𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis,1H,13C,14N, and15N NMR spectra, and cathodic behavior of N-chloro-1,2,4-triazoles

✍ Scribed by V. V. Kozlov; M. E. Niyazymbetov; M. S. Pevzner; B. I. Ugrak; V. A. Petrosyan

Book ID
112494412
Publisher
Springer
Year
1990
Tongue
English
Weight
548 KB
Volume
39
Category
Article
ISSN
1573-9171

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1H, 13C and 15N NMR spectra of [1,2-15N2
1H, 13C and 15N NMR spectra of [1,2-15N2]pyrazole derivatives
✍ 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

1H, 13C and 15N NMR spectra of ciproflox
1H, 13C and 15N NMR spectra of ciprofloxacin
✍ Andrzej Ziȩba; Andrzej Maślankiewicz; Jerzy Sitkowski 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 103 KB

## Abstract ^1^H NMR assignment, including the values of δ~H~ and __J__(H,H) for the cyclopropane moiety, and ^13^C NMR and ^15^N NMR spectral data for ciprofloxacin are presented. Copyright © 2004 John Wiley & Sons, Ltd.

Synthesis of tetrazole-13C and 1,2,4-tri
Synthesis of tetrazole-13C and 1,2,4-triazole-1,2-15N2
✍ Roger S. Rowlett; Thomas Klysa; William W. Shiraki 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 French ⚖ 141 KB

## Abstract We report here the syntheses of tetrazole‐^13^C and 1,2,4‐triazole‐1,2‐^15^N~2~ by simple, one‐step procedures using common, commercially available, isotopically‐labeled starting materials. tetrazole‐ ^13^C is conveniently prepared from K^13^CN and NaN~3~ in 70% yield, almost twice the

1H, 13C and 15N NMR study of N1-alkyl-N2
1H, 13C and 15N NMR study of N1-alkyl-N2-arylthioureas
✍ Iwona Wawer; Vera Koleva 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 407 KB

## Abstract ^13^C and ^15^N NMR chemical shifts were measured for __N__^1^‐alkyl‐__N__^2^‐arylthioureas. The absence of decoalescence of the __N__^1^‐alkyl group carbon signals down to 190 K, the europium‐induced chemical shifts and the molecular mechanics calculations indicate that the preferred c