Journal of the Chemical Society. Chemical communications p. 169 - 171 (1981)
Update date:2022-08-28
Topics:
Ahmad, Faujan B. H.
Bruce, J. Malcolm
Khalafy, Jabbar
Sabetian, Khojasteh
Treatment of the Diels-Alder adduct 4a-acetyl-4a,5,8,8a-tetrahydro-3-methyl-1,4-naphthoquinone with pyridine-methanol or acetic anhydride leads to a <1,5> acetyl shift to the 3-position which can be followed by a <1,2> acetyl shift to the 2-position (adduct numbering).
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