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Synthesis 2012(7): 1057-1062
DOI: 10.1055/s-0031-1289727
DOI: 10.1055/s-0031-1289727
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
A Convenient One-Step Synthesis of Stable β-Amino Alcohol N-Boranes from α-Amino Acids
Further Information
Received
23 January 2012
Publication Date:
27 February 2012 (online)
Publication History
Publication Date:
27 February 2012 (online)
Abstract
Novel, non-cyclic β-amino alcohol N-boranes are isolated from the sodium borohydride-sulfuric acid assisted direct reduction of a series of α-amino acids. The reduction takes place in one step under mild conditions and affords the products in good yields.
Key words
amino acids - β-amino alcohols - reduction - sodium borohydride - β-amino alcohol N-boranes
- Supporting Information for this article is available online:
- Supporting Information
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