## Abstract The synthesis and complete assignment of all hydrogen, carbon and nitrogen NMR signals of several new isoxazolo[3,4‐__d__]pyridazin‐7(6__H__)‐ones is reported. The spectroscopic characterization is extended to previously described analogues. Copyright © 2004 John Wiley & Sons, Ltd.
Synthesis and complete assignment of the 1H and 13C NMR spectra of 6-substituted and 2,6-disubstituted pyridazin-3(2H)-ones
✍ Scribed by Pedro Besada; Tamara Costas; Noemi Vila; Carla Chessa; Carmen Terán
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 116 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2755
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✦ Synopsis
Abstract
Several pyridazin‐3(2__H__)‐one derivatives were synthesized starting from alkyl furans using oxidation with singlet oxygen to give 4‐methoxy or 4‐hydroxybutenolides, key intermediates of the synthetic strategy followed. For all pyridazinones reported, a complete assignment of the ^1^H and ^13^C NMR spectra using one‐ and two‐dimensional NMR spectroscopic methods, which included NOE, DEPT, COSY, HSQC and HMBC experiments, was accomplished. Correlations between the chemical shifts of the heterocyclic ring atoms and substituents at N‐2 and C‐6 were analyzed. Copyright © 2011 John Wiley & Sons, Ltd.
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