A safe, simple, one-pot preparation of N-derivatized β-amino alcohols and oxazolidinones from amino acids

Article abstract of DOI:10.1080/00397919108020783

N-tert-Butoxycarbonyl, N-benzoyl, N-benzyloxycarbonyl, and oxazilidinone derivatives of β-amino alcohols have been prepared from amino acids in 72 to 91% yields through lithium aluminum hydride reduction followed by in situ derivatization.

Full text of DOI:10.1080/00397919108020783

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Safe, Simple, One-Pot
Preparation of N-Derivatized
β-Amino Alcohols and
Oxazolidinones from Amino
Acids
Arlene Correa a , Jean-Noël Denis a & Andrew E.
Greene a
a Université Joseph Fourier de Grenoble, LEDSS, Bât.
52, 38041, Grenoble, Cedex, France
Published online: 24 Sep 2006.
To cite this article: Arlene Correa , Jean-Noël Denis & Andrew E. Greene (1991):
A Safe, Simple, One-Pot Preparation of N-Derivatized β-Amino Alcohols and
Oxazolidinones from Amino Acids, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 21:1, 1-9
To link to this article: http://dx.doi.org/10.1080/00397919108020783
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