TY - JOUR
TI - A convenient one-step synthesis of stable β-amino alcohol N-boranes from α-amino acids
AU - Georgios Vougioukalakis
AU - Kyriakos Papadopoulos
AU - Afroditi Pinaka
AU - Dimitra Dimotikali
AU - Vassilis Psyharis
JO - SYNTHESE - DORDRECHT
PY - 2012
VL - 44
TODO - 07
SP - 1057--1062
PB - Georg Thieme Verlag KG
SN - 0039-7857
TODO - 10.1055/s-0031-1289727
TODO - -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
TODO - 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.
ER -