doi: 10.1021/ol048936q.
A stereodivergent approach to amino acids, amino alcohols, or oxazolidinones of high enantiomeric purity
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- PMID: 15281773
- DOI: 10.1021/ol048936q
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A stereodivergent approach to amino acids, amino alcohols, or oxazolidinones of high enantiomeric purity
Org Lett.
.
Erratum in
- Org Lett. 2005 Apr 14;7(8):1673. Gobdout, Cédrickx [corrected to Godbout, Cédrickx]
Abstract
(-)-Menthone, an inexpensive chiral auxiliary, was used to prepare both enantiomers of alpha-amino acids, amino alcohols, or oxazolidinones. The sequence includes the S(N)2' displacement by a cuprate reagent and a Curtius rearrangement as key steps.
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