Abstract
Substituted naphthyridines containing isoquinolinic nitrogen were synthesized by the reaction of o-ethynylpyridinecarbaldehydes with ammonia. The synthesis of their N-oxides was also achieved by a basic cyclization reaction of the same pyridine derivatives via the corresponding oximes.
| Original language | English |
|---|---|
| Pages (from-to) | 306-311 |
| Number of pages | 6 |
| Journal | Synthesis |
| Issue number | 2 |
| Publication status | Published - 1999 Jan 1 |
Keywords
- Cyclization
- Lithiation
- N-oxides
- Naphthyridines
- Palladium-catalyzed acetylene cross- coupling
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry
Fingerprint Dive into the research topics of 'General synthetic method for naphthyridines and their N-oxides containing isoquinolinic nitrogen'. Together they form a unique fingerprint.
Cite this
Numata, A., Kondo, Y., & Sakamoto, T. (1999). General synthetic method for naphthyridines and their N-oxides containing isoquinolinic nitrogen. Synthesis, (2), 306-311.