Supporting Information
| Supporting Information File 1: Synthetic procedures, characterization data and copies of spectra. | ||
| Format: PDF | Size: 13.0 MB | Download |
Cite the Following Article
Synthesis of (Z)-3-[amino(phenyl)methylidene]-1,3-dihydro-2H-indol-2-ones using an Eschenmoser coupling reaction
Lukáš Marek, Lukáš Kolman, Jiří Váňa, Jan Svoboda and Jiří Hanusek
Beilstein J. Org. Chem. 2021, 17, 527–539.
https://doi.org/10.3762/bjoc.17.47
How to Cite
Marek, L.; Kolman, L.; Váňa, J.; Svoboda, J.; Hanusek, J. Beilstein J. Org. Chem. 2021, 17, 527–539. doi:10.3762/bjoc.17.47
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.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 9.0 MB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Shirazi, H.; Imani, K.; Notash, B.; Bazgir, A. Diastereoselective Synthesis of 3-(Aminoalkylidene)oxindoles via a Nucleophilic Vinylic Substitution of 2-Chloropyridinium Salts. The Journal of organic chemistry 2025, 90, 14363–14372. doi:10.1021/acs.joc.5c00728
- Purahong, N.; Teerawatananond, T.; Chotsaeng, N.; Janthakit, P.; Nalaoh, P.; Promarak, V.; Kuhakarn, C.; Meesin, J. DBU‐Mediated Reaction of 3‐Chlorooxindole and 9‐Xanthyl Fluorene for Synthesis of 3‐Arylidene Oxindole. Asian Journal of Organic Chemistry 2025, 14. doi:10.1002/ajoc.202400660
- Song, D.; Chen, R.; Huang, W.; Yang, P.; Chen, L.; Zhang, J.; Ling, F.; Zhong, W. Room‐Temperature Synthesis of α‐Alkylated Indolin‐2‐ones via a Photo Assisted Iron Catalyzed Borrowing Hydrogen Reaction. Advanced Synthesis & Catalysis 2024, 366, 1893–1898. doi:10.1002/adsc.202301219
- Duez, Q.; Marek, L.; Váňa, J.; Hanusek, J.; Roithová, J. Autocatalysis in Eschenmoser Coupling Reactions. Chemistry (Weinheim an der Bergstrasse, Germany) 2023, 30, e202303619. doi:10.1002/chem.202303619
- Topanov, P. A.; Dmitriev, M. V.; Balandina, S. Y.; Shklyaev, Y. V.; Mashevskaya, I. V.; Maslivets, A. N. Pseudo-three-component spiro[dihydrofuran-2,3′-oxindoles] synthesis: in situ generation of diazooxindole. Журнал общей химии 2023, 93, 1680–1689. doi:10.31857/s0044460x23110057
- Topanov, P. A.; Dmitriev, M. V.; Balandina, S. Y.; Mashevskaya, I. V.; Shklyaev, Y. V.; Maslivets, A. N. Pseudo-Three-Component Spiro[dihydrofuran-2,3′-oxindoles] Synthesis: In Situ Generation of Diazooxindole. Russian Journal of General Chemistry 2023, 93, S482–S490. doi:10.1134/s1070363223150100
- Hanusek, J.; Marek, L.; Váňa, J.; Svoboda, J.; Svobodová, M. Efficient Synthesis of (Z)-4-((Substituted phenylamino)methylidene)isoquinoline-1,3(2H,4H)-diones Using the Eschenmoser Coupling Reaction. Synthesis 2023, 56, 518–526. doi:10.1055/a-2198-1589
- Soam, P.; Mandal, D.; Tyagi, V. Divergent and Selective Synthesis of 3-Alkylidene Oxindoles Using Pd-Catalyzed Multicomponent Reaction. The Journal of organic chemistry 2023, 88, 11023–11035. doi:10.1021/acs.joc.3c00994
- Marek, L.; Váňa, J.; Svoboda, J.; Hanusek, J. Eschenmoser coupling reactions starting from primary thioamides. When do they work and when not?. Beilstein journal of organic chemistry 2023, 19, 808–819. doi:10.3762/bjoc.19.61
- Han, Y.-F.; Lv, G.-F.; Li, Y.; Wu, L.-J.; Ouyang, X.-H.; Li, J.-H. The transient-chelating-group-controlled stereoselective Rh(i)-catalyzed silylative aminocarbonylation of 2-alkynylanilines: access to (Z)-3-(silylmethylene)indolin-2-ones. Chemical science 2022, 13, 9425–9431. doi:10.1039/d2sc03009h
- Secka, J.; Pal, A.; Acquah, F. A.; Mooers, B. H. M.; Karki, A. B.; Mahjoub, D.; Fakhr, M. K.; Wallace, D. R.; Okada, T.; Toyooka, N.; Kuta, A.; Koduri, N.; Herndon, D.; Roberts, K. P.; Wang, Z.; Hileman, B.; Rajagopal, N.; Hussaini, S. R. Coupling of acceptor-substituted diazo compounds and tertiary thioamides: synthesis of enamino carbonyl compounds and their pharmacological evaluation. RSC advances 2022, 12, 19431–19444. doi:10.1039/d2ra02415b
- Marek, L.; Váňa, J.; Svoboda, J.; Hanusek, J. Synthesis of the Kinase Inhibitors Nintedanib, Hesperadin, and Their Analogues Using the Eschenmoser Coupling Reaction. The Journal of organic chemistry 2021, 86, 10621–10629. doi:10.1021/acs.joc.1c01269
Patents
- YIN NING; JI NAN. COMPOUNDS FOR TREATING POLYQ-RELATED NEURODEGENERATIVE DISORDERS. WO 2023104170 A1, June 15, 2023.