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 |
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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 | ||||||
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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
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
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 |