Quinone methide from 4-hydroxybenzyl alcohol diacetate: (P-acetoxy)benzylation of β-dicarbonyls

DOI: 10.1016/S0040-4039(00)79074-5

Source and publish data:

Tetrahedron Letters p. 5287 - 5290 (1992)

Update date:2022-07-30

Topics:

Authors:

Sanner, Mark A.

Stansberry, Mary

Weigelt, Carolyn

Michne, William F.

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Article abstract of DOI:10.1016/S0040-4039(00)79074-5

Diacetate 1c is a readily available quinone methide equivalent when treated with Cs₂CO₃ for C-(p)-acetoxy)benzylation of β-dicarbonyls in 51-89 % yield.

Full text of DOI:10.1016/S0040-4039(00)79074-5

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