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Items: 1 to 20 of 536

2.

Enantiomer assays of amino acid derivatives using tertiary amine appended trans-4-hydroxyproline derivatives as chiral selectors in the gas phase.

Zu C, Woolfolk JA, Koscho ME.

Anal Chim Acta. 2010 Feb 19;661(1):60-6. doi: 10.1016/j.aca.2009.12.011. Epub 2009 Dec 21.

PMID:
20113716
4.

Quotient ratio method for quantitative enantiomeric determination by mass spectrometry.

Tao WA, Clark RL, Cooks RG.

Anal Chem. 2002 Aug 1;74(15):3783-9.

PMID:
12175167
5.
6.

Kinetic method for the simultaneous chiral analysis of different amino acids in mixtures.

Wu L, Andy Tao W, Cooks RG.

J Mass Spectrom. 2003 Apr;38(4):386-93.

PMID:
12717750
7.

Noncovalent interactions between ([18]crown-6)-tetracarboxylic acid and amino acids: electrospray-ionization mass spectrometry investigation of the chiral-recognition processes.

Gerbaux P, De Winter J, Cornil D, Ravicini K, Pesesse G, Cornil J, Flammang R.

Chemistry. 2008;14(35):11039-49. doi: 10.1002/chem.200801372.

PMID:
18956399
8.

A mass spectrometry method for the determination of enantiomeric excess in mixtures of D,L-amino acids.

Grigorean G, Ramirez J, Ahn SH, Lebrilla CB.

Anal Chem. 2000 Sep 15;72(18):4275-81.

PMID:
11008760
9.
10.
13.

Mass spectrometric quantitation of chiral drugs by the kinetic method.

Tao WA, Gozzo FC, Cooks RG.

Anal Chem. 2001 Apr 15;73(8):1692-8.

PMID:
11338581
14.

Chiral discrimination of alpha-amino acids by DNA tetranucleotides under electrospray ionization conditions.

Sivaleela T, Kumar MR, Prabhakar S, Bhaskar G, Vairamani M.

Rapid Commun Mass Spectrom. 2008;22(2):204-10.

PMID:
18088066
16.

Chiral analysis by mass spectrometry using the kinetic method in flow systems.

Lemr K, Ranc V, Frycák P, Bednár P, Sevcík J.

J Mass Spectrom. 2006 Apr;41(4):499-506.

PMID:
16541388
17.

Chiral melamine derivatives: design, synthesis, and application to mass spectrometry-based chiral analysis.

Liu Q, Zhang S, Wu B, Guo J, Xie J, Gu M, Zhao Y, Yun L, Liu K.

Anal Chem. 2005 Aug 15;77(16):5302-10.

PMID:
16097772
18.

The role of pi-acidic and pi-basic chiral stationary phases in the high-performance liquid chromatographic enantioseparation of unusual beta-amino acids.

Ilisz I, Berkecz R, Forró E, Fülöp F, Armstrong DW, Péter A.

Chirality. 2009 Mar;21(3):339-48. doi: 10.1002/chir.20542.

PMID:
18553499
20.
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