Cinchona alkaloid and di-tert-butyldicarbonate–DMAP promoted efficient synthesis of (E)-nitroolefins
The synthesis of nitroolefins from aldehydes and olefins is generally limited by the formation of a mixture of cis and trans compounds. Here we report an alternative, metal-free protocol for the synthesis of β-nitroolefins from arylidinemalononitrile using cinchona alkaloid along with di- tert -buty...
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Veröffentlicht in: | RSC advances 2016-01, Vol.6 (59), p.54495-54502 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The synthesis of nitroolefins from aldehydes and olefins is generally limited by the formation of a mixture of
cis
and
trans
compounds. Here we report an alternative, metal-free protocol for the synthesis of β-nitroolefins from arylidinemalononitrile using cinchona alkaloid along with di-
tert
-butyldicarbonate–DMAP in high yields with total selectivity. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C6RA06644E |