A highly stereoselective synthesis of (2S,3S)-β-hydroxyleucine

DOI: 10.1016/S0040-4039(97)00207-4

Source and publish data:

Tetrahedron Letters p. 1771 - 1772 (1997)

Update date:2022-08-04

Topics:

Authors:

Laib, Taoues

Chastanet, Jacqueline

Zhu, Jieping

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Article abstract of DOI:10.1016/S0040-4039(97)00207-4

A highly diastereoselective nucleophilic addition of Grignard reagent to N,N-dibenzyl-O-TBS-serinal 3 was the key step in the present synthesis of (2S,3S)-β-hydroxyleucine 1.

Full text of DOI:10.1016/S0040-4039(97)00207-4

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