NOVEL OXIDATIVE REARRANGEMENT OF β,γ-UNSATURATED KETONE HYDRAZONES ON IODINATION IN BASE

DOI: 10.1016/S0040-4039(00)88677-3

Source and publish data:

Tetrahedron Letters p. 3991 - 3994 (1982)

Update date:2022-08-05

Topics:

Authors:

Jung, Michael E.

Hatfield, Gregory L.

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Article abstract of DOI:10.1016/S0040-4039(00)88677-3

Iodination of the bicyclic enone hydrazone 3 in excess triethylamine gave, in addition to the expected vinyl iodide 4, the rearranged aromatic product 5.

Full text of DOI:10.1016/S0040-4039(00)88677-3

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