Supporting Information
| Supporting Information File 1: Experimental procedures, NMR (1H, 13C, 19F) and IR spectra of synthesized compounds. | ||
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| Supporting Information File 2: Crystal and structure refinement data for compounds 11, 12c, 12d and 19. | ||
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Cite the Following Article
Reactions of 3-aryl-1-(trifluoromethyl)prop-2-yn-1-iminium salts with 1,3-dienes and styrenes
Thomas Schneider, Michael Keim, Bianca Seitz and Gerhard Maas
Beilstein J. Org. Chem. 2020, 16, 2064–2072.
https://doi.org/10.3762/bjoc.16.173
How to Cite
Schneider, T.; Keim, M.; Seitz, B.; Maas, G. Beilstein J. Org. Chem. 2020, 16, 2064–2072. doi:10.3762/bjoc.16.173
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Scholarly Works
- Gerster, H.; Keim, M.; Maas, G. Iminium-substituted 2,3-dihydroisoxazoles: synthesis from acetylenic iminium salts and nitrones, and some transformations. Zeitschrift für Naturforschung B 2022, 77, 505–515. doi:10.1515/znb-2022-0014
- Seitz, B.; Maas, G. Reactions of 1-trifluoromethyl-prop-2-yne1-iminium salts with 2- and 3-aminopyridines. Zeitschrift für Naturforschung B 2022, 77, 517–529. doi:10.1515/znb-2022-0018
- Pan, L.; Wang, Q.; Sun, J.; Yan, C.-G. Intramolecular Diels−Alder reaction of styrene with phenoxy-acrylate for construction of functionalized naphthalenes. Asian Journal of Organic Chemistry 2021, 10, 2591–2595. doi:10.1002/ajoc.202100401
- Schneider, T.; Fleischmann, M.; Hergesell, D.; Majstorović, N.; Maas, G. A Convenient Synthesis of 4-CF3-Quinolines from 1-Trifluoromethyl-prop-2-yne 1-Iminium Salts and Arylamines. European Journal of Organic Chemistry 2021, 2021, 2869–2886. doi:10.1002/ejoc.202100378
- Schneider, T.; Heinrich, G.; Koch, R.; Maas, G. Reactions of a 3-Phenyl-1-trifluoromethyl-prop-2-yne Iminium Salt with Furans, Thiophenes, and Pyrroles. European Journal of Organic Chemistry 2021, 2021, 1011–1025. doi:10.1002/ejoc.202001577
- Maas, G.; Koch, R. 1-Trifluoromethyl-prop-2-yne 1-iminium salts and 1-imines: reactions with the mesoionic "Nitron". Zeitschrift für Naturforschung B 2020, 75, 1065–1074. doi:10.1515/znb-2020-0178
