Research output: Contribution to journal › Article › peer-review
The interaction of the ethyl ester or pyrrolidide of 3, 3-diaminoacrylic acid with aromatic and heteroaromatic nitriles containing a labile halogen atom in the ortho position, leads to the formation of products of its substitution by the α-carbon atom of the diaminoacrylic acid derivative. The compounds obtained are cyclized smoothly into fused diaminoazines.
| Original language | English |
|---|---|
| Pages (from-to) | 436-441 |
| Number of pages | 6 |
| Journal | Chemistry of Heterocyclic Compounds |
| Volume | 48 |
| Issue number | 3 |
| DOIs | |
| State | Published - 2012 |
ID: 5482048