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Donor-acceptor pyran-2-ones: Absorption and fluorescence spectra of 4-substituted 2H-1-benzo/napthopyran-2-ones
✍ Scribed by Rajesh S. Kenny; Uday C. Mashelkar
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2006
- Tongue
- English
- Weight
- 70 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
The absorption spectra and emission spectra of 4-substituted 2H-1-benzo/napthopyran-2-ones 3a-l have been determined in THF and DMSO. The substituent at the 4-position of the 2H-benzo/napthopyran-2-one, establishes a compact conjugation pathway in which the pyran-2-one nucleus can act as an acceptor ring.
📜 SIMILAR VOLUMES
New Mass Spectra Substituted Pyrimidojl.2-b]pyridazin-2(2H)-oaes and Isomeric 4(4H)-ones; Scope and Limitations of a Diagnostic Fragmentation Reaction \* Molecular ion: percentage of total ion current. \*\* Fragment ions: percentage of total fragment ion current, i.e. cy-1 I(rn/z).
## Abstract We report the condensation of substituted 2‐aminopyridines 5 with β‐ketocarboxylic esters in polyphosphoric acid. In this reaction were obtained together with the target compounds, 4__H__‐pyrido[1,2‐__a__]pyrirnidin‐4‐ones 6 also the pyridin‐2‐ones 7. All the compounds 7 were tested for