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Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 2014, Volume: 50, Number: 8, Pages: 1113-1125 Pages count : DOI: 10.1007/s10593-014-1571-7
Tags 4-hydroxycyclohexanone; 3-imidazolines; spirocyclic nitroxyl radicals; condensation; Mitsunobu acylation
Authors Zaitseva E. V. 1 , Shernyukov A. V. 1 , Amitina S. A. 1 , Tamura R. 2 , Grigor'ev I. A. 1 , Mazhukin D. G. 1,3
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Kyoto Univ, Grad Sch Human & Environm Studies, Sakyo Ku, Yoshida Nihonmatsu, Kyoto 6068501, Japan
3 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Abstract: Alkylaromatic alpha-hydroxylamino ketones with a p-hydroxy(alkoxy)aryl substituent were used for the preparation of stable diastereomeric spirocyclic nitroxyl radicals of 3-imidazoline series, having two different or identical mesogenic groups in the molecule. The molecular structure of these compounds was determined by NMR study of their diamagnetic reduced derivatives.
Cite: Zaitseva E.V. , Shernyukov A.V. , Amitina S.A. , Tamura R. , Grigor'ev I.A. , Mazhukin D.G.
Synthesis of Diastereomeric Spirocyclic Nitroxyl Radicals of 3-Imidazoline Series with Two Mesogenic Groups
Chemistry of Heterocyclic Compounds. 2014. V.50. N8. P.1113-1125. DOI: 10.1007/s10593-014-1571-7 WOS Scopus РИНЦ OpenAlex
Dates:
Published online: Oct 8, 2014
Published print: Nov 1, 2014
Identifiers:
Web of science: WOS:000344093400006
Scopus: 2-s2.0-84921937001
Elibrary: 24030915
OpenAlex: W2002277872
Citing:
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Web of science 2
Scopus 2
Elibrary 1
OpenAlex 2
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