A FACILE ONE-STEP SYNTHESIS OF β,γ-UNSATURATED CABOXYLIC ACID ESTERS VIA 1,2-CARBONYL TRANSPOSITIONS OF α,β-UNSATURATED KETONES

DOI: 10.1016/S0040-4039(00)97463-X

Source and publish data:

Tetrahedron Letters p. 3757 - 3758 (1990)

Update date:2022-07-29

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Authors:

Mathew, Felix

Myrboh, B.

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Article abstract of DOI:10.1016/S0040-4039(00)97463-X

Reaction of α,β-unsaturated ketone, 1, with lead(IV)acetate and borontrifluoride etherate in the presence of methanol yielded the β,γ-unsaturated esters, 2, in a single step procedure, at room temperature.

Full text of DOI:10.1016/S0040-4039(00)97463-X

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