Supporting Information
Experimental section, copies of 1H and 13C NMR spectra of compounds, Cartesian coordinates and CIF files of 5a and 7h.
| Supporting Information File 1: Experimental section, copies of 1H and 13C NMR spectra of compounds and Cartesian coordinates. | ||
| Format: PDF | Size: 3.1 MB | Download |
| Supporting Information File 2: CIF file of compound 5a. | ||
| Format: CIF | Size: 16.5 KB | Download |
| Supporting Information File 3: CIF file of compound 7h. | ||
| Format: CIF | Size: 12.4 KB | Download |
Cite the Following Article
Scope and mechanism of the highly stereoselective metal-mediated domino aldol reactions of enolates with aldehydes
M. Emin Cinar, Bernward Engelen, Martin Panthöfer, Hans-Jörg Deiseroth, Jens Schlirf and Michael Schmittel
Beilstein J. Org. Chem. 2016, 12, 813–824.
https://doi.org/10.3762/bjoc.12.80
How to Cite
Cinar, M. E.; Engelen, B.; Panthöfer, M.; Deiseroth, H.-J.; Schlirf, J.; Schmittel, M. Beilstein J. Org. Chem. 2016, 12, 813–824. doi:10.3762/bjoc.12.80
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- Bastos, E. L.; Machado, C. O. Patai's Chemistry of Functional Groups - Recent Advances in Acid–Base and Solvation Properties of Metal Phenolates. Patai's Chemistry of Functional Groups 2017, 1–60. doi:10.1002/9780470682531.pat0848
- Cinar, M. E.; Schmittel, M. Highly stereoselective metal-mediated domino aldol reactions of propiophenone enolates with heteroaromatic, aliphatic, and unsaturated aldehydes. Monatshefte für Chemie - Chemical Monthly 2016, 147, 1925–1932. doi:10.1007/s00706-016-1841-4
- Cinar, M. E.; Engelen, B.; Panthoefer, M.; Deiseroth, H. J.; Schlirf, J.; Schmittel, M. Scope and Mechanism of the Highly Stereoselective Metal-Mediated Domino Aldol Reactions of Enolates with Aldehydes. ChemInform 2016, 47. doi:10.1002/chin.201630163
- Kulkarni, A. A. Highlights from the Flow Chemistry Literature 2016 (Part 1). Journal of Flow Chemistry 2016, 6, 126–133. doi:10.1556/1846.2016.11111
