4-(Azulen-1-yl) six-membered heteroaromatics substituted with thiophen-2-yl or furan-2-yl moieties in 2 and 6 positions
✍ Scribed by Alexandru C. Razus; Liviu Birzan; Mihaela Cristea; Victorita Tecuceanu; Anamaria Hanganu; Cristian Enache
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 226 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.684
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✦ Synopsis
Abstract
Pyranylium perchlorates with azulen‐1‐yl moiety in 4‐position and thiophen‐2‐yl or furan‐2‐yl in 2 and 6‐positions were obtained by the substitution of 4‐chloro corresponding salts with azulenes. The pyranylium salts are used as starting materials for the synthesis of pyridine and pyridinium salts. The products were characterized and for pyridines pKa was spectroscopically determined. Several attempts were made for pyridine complexation with metal cations as Hg^2+^ or Ag^+^. J. Heterocyclic Chem., (2011).
📜 SIMILAR VOLUMES
## Abstract magnified image 2‐(Azulen‐1‐yl)‐4,6‐diphenyl substituted pyranylium salts, pyridinium salts and pyridines were efficiently synthesized and the new obtained compounds were completely characterized. Comparative structural analysis between these compounds and their corresponding isomers t
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v