Abstract
As the third step of a new general synthesis of pyrido[2,3‐d]pyrimidines, the substitution of the halogens by several nucleophiles has been carried out. Yields are between good and high in every case, even when 4‐halogenated compounds have a neighbouring methyl group in C5.
| Original language | English |
|---|---|
| Pages (from-to) | 245-247 |
| Number of pages | 3 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 25 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 1988 |
| Externally published | Yes |
Fingerprint
Dive into the research topics of 'New synthesis of pyrido[2,3‐d]pyrimidines. III. Nucleophilic substitution on 4‐amino‐2‐halo and 2‐amino‐4‐halo‐5,6‐dihydropyrido[2,3‐d]pyrimidin‐7(8H)‐ones'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver