The ester dienolate [2,3]-Wittig rearrangement. Diastereoselective synthesis of 2,3-dialkenyl-substituted 2-hydroxy-γ-lactones

DOI: 10.1016/S0040-4020(99)00019-8

Source and publish data:

Tetrahedron p. 2625 - 2638 (1999)

Update date:2022-07-29

Topics:: Authors:

Hiersemann, Martin

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Article abstract of DOI:10.1016/S0040-4020(99)00019-8

The ester dienolate [2,3]-Wittig rearrangement proceeds with high yield and anti/syn diastereoselection to afford 3-alkoxycarbonyl-3-hydroxy- substituted 1,5-hexadienes. No donor solvent or metal salt additive was necessary to trigger the rearrangement. T

Full text of DOI:10.1016/S0040-4020(99)00019-8

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Article Doi

The ester dienolate [2,3]-Wittig rearrangement. Diastereoselective synthesis of 2,3-dialkenyl-substituted 2-hydroxy-γ-lactones

DOI: 10.1016/S0040-4020(99)00019-8

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4020(99)00019-8

Full text of DOI:10.1016/S0040-4020(99)00019-8

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