Aldol Reaction of 4-Trimethylsiloxy-6-methylene-1,3-dioxines with Chiral Aldehydes: Enantioselective Synthesis of 1,3-Dioxin-4-ones Having a 2,3-Dihydroxylated Alkyl Group at the 6-Position

DOI: 10.1016/S0957-4166(00)82101-1

Source and publish data:

Tetrahedron Asymmetry p. 1157 - 1160 (1992)

Update date:2022-07-29

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Authors:

Sato, Masayuki

Sugita, Yoshiaki

Abiko, Yumi

Kaneko, Chikara

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Article abstract of DOI:10.1016/S0957-4166(00)82101-1

A novel enantioselective synthesis of 1,3-dioxin-4-ones having a 2,3-dihydroxylated alkyl group at the 6-position has been accomplished by titanium tetrachloride-mediated aldol condensation of silyl enol ethers derived from the 6-alkylated dioxinones with

Full text of DOI:10.1016/S0957-4166(00)82101-1

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