Autor: |
Michail N. Elinson, Evgeniya O. Dorofeeva, Gennady I. Nikishin, Tatiana A. Zaimovskaya, Nikita O. Stepanov, Anatolii N. Vereshchagin |
Rok vydání: |
2013 |
Předmět: |
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Zdroj: |
Tetrahedron. 69:1945-1952 |
ISSN: |
0040-4020 |
DOI: |
10.1016/j.tet.2012.12.029 |
Popis: |
Electrolysis of aldehydes, barbituric acids, and malononitrile in alcohol in an undivided cell in the presence of sodium bromide results in efficient MHIRC formation of the corresponding spirocyclopropylbarbiturates in 50–65% substance yield. The electrocatalytic reaction smoothly proceeds under neutral and mild conditions with aromatic aldehydes bearing both electron-donating and electron-withdrawing groups. The implication of electrocatalysis in MHIRC reaction is an efficient approach to medicinally relevant spirocyclopropylbarbiturates avoiding the inconvenient direct use of molecular halogen or halogenated substrates. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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