis of (3S,8S)-(-)-4,6-decadiyne-1,3,8-triol, isolated from a toxic mushroom Gymnopilus spectabilis, has been achieved by employing the chiral 3-hydroxyalkyne formation reaction as the key step.

Full text of DOI:10.1016/0040-4039(91)85089-N

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