Stereochemical features of addition of O- and C-nucleophiles to 5-(Het)aryl-2,3-dicyano-1-ethylpyrazinium salts

Stereochemical features of addition of O- and C-nucleophiles to 5-(Het)aryl-2,3-dicyano-1-ethylpyrazinium salts

Stable σH-adducts of O- and C-nucleophiles were obtained with cations of 5-(het)aryl-2,3-dicyano-1-ethylpyrazinium, and their structure was investigated by X-ray diffraction analysis. Analytical separation was performed of 1,2-dihydropyrazines into individual enantiomers by means of HPLC on columns...

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Veröffentlicht in:Russian journal of organic chemistry 2008, Vol.44 (2), p.302-310
Hauptverfasser: Verbitskii, E. V, Rusinov, G. L, Slepukhin, P. A, Grishakov, A. N, Ezhikova, M. A, Kodess, M. I, Charushin, V. N
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Chemistry and Materials Science
Organic Chemistry
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container_issue 2
container_start_page 302
container_title Russian journal of organic chemistry
container_volume 44
creator Verbitskii, E. V
Rusinov, G. L
Slepukhin, P. A
Grishakov, A. N
Ezhikova, M. A
Kodess, M. I
Charushin, V. N
description Stable σH-adducts of O- and C-nucleophiles were obtained with cations of 5-(het)aryl-2,3-dicyano-1-ethylpyrazinium, and their structure was investigated by X-ray diffraction analysis. Analytical separation was performed of 1,2-dihydropyrazines into individual enantiomers by means of HPLC on columns with chiral sorbents.
doi_str_mv 10.1134/S107042800802019X
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Organic Chemistry
title Stereochemical features of addition of O- and C-nucleophiles to 5-(Het)aryl-2,3-dicyano-1-ethylpyrazinium salts
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