A highly stereoselective synthesis of (2S, 3S)-β-hydroxyleucine
作者:Taoues Laïb、Jacqueline Chastanet、Jieping Zhu
DOI:10.1016/s0040-4039(97)00207-4
日期:1997.3
A highly diastereoselective nucleophilic addition of Grignard reagent to N,N-dibenzyl-O-TBS-serinal3 was the key step in the present synthesis of (2S, 3S)-β-hydroxyleucine1.
Diastereoselective Synthesis of γ-Hydroxy-β-amino Alcohols and (2<i>S</i>,3<i>S</i>)-β-Hydroxyleucine from Chiral <scp>d</scp>-(<i>N,N</i>-Dibenzylamino)serine (TBDMS) Aldehyde