@article{2955704,
    title = "A convenient one-step synthesis of stable β-amino alcohol N-boranes from α-amino acids",
    author = "Georgios Vougioukalakis and Kyriakos Papadopoulos and Afroditi Pinaka and Dimitra Dimotikali and Vassilis Psyharis",
    journal = "SYNTHESE - DORDRECHT",
    year = "2012",
    volume = "44",
    number = "07",
    pages = "1057--1062",
    publisher = "Georg Thieme Verlag KG",
    issn = "0039-7857",
    doi = "10.1055/s-0031-1289727",
    keywords = "-amino alcohol N -boranes;  Amino alcohols;  Direct Reduction;  Good yield;  One step;  One step synthesis;  sodium borohydride, Amines;  Amino acids;  Boron compounds;  Hydrides;  Reduction;  Sodium;  Sulfuric acid, Alcohols, 2 amino 2 phenylethanol n borane;  2 amino 3 (1h indol 2 yl)propan 1 ol n borane;  2 amino 3 methylpentan 1 ol n borane;  2 amino 3 phenylpropan 1 ol n borane;  2 amino 4 methylpentan 1 ol n borane;  2 amino 4 methylsulfanylbutan 1 ol n borane;  alpha amino acid;  aminoalcohol;  borane derivative;  isoleucine;  leucine;  methionine;  phenylalanine;  phenylglycine;  sodium borohydride;  sulfuric acid;  tryptophan;  unclassified drug, article;  carbon nuclear magnetic resonance;  chemical structure;  heteronuclear single quantum coherence;  infrared spectroscopy;  mass spectrometry;  proton nuclear magnetic resonance;  synthesis;  X ray crystallography",
    abstract = "Novel, non-cyclic -amino alcohol N-boranes are isolated from the sodium borohydride-sulfuric acid assisted direct reduction of a series of -amino acids. The reduction takes place in one step under mild conditions and affords the products in good yields. © Georg Thieme Verlag Stuttgart · New York."
}