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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

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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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