117 related articles for article (PubMed ID: 38782584)
1.
Kleinpeter E; Koch A
Magn Reson Chem; 2024 May; ():. PubMed ID: 38782584
[TBL] [Abstract][Full Text] [Related]
2. Identification and quantification of local antiaromaticity in polycyclic aromatic hydrocarbons (PAHs) based on the magnetic criterion.
Kleinpeter E; Koch A
Org Biomol Chem; 2024 Apr; 22(15):3035-3044. PubMed ID: 38534070
[TBL] [Abstract][Full Text] [Related]
3. Antiaromaticity proved by the anisotropic effect in 1H NMR spectra.
Kleinpeter E; Koch A
J Phys Chem A; 2012 Jun; 116(23):5674-80. PubMed ID: 22512817
[TBL] [Abstract][Full Text] [Related]
4. Carbones (-C
Kleinpeter E; Koch A
Org Biomol Chem; 2024 Feb; 22(9):1907-1914. PubMed ID: 38353143
[TBL] [Abstract][Full Text] [Related]
5. Quantification of σ-Acceptor and π-Donor Stabilization in
Kleinpeter E; Koch A
J Phys Chem A; 2021 Aug; 125(33):7235-7245. PubMed ID: 34387991
[TBL] [Abstract][Full Text] [Related]
6. Identification of benzenoid and quinonoid structures by through-space NMR shieldings (TSNMRS).
Kleinpeter E; Koch A
J Phys Chem A; 2010 May; 114(18):5928-31. PubMed ID: 20377212
[TBL] [Abstract][Full Text] [Related]
7. Carbones - A Classification on the Magnetic Criterion.
Kleinpeter E; Koch A
Chem Asian J; 2024 Jan; 19(2):e202300826. PubMed ID: 37966046
[TBL] [Abstract][Full Text] [Related]
8. Quantification of the aromaticity of 2-alkylidenethiazolines subjected to push-pull activity.
Baranac-Stojanović M; Kleinpeter E
J Org Chem; 2011 May; 76(10):3861-71. PubMed ID: 21463000
[TBL] [Abstract][Full Text] [Related]
9. Anisotropy effect of three-membered rings in (1)H NMR spectra: quantification by TSNMRS and assignment of the stereochemistry.
Kleinpeter E; Krüger S; Koch A
J Phys Chem A; 2015 May; 119(18):4268-76. PubMed ID: 25860405
[TBL] [Abstract][Full Text] [Related]
10. Endohedral and external through-space shieldings of the fullerenes c50, c60, c60(-6), c70, and c70(-6)-visualization of (anti)aromaticity and their effects on the chemical shifts of encapsulated nuclei.
Kleinpeter E; Klod S; Koch A
J Org Chem; 2008 Feb; 73(4):1498-507. PubMed ID: 18197684
[TBL] [Abstract][Full Text] [Related]
11. Chelatoaromaticity--existing: yes or no? An answer given by spatial magnetic properties (through space NMR shieldings--TSNMRS).
Kleinpeter E; Koch A
Phys Chem Chem Phys; 2011 Dec; 13(46):20593-601. PubMed ID: 21879066
[TBL] [Abstract][Full Text] [Related]
12. Subtle trade-off existing between (anti)aromaticity, push-pull interaction, keto-enol tautomerism, and steric hindrance when defining the electronic properties of conjugated structures.
Kleinpeter E; Bölke U; Koch A
J Phys Chem A; 2010 Jul; 114(28):7616-23. PubMed ID: 20586465
[TBL] [Abstract][Full Text] [Related]
13. Infinitene as two fused helicoidal trails of fused rings: evaluation of the magnetic behavior of [12]infinitene and anionic species displaying global aromaticity and antiaromaticity.
Olea Ulloa C; Muñoz-Castro A
Phys Chem Chem Phys; 2023 Mar; 25(11):8190-8197. PubMed ID: 36880673
[TBL] [Abstract][Full Text] [Related]
14. Push-pull vs captodative aromaticity.
Shainyan BA; Fettke A; Kleinpeter E
J Phys Chem A; 2008 Oct; 112(43):10895-903. PubMed ID: 18834089
[TBL] [Abstract][Full Text] [Related]
15. Non-intersecting ring currents in [12]infinitene.
Orozco-Ic M; Valiev RR; Sundholm D
Phys Chem Chem Phys; 2022 Mar; 24(11):6404-6409. PubMed ID: 35262148
[TBL] [Abstract][Full Text] [Related]
16. Benzenium Ion: Aromatic as the π-Complex or Antiaromatic as the σ-Complex Being Somewhat Similar to the Cyclopentadienyl Cation.
Kleinpeter E; Koch A
J Phys Chem A; 2019 May; 123(20):4443-4451. PubMed ID: 31050429
[TBL] [Abstract][Full Text] [Related]
17. Method and basis set dependence of the NICS indexes of aromaticity for benzene.
Gajda Ł; Kupka T; Broda MA; Leszczyńska M; Ejsmont K
Magn Reson Chem; 2018 Apr; 56(4):265-275. PubMed ID: 29211311
[TBL] [Abstract][Full Text] [Related]
18. Computed NMR shielding increments over benzo-analogs of unsaturated five-membered ring heterocyclic compounds as a measure of aromaticity.
Martin NH; Rowe JE; Pittman EL
J Mol Graph Model; 2010 Apr; 28(7):650-6. PubMed ID: 20129806
[TBL] [Abstract][Full Text] [Related]
19. Analysis of the origin of through-space proton NMR deshielding by selected organic functional groups.
Martin NH; Brown JD; Nance KH; Schaefer HF; Schleyer PR; Wang ZX; Woodcock HL
Org Lett; 2001 Nov; 3(24):3823-6. PubMed ID: 11720545
[TBL] [Abstract][Full Text] [Related]
20. Is the conventional interpretation of the anisotropic effects of C=C double bonds and aromatic rings in NMR spectra in terms of the π-electron shielding/deshielding contributions correct?
Baranac-Stojanović M; Koch A; Kleinpeter E
Chemistry; 2012 Jan; 18(1):370-6. PubMed ID: 22135110
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]