1213233-82-9Relevant academic research and scientific papers
Asymmetric synthesis of all stereoisomers of a-methylthreonine using an organocatalytic steglich rearrangement reaction as a key step
Dietz, Friedrich R.,Groeger, Harald
, p. 4208 - 4218 (2011/04/12)
An efficient synthetic route to all four stereoisomers of a-methylthreonine has been established. Each type of stereoisomer has been isolated in diastereomerically pure form and with an enantiomeric excess of at least 86% ee. The key step in this multi-st
