Stereoselective Synthesis of Chiral C2-Symmetric 1,3- and 1,5-Bissulfoxides Guided by Horeau Principle: Understanding the Influence of the Carbon Chain Nature in its Ability for Metal Coordination [Dataset]

2024-12-172024-12-172024-07-172024-12-17Moreno Rodríguez, N., Prieto Ramírez, L.A.,...,Fernández Fernández, I. (2024). Stereoselective Synthesis of Chiral C2-Symmetric 1,3- and 1,5-Bissulfoxides Guided by Horeau Principle: Understanding the Influence of the Carbon Chain Nature in its Ability for Metal Coordination [Dataset]. idUS (Depósito de Investigación de la Universidad de Sevilla). https://doi.org/10.12795/11441/165883.https://hdl.handle.net/11441/165883Diastereomeric excess determination of 1,3-bisulfinates. Experimental data of 1,3-bis-(sulfinyl)propanes. Experimental data of allylation of N-(benzoyl)isobutylhydrazone. Experimental data of vinyl sulfoxides. Experimental data of 1,5-bis(sulfinyl)-3-thioderivatives. Figures of regioselective oxidation of 1,5-bis(sulfinyl)-3-thioderivatives. Figures of palladium(II) and ruthenium(II) complexes formation. HPLC chromatograms of selected compounds. 1H NMR, 13C{1H} NMR and 19F NMR of selected compounds. 2D NMR of selected compounds. X-ray Structural Analysis for (CDCC 2309479).application/pdfengAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/Síntesis estereoselectivaLey de HoreauLigandos quirales C2 simétricosBis-sulfóxidosStereoselective SynthesisHoreau PrincipleChiral C2‑Symmetric ligandsBis- SulfoxidesStereoselective Synthesis of Chiral C2-Symmetric 1,3- and 1,5-Bissulfoxides Guided by Horeau Principle: Understanding the Influence of the Carbon Chain Nature in its Ability for Metal Coordination [Dataset]info:eu-repo/semantics/datasetinfo:eu-repo/semantics/openAccess10.12795/11441/165883