Supporting Information
Supporting Information File 1: Experimental procedures, characterization data and copies of NMR spectra. | ||
Format: PDF | Size: 7.9 MB | Download |
Cite the Following Article
An intramolecular C–N cross-coupling of β-enaminones: a simple and efficient way to precursors of some alkaloids of Galipea officinalis
Hana Doušová, Radim Horák, Zdeňka Růžičková and Petr Šimůnek
Beilstein J. Org. Chem. 2015, 11, 884–892.
https://doi.org/10.3762/bjoc.11.99
How to Cite
Doušová, H.; Horák, R.; Růžičková, Z.; Šimůnek, P. Beilstein J. Org. Chem. 2015, 11, 884–892. doi:10.3762/bjoc.11.99
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Prieto, A. doi:10.1002/9781119757153.ch8
- Benedetto Tiz, D.; Bagnoli, L.; Rosati, O.; Marini, F.; Sancineto, L.; Santi, C. New Halogen-Containing Drugs Approved by FDA in 2021: An Overview on Their Syntheses and Pharmaceutical Use. Molecules (Basel, Switzerland) 2022, 27, 1643. doi:10.3390/molecules27051643
- Peng, F.; Tan, L.; Chen, L.; Dalby, S. M.; DiRocco, D. A.; Duan, J.; Feng, M.; Gong, G.; Guo, H.; Hethcox, J. C.; Jin, L.; Johnson, H. C.; Kim, J.; Le, D.; Lin, Y.; Liu, W.; Shen, J.; Wan, Y.; Xiao, C.; Xiang, B.; Xiang, Q.; Xu, J.; Yan, L.; Yang, W.; Ye, H.; Yu, Y.; Zhang, J. Manufacturing Process Development for Belzutifan, Part 1: A Concise Synthesis of the Indanone Starting Material. Organic Process Research & Development 2021, 26, 508–515. doi:10.1021/acs.oprd.1c00236
- Muthukrishnan, I.; Sridharan, V.; Menéndez, J. C. Progress in the Chemistry of Tetrahydroquinolines. Chemical reviews 2019, 119, 5057–5191. doi:10.1021/acs.chemrev.8b00567
- Doušová, H.; Růžičková, Z.; Šimůnek, P. Synthesis of N-Substituted Condensed Tetrahydropyridine-Based Enaminones via Palladium-Catalyzed Intramolecular C–N Cross-coupling. Journal of Heterocyclic Chemistry 2018, 55, 670–684. doi:10.1002/jhet.3085
- Diaz-Muñoz, G.; Isidório, R. G.; Miranda, I. L.; de Souza Dias, G. N.; Diaz, M. A. N. A concise and efficient synthesis of tetrahydroquinoline alkaloids using the phase transfer mediated Wittig olefination reaction. Tetrahedron Letters 2017, 58, 3311–3315. doi:10.1016/j.tetlet.2017.07.044
- Young, J.; Schäfer, C.; Solan, A.; Baldrica, A.; Belcher, M.; Nişancı, B.; Wheeler, K. A.; Trivedi, E. R.; Török, B.; Dembinski, R. Regioselective “hydroamination” of alk-3-ynones with non-symmetrical o-phenylenediamines. Synthesis of diversely substituted 3H-1,5-benzodiazepines via (Z)-3-amino-2-alkenones. RSC Advances 2016, 6, 107081–107093. doi:10.1039/c6ra24291j
- Doušová, H.; Horak, R.; Ruzickova, Z.; Simunek, P. An Intramolecular C—N Cross‐Coupling of β‐Enaminones: A Simple and Efficient Way to Precursors of Some Alkaloids of Galipea officinalis. ChemInform 2015, 46. doi:10.1002/chin.201532167