Literature DB >> 24193031

A fast and simplein situ method for the determination of the absolute configuration of amino acid esters using the chiroptical properties of their Eu(FOD)3 complexes.

V Toome1, B Wegrzynski.   

Abstract

The NMR shift reagent, Europium(III)-tris-(1,1,1,2,2,3,3)-heptafluoro-7,7-dimethyl-4-6-octanedione [Eu(fod)3], complexes efficiently withα-amino acid esters in chloroform. These complexes exhibit characteristic circular dichroism (CD) spectral patterns in the 350-250 nm region. A fast and simple procedure (also in microscale) has been worked out which utilizes the signs of these CD bands for the determination of the absolute configuration at theα-carbon atomin situ. In the L-series, a positive CD band is observed at around 310 nm and a negative one in the 290-280 nm region. The CD spectra of the Eu complexes of the D-isomers are mirror images of those of the L-configurations. An empirical rule is proposed.

Entities:  

Year:  1992        PMID: 24193031     DOI: 10.1007/BF00806784

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  4 in total

1.  A stereoselective synthesis of the 24(R),25-dihydroxycholesterol side chain.

Authors:  J J Partridge; V Toome; M R Uskokovic
Journal:  J Am Chem Soc       Date:  1976-06-09       Impact factor: 15.419

2.  Conformational equilibria and stereochemical relationships among carboxylic acids.

Authors:  I Listowsky; G Avigad; S Englard
Journal:  J Org Chem       Date:  1970-04       Impact factor: 4.354

3.  Optical activity of aromatic chromophores. I. O, m, and p-tyrosine.

Authors:  T M Hooker; J A Schellman
Journal:  Biopolymers       Date:  1970-11       Impact factor: 2.505

4.  Absolute configurational studies of vicinal glycols and amino alcohols. I. With ni(acac)2.

Authors:  J Dillon; K Nakanishi
Journal:  J Am Chem Soc       Date:  1975-09-17       Impact factor: 15.419

  4 in total

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