Electroreductively promoted diastereoselective coupling of ketones with allylic alcohols. Synthesis of optically active 1,4-diols

DOI: 10.1021/jo00081a001

Source and publish data:

Journal of Organic Chemistry p. 273 - 275 (1994)

Update date:2022-07-30

Topics:

Authors:

Shono Shono

Morishima

Moriyoshi

Ishifune

Kashimura

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Article abstract of DOI:10.1021/jo00081a001

Cathodic coupling of ketones with allylic alcohols has been found to take place with high regio- and stereoselectivities at the position γ to the hydroxyl group to afford the corresponding 1,4-diols.

Full text of DOI:10.1021/jo00081a001

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