Complete 1H and 13C NMR chemical shift assignment of N1- and N3-alkylnitrohistidines and of 1,4,6,7-tetrahydroimidazo[4,5-b]pyridines
✍ Scribed by Carmen Escolano; Marcelo J. Kogan; Mario Rubiralta; Ernest Giralt; Anna Diez
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 93 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1156
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^1^H and ^13^C NMR data for 13 nitrohistidine derivatives are reported, providing a diagnostic method for the elucidation of the N^1^‐(2) and the N^3^‐substituted (3) regioisomers. Spectral assignments of constrained surrogates of His (4) and of the His–Gly dipeptide (5 and 6) are also described. The structure of the compounds was confirmed by NOESY and heteronuclear (^13^C, ^1^H) short‐ and long‐range correlation experiments. Copyright © 2003 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract ^1^H, ^13^C and ^15^N NMR measurements (1D and 2D including ^1^H^15^N gs‐HMBC) have been carried out on 3‐amino‐1, 2,4‐benzotriazine and a series of __N__‐oxides and complete assignments established. __N__‐Oxidation at any position resulted in large upfield shifts of the corresponding
## Abstract The assignment of the signals in the ^13^C and ^1^H NMR spectra of __N__‐phenyl‐2,4‐dimethylbuta‐1,3‐diene‐1,4‐sultam is difficult for the signal pairs C‐2 and C‐4, C‐1 and C‐3, (C‐1)H, (C‐2)CH~3~ and (C‐4)CH~3~. The ^13^C NMR spectrum recorded under gated decoupling conditions provi
## 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.
The 1H and 13C NMR resonances of four 3H-naphtho[2,1-b]pyrans were completely and unambiguously assigned by a combination of homonuclear (gs-COSY), 1H-detected heteronuclear one-bond (gs-HMQC) and long-range (gs-HMBC) gradient-selected correlation experiments.
## Abstract ^1^H, ^13^C and ^15^N NMR chemical shifts of 10 substituted pyrazolo[1,5‐__a__]pyrimidines were assigned based on DQF ^1^H, ^1^H COSY, PFG ^1^H, ^13^C HMQC and PFG ^1^H,X (X = ^13^C and ^15^N) HMBC experiments and on literature data. Copyright © 2002 John Wiley & Sons, Ltd.