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NMR studies in the heterocyclic series. XXXII. Carbon-13 NMR study of N-arylpyrazoles and N-arylpyrazolium salts

✍ Scribed by Antonio De La Hoz; Maria Del Carmen Pardo; José Elguero; Alain Fruchier


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
253 KB
Volume
27
Category
Article
ISSN
0749-1581

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✦ Synopsis


A comparative study of the 13C chemical shifts and the 'H-13C and 19F-13C coupling constants of N-arylpyrazoles, pyrazolium salts and 2-methyl-and 2-vinylpyrazolium quaternary salts has been carried out. The effect of introducing a substituent at positions 2 and 5 of the pyrazole ring on the conjugation between the heterocycle and the N-phenyl group has been studied.

KEY WORDS "C NMR

Chemical shifts J(CH) and J(FC) N-Arylpyrazoles N -Arylpyrazolium salts ' H-'H and ' H-' 3C COSY experiments, and permit an evaluation of linear vs. angular endo and ex0 ketone orientation on the NMR parameters.

KEY WORDS "C NMR 'H N M R Tricyclic aromatic ketones

Linear and angular effects


📜 SIMILAR VOLUMES


NMR studies in the heterocyclic series.
✍ Alain Fruchier; José Elguero; Anthony F. Hegarty; Daniel G. McCarthy 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 314 KB

## Abstract Assignment of the carbon resonances in nine derivatives of __N__‐hydroxybenzotriazole has been carried out. The ^13^C NMR method enables tautomeric __N__‐hydroxy and __N__‐oxide and isomeric __O__‐ and __N__‐acyl structures to be identified. In DMSO, the predominant tautomer of __N__‐hy

NMR studies in the heterocyclic series.
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## Abstract The carbon‐13 chemical shifts and the ^1^__J__(CH) coupling constants for 18 azolium salts (di‐__N__‐methyl‐pyrazolium, ‐indazolium, ‐benzimidazolium and ‐benzotriazolium iodides) have been determined and assigned. The chemical shifts are discussed as a function of substituent effects,

NMR studies in the heterocyclic series X
✍ Alain Fruchier; Valdo Pellegrin; Rémy Schimpf; José Elguero 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 352 KB

## Abstract The ^15^N chemical shifts and ^1^H^15^N and ^13^C^15^N coupling constants of nine monolabelled indazoles were measured and assigned. The experimental values are discussed in terms of the indazolic and iso‐indazolic structures, and compared with literature data for other related hetero