Carboindation of alkynols. A facile synthesis of yomogi alcohol

DOI: 10.1016/S0040-4039(00)92248-2

Source and publish data:

Tetrahedron Letters p. 2581 - 2582 (1992)

Update date:2022-08-05

Topics:

Authors:

Araki, Shuki

Imai, Akira

Shimizu, Ken

Butsugan, Yasuo

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Article abstract of DOI:10.1016/S0040-4039(00)92248-2

Carboindation of alkynols by ally lie indium sesquihalides proceeded in DMF at 100 - 140 °C via a synaddition; yomogi alcohol was prepared in onepot by this method.

Full text of DOI:10.1016/S0040-4039(00)92248-2

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Product name:3,6-Heptadien-2-ol, 2-methyl-5-phenyl-, (E)-

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