Synthesis of Amides by Nucleophilic Substitution of Hydrogen in 3-Nitropyridine
3-Nitropyridine reacted with nitrogen-centered carboxylic acid amide anions in anhydrous DMSO in the presence of K3Fe(CN)6 via oxidative nucleophilic substitution of hydrogen to give previously unknown N-(5-nitropyridin-2-yl) carboxamides. The reaction of nitrobenzene with urea anion in DMSO enabled...
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| Huvudupphovsmän: | , , , , , , , , , |
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| Materialtyp: | Статья |
| Språk: | English |
| Publicerad: |
Pleiades Publishing
2018
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| Ämnen: | |
| Länkar: | https://www.scopus.com/record/display.uri?eid=2-s2.0-85050465848&origin=resultslist&sort=plf-f&src=s&nlo=&nlr=&nls=&sid=5f9b6becf5270e68a8c48a2159c718f9&sot=aff&sdt=sisr&sl=145&s=AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29+OR+AF-ID%28%22%5bNo+Affiliation+ID+found%5d%22+60070961%29+OR+AF-ID%28%22%5bNo+Affiliation+ID+found%5d%22+60026323%29&ref=%28Synthesis+of+Amides+by+Nucleophilic+Substitution+of+Hydrogen+in+3-Nitropyridine%29&relpos=0&citeCnt=0&searchTerm= https://dspace.ncfu.ru/handle/20.500.12258/2806 |
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| Sammanfattning: | 3-Nitropyridine reacted with nitrogen-centered carboxylic acid amide anions in anhydrous DMSO in the presence of K3Fe(CN)6 via oxidative nucleophilic substitution of hydrogen to give previously unknown N-(5-nitropyridin-2-yl) carboxamides. The reaction of nitrobenzene with urea anion in DMSO enabled one-pot synthesis of bis(4-nitrophenyl)amine |
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