Stereochemical features of addition of O- and C-nucleophiles to 5-(Het)aryl-2,3-dicyano-1-ethylpyrazinium salts / Verbitskii E. V.,Rusinov G. L.,Slepukhin P. A.,Grishakov A. N.,Ezhikova M. A.,Kodess M. I.,Charushin V. N. // RUSSIAN JOURNAL OF ORGANIC CHEMISTRY. - 2008. - V. 44, l. 2. - P. 302-310.

ISSN/EISSN:

1070-4280 / нет данных

Type:

Article

Abstract:

Stable sigma(H)-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 I 2-dihydropyrazines into individual enantiomers by means of HPLC on columns with chiral sorbents.

Author keywords:

PHOTODYNAMIC ACTIVITY; AMINES; WATER; AZAPHTHALOCYANINES; ALCOHOLS; ADDUCTS; CATIONS

DOI:

10.1134/S107042800802019X

Web of Science ID:

ISI:000254140900019

Соавторы в МНС:

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Другие поля

Поле	Значение
Month	FEB
Publisher	MAIK NAUKA/INTERPERIODICA/SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013-1578 USA
Language	English
Keywords-Plus	PHOTODYNAMIC ACTIVITY; AMINES; WATER; AZAPHTHALOCYANINES; ALCOHOLS; ADDUCTS; CATIONS
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	rusinov@ios.uran.ru
Number-of-Cited-References	21
Usage-Count-Since-2013	1
Journal-ISO	Russ. J. Organ. Chem.
Doc-Delivery-Number	276KU