Literature DB >> 25510928

An ESI-MS method to determine yield and enantioselectivity in a single assay.

Maureen E Smith1, Steven A Knolls, MyLe Thompson, Douglas S Masterson.   

Abstract

A mass spectrometry assay is presented here that allows for the simultaneous determination of yield and enantioselectivity in a single analysis. The assay makes use of molecules that are structurally similar to the analytes of interest as standards. The assay predicts the yields of the reactions reasonably well and with little error. For example, in the pig liver esterase catalyzed hydrolysis of one prochiral malonate, the yield predicted by the assay was 72%, while larger scale isolated reaction yields were within 5% of this value. This assay provides a fast method to determine yield and enantioselectivity in one analysis. The strengths and limitations of this method are discussed.

Entities:  

Year:  2014        PMID: 25510928     DOI: 10.1007/s13361-014-1041-6

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  28 in total

1.  Toward the creation of NMR databases in chiral solvents: bidentate chiral NMR solvents for assignment of the absolute configuration of acyclic secondary alcohols.

Authors:  Yoshihisa Kobayashi; Nobuyuki Hayashi; Yoshito Kishi
Journal:  Org Lett       Date:  2002-02-07       Impact factor: 6.005

2.  Isotopically chiral probes for in situ high-throughput asymmetric reaction analysis.

Authors:  Michael A Evans; James P Morken
Journal:  J Am Chem Soc       Date:  2002-08-07       Impact factor: 15.419

3.  Mass spectrometric screening of chiral catalysts and catalyst mixtures.

Authors:  Constanze Annelie Müller; Christian Markert; Antje Maria Teichert; Andreas Pfaltz
Journal:  Chem Commun (Camb)       Date:  2009-02-19       Impact factor: 6.222

4.  A comparison of quantitative nuclear magnetic resonance methods: internal, external, and electronic referencing.

Authors:  Christopher H Cullen; G Joseph Ray; Christina M Szabo
Journal:  Magn Reson Chem       Date:  2013-09-03       Impact factor: 2.447

5.  Determination of analyte concentration using the residual solvent resonance in (1)H NMR spectroscopy.

Authors:  Gregory K Pierens; Anthony R Carroll; Rohan A Davis; Meredith E Palframan; Ronald J Quinn
Journal:  J Nat Prod       Date:  2008-04-05       Impact factor: 4.050

6.  Characterization of the isoenzymes of pig-liver esterase. 1. Chemical Studies.

Authors:  E Heymann; W Junge
Journal:  Eur J Biochem       Date:  1979-04

7.  Stereodynamic chemosensor with selective circular dichroism and fluorescence readout for in situ determination of absolute configuration, enantiomeric excess, and concentration of chiral compounds.

Authors:  Keith W Bentley; Christian Wolf
Journal:  J Am Chem Soc       Date:  2013-08-06       Impact factor: 15.419

8.  A facile circular dichroism protocol for rapid determination of enantiomeric excess and concentration of chiral primary amines.

Authors:  Sonia Nieto; Justin M Dragna; Eric V Anslyn
Journal:  Chemistry       Date:  2010-01-04       Impact factor: 5.236

9.  A stereoselective cyclization strategy for the preparation of γ-lactams and their use in the synthesis of α-methyl-β-proline.

Authors:  Souvik Banerjee; Justin Smith; Jillian Smith; Caleb Faulkner; Douglas S Masterson
Journal:  J Org Chem       Date:  2012-11-12       Impact factor: 4.354

10.  Facile quantification of enantiomeric excess and concentration with indicator-displacement assays: an example in the analyses of alpha-hydroxyacids.

Authors:  Lei Zhu; Eric V Anslyn
Journal:  J Am Chem Soc       Date:  2004-03-31       Impact factor: 15.419

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