MAGNESIUM-OPPENAUER OXIDATION OF ALCOHOLS TO ALDEHYDES AND KETONES

DOI: 10.1016/S0040-4039(01)80985-0

Source and publish data:

Tetrahedron Letters p. 769 - 772 (1987)

Update date:2022-08-31

Topics:

Authors:

Byrne, Brian

Karras, Michael

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Article abstract of DOI:10.1016/S0040-4039(01)80985-0

Using a magnesium-Oppenauer oxidation aldehydes and ketones are prepared from halomagnesium alkoxides, which in turn are the products of Grignard reactions.

Full text of DOI:10.1016/S0040-4039(01)80985-0

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