1Ager D J, Prakash I, Schaad D R. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis. Chem Rev, 1996, 96(2): 835~875
2Karrer P, Portmann P, Su:er M. L-Valinol und L-Tyrosinol. Helv Chim Acta, 1949, 32( Ⅲ ): 1156~1157
3Karrer P, Portmann P, Suter M. Die Reduktion von α-Aminocarbonsaureestern zu Aminoalkoholen Nitlels Lithiumaluminiumhydrid. Helv Chim Acta, 1948, 31(Ⅵ ): 1617~1623
4Vimal R C A. A Convenient and Mild Procedure for the Reduction of Amino Acids Using Amberlyst 15-NaBH4--LiCl. Tetrahedron Lett, 1998, 39(8): 917~918
5Falorni M, Porcheddu A, Taddei M. Mild Reduction of Carboxylic Acids to Alcohols Using Cyanuric Chloride and Sodium Borohydride. Tetrahedron Lett, 1999, 40(23): 4395~4396
6Ranu B C. Zinc Borohydride-A Reducing Agent with High Potential. Synlett, 1993, (12): 885~892
7Sudharshan M, Hultin P G. An Improved Preparation of Oxazolidin-2-One Chiral Auxiliaries. Synlett, 1997, (2): 171~172
8Segel E. Hydrogenation of Esters of L-Alanine and L-Leucine over Copper-Chromium Oxide Catalyst. J Am Chem Soc, 1952, 74(4): 1096
9Adkins H, Pavlic A A. Hydrogenation of Esters to Alcohols over Raney Nickel. J Am Chem Soc, 1947, 69(12): 3039~3041
10Adkins H, Billica H R. The Hydrogenation of Esters to Alcohols at 25~150℃. J Am Chem Soc, 1948, 70(9): 3121~3125