Collect. Czech. Chem. Commun.
1980, 45, 1575-1580
https://doi.org/10.1135/cccc19801575
13C-NMR spectra of benzenesulphonyl derivatives
Jaroslav Horyna, Antonín Lyčka and Dobroslav Šnobl
Research Institute of Organic Syntheses, 532 18 Pardubice-Rybitví
Crossref Cited-by Linking
- Resendes Barbosa Igor, Alves Amorim Mayara, de Souza Oliveira Vitor Hélio, André Eunice, Pereira Guedes Guilherme, Augusto Chaves Otávio, Serpa Carlos, Fintelman‐Rodrigues Natalia, Sacramento Carolina Q., Moreno L. Souza Thiago, Sant'Anna Carlos Mauricio R., Echevarria Aurea: Novel Sulfonamide‐Sydnone Hybrids: Complementary Insight into Anti‐Inflammatory Action, Anti‐SARS‐CoV‐2 Activity, Human Serum Albumin Interaction, and in silico Analysis. ChemMedChem 2025. <https://doi.org/10.1002/cmdc.202400697>
- Garanin Evgeny M., Tolmachev Yuriy V., Hoover Robert R., Adas Sonya, Bunge Scott D., Gangoda Mahinda, Khitrin Anatoly K., Woods Stephan M., Malkovskiy Andrey, Solak Nulifer, Wesdemiotis Chrys: Stability and Ring-Shift Tautomerization of Cyclic Anhydrides of Benzenehexasulfonic Acid. J. Org. Chem. 2010, 75, 4860. <https://doi.org/10.1021/jo1005526>
- Sonpatki Milind M, Skaria Sunny, Fradet Alain, Ponrathnam Surendra, Rajan C.R: Synthesis and structural study of poly(thioether-imide-sulfones) based on 3,3′- and 4,4′-bis(4-chloro-1,8-naphthalimido) diphenylsulfone. Polymer 1999, 40, 4377. <https://doi.org/10.1016/S0032-3861(98)00669-7>
- Brehme Rainer, Radeglia Reiner, Gründemann Egon: Aza‐Enamine. IX. UV/VIS‐ und NMR‐spektroskopische Interpretation der Elektronenstruktur in Aldehydhydrazonen und daraus hergestellten Aza‐Trimethinen. J. Prakt. Chem. 1990, 332, 911. <https://doi.org/10.1002/prac.19903320609>
- Fedorov L. A., Lycka A., Jirman J.: Multinuclear and two-dimensional NMR spectroscopy of monoazo derivatives of chromotropic acid. Russ Chem Bull 1989, 38, 2321. <https://doi.org/10.1007/BF01168079>
- Abraham Raymond J., Haworth Ian S.: 13—Lanthanide‐induced shift (LIS) investigation of the conformation of aryl sulphones using a novel lanthanide–sulphone complexation model. Magnetic Reson in Chemistry 1988, 26, 252. <https://doi.org/10.1002/mrc.1260260314>
- Ruostesuo P., Häkkinen A.‐M., Mattila T.: Multinuclear NMR study of variously substituted sulphonamides and sulphinamides. Magnetic Reson in Chemistry 1987, 25, 189. <https://doi.org/10.1002/mrc.1260250302>
- Brehme Rainer, Stroede Bernd: Aza‐Enamine. VI. Umsetzungen von N,N‐Dialkylhydrazonen aromatischer Aldehyde mit Sulfonylisocyanaten. J. Prakt. Chem. 1987, 329, 246. <https://doi.org/10.1002/prac.19873290214>
- Häkkinen A.‐M, Ruostesuo P.: Carbon‐13, nitrogen‐15, oxygen‐17 and sulphur‐33 NMR chemical shifts of some sulphur amides and related compounds. Magnetic Reson in Chemistry 1985, 23, 424. <https://doi.org/10.1002/mrc.1260230604>