STEREOSELECTIVE REDUCTION OF β-KETO ESTERS WITH ZINC BOROHYDRIDE. STEROSELECTIVE SYNTHESIS OF ERYTHRO-3-HYDROXY-2-ALKYLPROPIONATES

DOI: 10.1016/S0040-4039(00)77774-4

Source and publish data:

Tetrahedron Letters p. 1641 - 1644 (1980)

Update date:2022-09-26

Topics: Synthesis Reduction Stereoselective β-keto esters

Authors:

Nakata, Tadashi

Oishi, Takeshi

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Article abstract of DOI:10.1016/S0040-4039(00)77774-4

Erythro-3-hydroxy-2-alkylpropionates were prepared in high stereoselectivity and in high isolated yield by zinc borohydride reduction of the corresponding β-keto esters.

Full text of DOI:10.1016/S0040-4039(00)77774-4

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