Synthesis of diastereomeric spirocyclic nitroxyl radicals of 3-imidazoline series with two mesogenic groups
Chemistry of Heterocyclic Compounds, ISSN: 1573-8353, Vol: 50, Issue: 8, Page: 1113-1125
2014
- 2Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
Alkylaromatic α-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.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84921937001&origin=inward; http://dx.doi.org/10.1007/s10593-014-1571-7; http://link.springer.com/10.1007/s10593-014-1571-7; http://link.springer.com/content/pdf/10.1007/s10593-014-1571-7; http://link.springer.com/content/pdf/10.1007/s10593-014-1571-7.pdf; http://link.springer.com/article/10.1007/s10593-014-1571-7/fulltext.html; https://dx.doi.org/10.1007/s10593-014-1571-7; https://link.springer.com/article/10.1007/s10593-014-1571-7
Springer Science and Business Media LLC
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