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Chiral aminophosphonate eluent for enantiomeric analysis of amino acids

โœ Scribed by Yuri P. Belov; Alexei Y. Aksinenko; Bernard Blessington; Amy H. Newman


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
319 KB
Volume
8
Category
Article
ISSN
0899-0042

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โœฆ Synopsis


An aqueous solution of the (+)-monoethyl ester of N-(1'-hydroxymethyl-)propyl-a-aminobenzylphosphonic acid has been proposed as a suitable chiral eluent for enantiomeric analysis of amino acids by ligand-exchange chromatography. Asymmetric synthesis of the chiral selector using (-)-(R)-2-aminobutan-l-ol as a starting reactant is de-


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Enantiomeric Separation of (ยฑ)-Amino Aci
โœ Kwang-Pill Lee; Hyun-Bong Lee; Young Cheol Lee; Seong-Ho Choi; Jae Jeong Ryoo; J ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 40 KB

The 3,5-dinitrobenzoyl (ฯฎ)-amino acid esters were successfully resolved on (ฯช)-phenylurea chiral stationary phases (CSPs) in a normal phase mode by high-performance liquid chromatography (HPLC). The alcohols used for esterification were methanol, ethanol, and n-propanol. The effects of esterificatio