Efficient procedure for the reduction of alpha-amino acids to enantiomerically pure alpha-methylamines.
DA Quagliato, PM Andrae…
Index: Journal of Organic Chemistry, , vol. 65, # 16 p. 5037 - 5042
Full Text: HTML
Citation Number: 29
Abstract
1. J Org Chem. 2000 Aug 11;65(16):5037-42. Efficient procedure for the reduction of alpha-amino acids to enantiomerically pure alpha-methylamines. Quagliato DA(1), Andrae PM, Matelan EM. Author information: (1)Department of Chemical Sciences, Wyeth-Ayerst Research ...
Related Articles:
An efficient synthesis of (-)-deacetylanisomycin starting from D-tyrosine
[Synthesis, , # 13 p. 1867 - 1870]
Enzymatic peptide syntheses in organic solvent mediated by modified α-chymotrypsin
[Tetrahedron Letters, , vol. 30, # 21 p. 2787 - 2790]
Synthesis of novel and photolabile philanthotoxin analogs: glutamate receptor antagonists
[Tetrahedron, , vol. 48, # 23 p. 4793 - 4822]