| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278077 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Nitroethylenes possessing aryl, heteroaryl, and alkyl substituents at the β-position as well as δ-substituted nitrobutadienes undergo facile aminoalkylation at the α-position upon treatment with formaldehyde and a secondary amine in the presence of imidazole and trifluoroacetic acid to afford α-aminoalkylated nitroalkenes and nitrodienes in good to excellent yield and stereoselectivity.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kunjanpillai Rajesh, Pramod Shanbhag, Manjoji Raghavendra, Pallavi Bhardwaj, Irishi N.N. Namboothiri,