Pyridine-Functionalized C4 Symmetric Resorcinarenes.
β Scribed by Matthew J. McIldowie; Mauro Mocerino; Mark I. Ogden; Biran W. Skelton
- Book ID
- 102015348
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 11 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Novel substituted thiazole[4,5-c]pyridines have been synthesized in good yields from unsubstituted thiazole[4,5-c]pyridine using direct C-H coupling reactions and N-oxide rearrangement chemistry.
Four different 4-functionalised pyridine-based ligands were synthesized with aminomethyl, oxazolinyl, pyrazolyl and methylimidazolyl groups at the 2-and 6-position. The nitrogens of these groups together with the pyridine nitrogen can act as terdendate ligands for metal ions. Synthetic handles on th
The facile introduction of nucleophiles in the 4 position 2b and the possibilities of photorearrangement, render the isoxazolo[4,5-c]pyridine of valuable interest in the synthetic approach to a number of pyridine condensed heterocycles. Acknowledpment.