NMR studies on derivatives of heteroaromatic compounds: exceptionally small carbon-carbon couplings, 1J(CC), in 2-lithiothiophene, 2-lithio-N-methylpyrrole and 2-lithiofuran.

@article{Dbrowski2000NMRSO,
  title={NMR studies on derivatives of heteroaromatic compounds: exceptionally small carbon-carbon couplings, 1J(CC), in 2-lithiothiophene, 2-lithio-N-methylpyrrole and 2-lithiofuran.},
  author={A. Dąbrowski and Krystyna Kamieńska‐Trela and Jacek W{\'o}jcik},
  journal={Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy},
  year={2000},
  volume={56A 1},
  pages={
          91-102
        }
}
8 Citations
Substituent effects on indirect carbon–carbon couplings, J(CC), in substituted thiophenes, pyrroles, and furans studied by experiment and theory
An excellent linear correlation is found between a large set of experimental spin–spin carbon–carbon coupling constants, J(CC), in thiophene, pyrrole, and furan systems and the corresponding
NMR Scalar Couplings and Molecular Interactions
In this work, a description is given of the possibilities that, at present, can be envisioned for using NMR scalar spin–spin couplings for studying molecular systems. Such possibilities are based

References

SHOWING 1-10 OF 32 REFERENCES
Nuclear Magnetic Resonance Spectroscopy. Carbon-13 Spectra of Five-Membered Aromatic Heterocycles
High-resolution ^(13)C nmr spectra have been obtained for the five-membered nitrogen heterocycles and for furan, thiophene, and selenophene. All possible carbon-proton coupling constants have been
Spin—spin couplings between 13C nuclei in five‐membered heteroaromatic ring systems
A set of 14 1J(CC) spin—spin coupling constants are reported for 11 five‐membered heteroaromatic molecules, including all relevant diazole, triazole, oxazole, oxadiazole, thiazole and thiadiazole
Preparative polar organometallic chemistry
I. Reactivity of Polar Organometallic Intermediates.- 1 Introduction.- 2 Alkylation.- 2.1 Reactivity-A Qualitative Comparison of the Polar Organometallics.- 2.2 Scope of the Alkylation Reaction.- 2.3
...
...