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New Way of Direct Nitrogen Atom Phenylation in Quinoline Derivatives
Comparison of ion-molecular reactions of free-phenyl cations generated by tritium β-decay with 2-methyl- and 2-phenylquinolines has been investigated. The reaction of direct nitrogen atom phenylation with the help of nucleogenic phenyl cations has been fulfilled for the first time and a new one-step...
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Published in: | ISRN Organic Chemistry 2012-07, Vol.2012, p.1-4 |
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container_title | ISRN Organic Chemistry |
container_volume | 2012 |
creator | Shchepina, Nadezhda E. Avrorin, Viktor V. Badun, Gennady A. Lewis, Scott B. Shurov, Sergey N. |
description | Comparison of ion-molecular reactions of free-phenyl cations generated by tritium β-decay with 2-methyl- and 2-phenylquinolines has been investigated. The reaction of direct nitrogen atom phenylation with the help of nucleogenic phenyl cations has been fulfilled for the first time and a new one-step synthesis of tritium-labeled N-phenyl-2-phenylquinolinium salt—lipophilic radioactive biological marker has been elaborated. |
doi_str_mv | 10.5402/2012/526867 |
format | article |
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The reaction of direct nitrogen atom phenylation with the help of nucleogenic phenyl cations has been fulfilled for the first time and a new one-step synthesis of tritium-labeled N-phenyl-2-phenylquinolinium salt—lipophilic radioactive biological marker has been elaborated.</abstract><pub>International Scholarly Research Network</pub><pmid>24052846</pmid><doi>10.5402/2012/526867</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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title | New Way of Direct Nitrogen Atom Phenylation in Quinoline Derivatives |
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