Issue 4, 1981

[1,5] and [1,2] Acetyl shifts in Diels–Alder adducts of 2-acetyl-6-methyl-1,4-benzoquinone

Abstract

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).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 169-171

[1,5] and [1,2] Acetyl shifts in Diels–Alder adducts of 2-acetyl-6-methyl-1,4-benzoquinone

F. B. H. Ahmad, J. M. Bruce, J. Khalafy and K. Sabetian, J. Chem. Soc., Chem. Commun., 1981, 169 DOI: 10.1039/C39810000169

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