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Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide. / Zenkevich, I.G.; Pushkareva, T.I.

In: Russian Journal of General Chemistry, Vol. 85, No. 8, 2015, p. 1920-1928.

Research output: Contribution to journal › Article › peer-review

Harvard

Zenkevich, IG & Pushkareva, TI 2015, 'Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide', Russian Journal of General Chemistry, vol. 85, no. 8, pp. 1920-1928. https://doi.org/10.1134/S1070363215080204

APA

Zenkevich, I. G., & Pushkareva, T. I. (2015). Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide. Russian Journal of General Chemistry, 85(8), 1920-1928. https://doi.org/10.1134/S1070363215080204

Vancouver

Zenkevich IG, Pushkareva TI. Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide. Russian Journal of General Chemistry. 2015;85(8):1920-1928. https://doi.org/10.1134/S1070363215080204

Author

Zenkevich, I.G. ; Pushkareva, T.I. / Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide. In: Russian Journal of General Chemistry. 2015 ; Vol. 85, No. 8. pp. 1920-1928.

BibTeX

@article{784c3a6bcb7f42be9c67ae72b9d7b34c,
title = "Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide",
abstract = "{\textcopyright} 2015 Pleiades Publishing, Ltd.A series of amino acids have been converted into the derivatives via interaction with dimethylformamide dimethyl acetal for gas chromatography identification. The derivatives have been for the first time characterized with mass spectra and retention indices corresponding to the standard nonpolar polydimethylsiloxane stationary phases. Basic features of mass spectroscopic fragmentation of the derivatives have been stated; the rules for interpretation of their gas chromatography retention indices have been figured out, including the additive scheme elements.",
author = "I.G. Zenkevich and T.I. Pushkareva",
year = "2015",
doi = "10.1134/S1070363215080204",
language = "English",
volume = "85",
pages = "1920--1928",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "8",

}

RIS

TY - JOUR

T1 - Chromatographic and chromato-mass spectral characterization of amino acids derivatives formed via the interaction with dimethyl acetal of dimethylformamide

AU - Zenkevich, I.G.

AU - Pushkareva, T.I.

PY - 2015

Y1 - 2015

N2 - © 2015 Pleiades Publishing, Ltd.A series of amino acids have been converted into the derivatives via interaction with dimethylformamide dimethyl acetal for gas chromatography identification. The derivatives have been for the first time characterized with mass spectra and retention indices corresponding to the standard nonpolar polydimethylsiloxane stationary phases. Basic features of mass spectroscopic fragmentation of the derivatives have been stated; the rules for interpretation of their gas chromatography retention indices have been figured out, including the additive scheme elements.

AB - © 2015 Pleiades Publishing, Ltd.A series of amino acids have been converted into the derivatives via interaction with dimethylformamide dimethyl acetal for gas chromatography identification. The derivatives have been for the first time characterized with mass spectra and retention indices corresponding to the standard nonpolar polydimethylsiloxane stationary phases. Basic features of mass spectroscopic fragmentation of the derivatives have been stated; the rules for interpretation of their gas chromatography retention indices have been figured out, including the additive scheme elements.

U2 - 10.1134/S1070363215080204

DO - 10.1134/S1070363215080204

M3 - Article

VL - 85

SP - 1920

EP - 1928

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 8

ER -

ID: 4003728