First example of direct introduction of nucleophiles bearing a stable radical moiety into azaaromatic substrates / Verbitskiy E. V.,Rusinov G. L.,Slepukhin P. A.,Matern A. I.,Shvachko Yu. N.,Starichenko D. V.,Charushin V. N.,Chupakhin O. N. // RUSSIAN CHEMICAL BULLETIN. - 2006. - V. 55, l. 11. - P. 2114-2116.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

Addition products of 4-hydroximino-2,2,6,6-tetramethylpiperidine-1-oxyl with 5-aryl-2,3-dicyano-1-ethylpyrazinium salts were isolated for the first time. Crystallographic data on the three-dimensional structures of sigma(H)-adducts bearing a stable radical moiety were obtained.

Author keywords:

2,3-dicyano-1-ethyl-5-phenylpyrazinium and 2,3-dicyano-1-ethyl-5-(4-fluorophenyl)pyrazinium tetrafluoroborates; 4-hydroximino-2,2,6,6-tetramethylpiperidine-1-oxyl; sigma(H)-adducts with O-nucleophiles NITROXIDE; SPECTROSCOPY; INHIBITION; TEMPOL

DOI:

10.1007/s11172-006-0558-7

Web of Science ID:

ISI:000245501600031

Соавторы в МНС:

Другие поля

Поле	Значение
Month	NOV
Publisher	SPRINGER
Address	233 SPRING STREET, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	NITROXIDE; SPECTROSCOPY; INHIBITION; TEMPOL
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	rusinov@ios.uran.ru Yurii.Shvachko@imp.uran.ru
ResearcherID-Numbers	Starichenko, Denis/J-9813-2013
ORCID-Numbers	Starichenko, Denis/0000-0001-9481-538X
Number-of-Cited-References	18
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	2
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	154IY