New possibilities of the Mannich reaction in the synthesis of N-, S,N-, and Se,N-heterocycles
The review summarizes the results obtained by our research group over the past 15 years in chemistry of N-, S,N-, and Se,N-heterocycles resulted from aminomethlation of a wide range of acyclic and heterocyclic substrates derived from active methylene amides, thioamides, and selenoamides. A series of...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Статья |
| Hizkuntza: | English |
| Argitaratua: |
SPRINGER
2019
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| Gaiak: | |
| Sarrera elektronikoa: | http://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=38&SID=E1BmcFx8KXF5GsBSl3h&page=1&doc=1 https://dspace.ncfu.ru/handle/20.500.12258/5561 |
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| Gaia: | The review summarizes the results obtained by our research group over the past 15 years in chemistry of N-, S,N-, and Se,N-heterocycles resulted from aminomethlation of a wide range of acyclic and heterocyclic substrates derived from active methylene amides, thioamides, and selenoamides. A series of 1,3,5-thia(selena)diazines, 3,7-diazabicyclo[3.3.1] nonanes, 3,5,7,11-tetraazatricyclo[7.3.1.0(2,7)]tridec-2-enes, 1,3,5,7-tetrazocines, and pyrido[1,2-a][1,3,5]triazines were synthesized. The general regularities of the Mannich reaction in the series of N-, S,N-, and Se,N-containing pyridine substrates were discussed. Biological activities of some synthesized compounds were studied to reveal compounds with antiviral, analeptic, anti-inflammatory, and antipyretic activities |
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