Enzymatic resolution of 1,1-dimethoxybut-3-en-2-ol and 1,1-dimethoxypent-4-en-2-ol, alpha-hydroxyaldehyde precursors for aldol-type reactions - Archive ouverte HAL
Article Dans Une Revue Tetrahedron: Asymmetry Année : 2005

Enzymatic resolution of 1,1-dimethoxybut-3-en-2-ol and 1,1-dimethoxypent-4-en-2-ol, alpha-hydroxyaldehyde precursors for aldol-type reactions

Résumé

Hydroxyacetals 2 and 3 were resolved by acylation with vinyl acetate in the presence of lipases in organic media. The reverse reaction, the enzymatic hydrolysis of the corresponding acetates, was also highly stereoselective and provided the opposite enantiomers

Domaines

Chimie organique
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Dates et versions

hal-00125718 , version 1 (02-03-2007)

Identifiants

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R. Chenevert, S. Gravil, Jean Bolte. Enzymatic resolution of 1,1-dimethoxybut-3-en-2-ol and 1,1-dimethoxypent-4-en-2-ol, alpha-hydroxyaldehyde precursors for aldol-type reactions. Tetrahedron: Asymmetry, 2005, pp.2081-2086. ⟨10.1016/j.tetasy.2005.05.013⟩. ⟨hal-00125718⟩
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