| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5291601 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Alkyl isocyanides react with 2-hydroxybenzaldehyde or 2-hydroxy-5-nitrobenzaldehyde to afford N-alkyl-2-aryl-2-oxoacetamides and N2,N4-dialkyl-2-aryl-4H-1,3-benzodioxine-2,4-dicarboxamides in nearly 1:1 ratios. Treatment of 2,6-dimethylphenyl isocyanide with 2-hydroxy-5-nitrobenzaldehyde affords only the 2-oxoacetamide derivative.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Issa Yavari, Hoorieh Djahaniani,