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Merck
CN
  • Stereoselective synthesis of fully protected (2S,4S,6S)-2-amino-6-hydroxy-4-methyl-8-oxodecanoic acid (AHMOD).

Stereoselective synthesis of fully protected (2S,4S,6S)-2-amino-6-hydroxy-4-methyl-8-oxodecanoic acid (AHMOD).

Journal of peptide science : an official publication of the European Peptide Society (2012-01-18)
Wei Zhang, Xiangpeng Li, Ning Ding, Yingxia Li
摘要

The stereocontrolled synthesis of fully protected (2S,4S,6S)-2-amino-6-hydroxy-4-methyl-8-oxodecanoic acid was accomplished using a glutamate derivative as starting material. The key steps of this stereochemical synthetic pathway involved an Evans asymmetric alkylation, a Sharpless asymmetric epoxidation, and a Grignard reaction.

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Sigma-Aldrich
癸酸, ≥98.0%
Sigma-Aldrich
癸酸, ≥99.5%, FCC, FG
Sigma-Aldrich
癸酸钠, ≥98%
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癸酸, natural, ≥98%, FCC, FG
Supelco
癸酸, analytical standard