Supporting Information
| Supporting Information File 1: Experimental details for the preparation of the compounds 3a–g, 5e, 7a,c, 8e, their spectroscopic and analytical data, and 1H and 13C NMR spectra. | ||
| Format: PDF | Size: 2.0 MB | Download |
| Supporting Information File 2: Details of computational studies: Cartesian coordinates, computed geometries of compounds, transition states, and computed total energies. | ||
| Format: PDF | Size: 302.5 KB | Download |
Cite the Following Article
Less reactive dipoles of diazodicarbonyl compounds in reaction with cycloaliphatic thioketones – First evidence for the 1,3-oxathiole–thiocarbonyl ylide interconversion
Valerij A. Nikolaev, Alexey V. Ivanov, Ludmila L. Rodina and Grzegorz Mlostoń
Beilstein J. Org. Chem. 2013, 9, 2751–2761.
https://doi.org/10.3762/bjoc.9.309
How to Cite
Nikolaev, V. A.; Ivanov, A. V.; Rodina, L. L.; Mlostoń, G. Beilstein J. Org. Chem. 2013, 9, 2751–2761. doi:10.3762/bjoc.9.309
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- Medvedev, J. J.; Meleshina, M. V.; Panikorovskii, T. L.; Schneider, C.; Nikolaev, V. A. Domino reactions of diazodicarbonyl compounds with α,β-unsaturated δ-amino esters: a convenient way towards 2-oxopiperidines, dihydropyridinones and isoquinolinediones. Organic & biomolecular chemistry 2015, 13, 9107–9117. doi:10.1039/c5ob01197c
- Mereshchenko, A. S.; Ivanov, A. V.; Baranovskii, V. I.; Mlostoń, G.; Rodina, L. L.; Nikolaev, V. A. On the strong difference in reactivity of acyclic and cyclic diazodiketones with thioketones: experimental results and quantum-chemical interpretation. Beilstein journal of organic chemistry 2015, 11, 504–513. doi:10.3762/bjoc.11.57
- Mlostoń, G.; Pipiak, P.; Linden, A.; Heimgartner, H. 1,3‐Dipolar Cycloadditions of α‐Diazo Ketones Derived from N‐Protected (S)‐Proline with Aromatic and Cycloaliphatic Thioketones. Helvetica Chimica Acta 2015, 98, 190–200. doi:10.1002/hlca.201400334
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