𝔖 Bobbio Scriptorium
✦   LIBER   ✦

13C and 15N NMR investigation of the prototropic equilibrium of 2-hydroxy-3-methylindazole

✍ Scribed by W. Schilf; L. Stefaniak; G. A. Webb


Publisher
John Wiley and Sons
Year
1987
Tongue
English
Weight
327 KB
Volume
25
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


It is shown that both I3C and ''N NMR measurements provide similar estimates of the position of the prototropic equilibrium exhibited by 2-hydroxy-3-methylindazole in three solvents. The "N NMR study of the pyridine and pyrrole types of nitrogen atoms provided the most quantitatively reliable results. The position of the prototropic equilibrium was found to be critically dependent on the acidity of the chosen solvent, the quinonoid form being predominant in weakly acidic media.


📜 SIMILAR VOLUMES


Study of the prototropic tautomerism of
✍ Gerrit L'abbé; Marie-Anne Persoons; Suzanne Toppet 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 257 KB

Comparison of the "C and "N NMR spectra of 8-azatheophylline with those of its three methylated derivatives and other model compounds from the literature showed that 8-azatheophylline exists to the extent of 80% in the N-2 tautomeric form in DMSO solution.

Theoretical and experimental 13C and 15N
✍ Tales L. C. Martins; Teodorico C. Ramalho; José D. Figueroa-Villar; Alex F.C. Fl 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 130 KB

## Abstract Experimental and theoretical ^15^N and ^13^C NMR data for the three nitrobenzaldehyde guanylhydrazones are reported. The theoretical data were obtained using sequential molecular dynamics/quantum mechanics methodology for the calculation of flexible molecules in a condensed phase, follo

Derivatives of pyrazinecarboxylic acid:
✍ Wolfgang Holzer; Gernot A. Eller; Barbara Datterl; Daniela Habicht 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 159 KB

## Abstract NMR spectroscopic studies are undertaken with derivatives of 2‐pyrazinecarboxylic acid. Complete and unambiguous assignment of chemical shifts (^1^H, ^13^C, ^15^N) and coupling constants (^1^H,^1^H; ^13^C,^1^H; ^15^N,^1^H) is achieved by combined application of various 1D and 2D NMR spe

1H, 13C and 15N NMR spectra of [1,2-15N2
✍ Alain Fruchier; Valdo Pellegrin; Rosa Maria Claramunt; Jose Elguero 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 199 KB

## REFERENCE DATA carbons, for various substituent groups and positions were carried out by gated decoupling with NOE. ## RESULTS AND DISCUSSION The I3C NMR chemical shifts of the compounds are shown in Tables 123; 'J(CH) and long-range coupling constants of 2, 9, 13 and 18, measured by gated d

The syntheses of [14C] and [13C2,15N3]ap
✍ Charles S. Elmore; Dennis C. Dean; Yong Zhang; David G. Mellilo 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 French ⚖ 133 KB

## Abstract In support of a program to develop a treatment for chemotherapy‐induced nausea and vomiting, two isotopically labeled forms of neurokinin‐1 receptor antagonist aprepitant have been synthesized. A [^l4^C]‐labeled version was synthesized for use in metabolism studies, while a [^13^C~2~,^1

13C and 15N NMR study of 2,3-diphenyltet
✍ W. Kozminski; J. Jazwinski; L. Stefaniak; G. A. Webb 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 213 KB

## Abstract ^13^C and ^15^N NMR chemical shifts are reported for 2,3‐diphenyltetrazolium‐5‐olate and ‐5‐thiolate and some of their derivatives. The data for N‐1 and C‐5 provide a very satisfactory means of distinguishing between O and S as the exocyclic substituent. The reported chemical shifts are