𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Selective inverse correlation of 13C and 1H NMR signals, an alternative to 2D NMR

✍ Scribed by Stefan Berger

Publisher
Elsevier Science
Year
1989
Weight
208 KB
Volume
81
Category
Article
ISSN
0022-2364

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Revised Assignments of the 13C NMR Spect
Revised Assignments of the 13C NMR Spectra of Grossularine-1 and -2 Using 2D Heteronuclear 1H–13C Correlations
✍ Ali Loukaci; MichΓ¨le Guyot πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 198 KB πŸ‘ 2 views

## One-bond and long-range two-dimensional 'H-I'C NMR experiments allow the unequivocal assignment of 13C and 'H spectra. On this basis, previous assignments of 13C signals of grossularine-1 and -2 have been revised.

Complete 1H and 13C assignments of racto
Complete 1H and 13C assignments of ractopamine hydrochloride using 2D and selective 1D NMR methods
✍ J. K. Huwe; S. Castellino; D. J. Smith πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 295 KB

## Abstract The ^1^H and ^13^C NMR resonances for ractopamine hydrochloride have been assigned. H,H‐COSY and H,C‐COSY were used to assign the aliphatic moiety of the molecule and to correlate protons and carbons on the same ring system. Long‐range selective proton decoupling (LSPD) experiments were

Application of 1H/13C inversely correlat
Application of 1H/13C inversely correlated NMR spectroscopy to the determination of the stereochemistry of a polysubstituted [2.2]paracyclophane
✍ RΓΌdiger E. Fischer; Janusz Dabrowski; Andrzej Ejchart; Heinz A. Staab πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 409 KB

The relative orientation of substituents in the opposite rings of one of the isomeric 4,7-dichloro-5,8,12,19 tetramethoxy-13,1Cbis[~~methoxycarbonylphenyl)butyl~[2.2~paracyclophanes was determined by establishing by NOE their orientation relative to the bridge protons, which thus served as 'space-sp