Tetrahedron: Asymmetry

Synthesis of chiral monoaza-15-crown-5 ethers from a chiral amino alcohol and enantiomeric recognition of potassium and sodium salts of amino acids

M Togrul, M Askin, H Hosgoren

Index: Togrul, Mahmut; Askin, Muzaffer; Hosgoren, Halil Tetrahedron Asymmetry, 2005 , vol. 16, # 16 p. 2771 - 2777

Full Text: HTML

Citation Number: 22

Abstract

The enantiomeric recognition of chiral monoaza-crown ethers for amino acids as their sodium and potassium salts has been investigated by UV–vis. The highest discrimination was observed for TrpK (d/l= 6.47). The reversed enantioselectivity of chiral monoaza-crown ether II was observed for TrpK.

Synthesis and pyrolytic behaviour of thiazolidin-2-one 1, 1-dioxides

[Aitken, R. Alan; Armstrong, David P.; Galt, Ronald H. B.; Mesher, Shaun T. E. Journal of the Chemical Society - Perkin Transactions 1, 1997 , # 14 p. 2139 - 2145]

Asymmetric reductions of ketones using lithium aluminium hydride modified with N, N-dialkyl derivatives of (R)-(−)-2-aminobutan-1-ol

[Brown, Eric; Penfornis, Annie; Bayma, Joaquim; Touet, Joeul Tetrahedron: Asymmetry, 1991 , vol. 2, # 5 p. 339 - 342]

Synthesis of chiral monoaza-15-crown-5 ethers from a chiral amino alcohol and enantiomeric recognition of potassium and sodium salts of amino acids

Abstract

Related Articles:

More Articles...