UNSATURATED CARBOXYLIC ACID DIENOLATES. MICHAEL ADDITION TO ENONES THROUGH TANDEM 1,2-ADDITION - OXY-COPE REARRANGEMENT.

DOI: 10.1016/S0040-4039(00)94860-3

Source and publish data:

Tetrahedron Letters p. 2485 - 2488 (1985)

Update date:2022-08-05

Topics:

Authors:

Ballester, P.

Garcia-Raso, A.

Gomez-Solivellas, A.

Mestres, R.

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Article abstract of DOI:10.1016/S0040-4039(00)94860-3

Michael addition of the dienolate derived from 2-butenoic acid to 1,3-diphenylpropenone occurs through a 1,2-addition followed by a <3,3>-sigmatropic rearrangement, α,γ-regioselectivity found for Michael addition to other styryl ketones depends on the ste

Full text of DOI:10.1016/S0040-4039(00)94860-3

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