STEREOSELECTIVE SYNTHESIS OF THE OPTICALLY ACTIVE FUNCTIONALIZED 1,3,5-ALL-ANTI-TRIOL

DOI: 10.1016/S0040-4039(00)98471-5

Source and publish data:

Tetrahedron Letters p. 75 - 78 (1985)

Update date:2022-08-03

Topics:

Authors:

Nakata, Tadashi

Nagao, Shigeto

Oishi, Takeshi

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Article abstract of DOI:10.1016/S0040-4039(00)98471-5

The optically active 1,3,5-all-anti-triol 20 was synthesized starting from (S)-(-)-malic acid with complete stereoselection, based on the stereoselective reduction of cyclic β-keto acetal and successive transthioacetalization.

Full text of DOI:10.1016/S0040-4039(00)98471-5

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