Supporting Information
| Supporting Information File 1: General information, experimental details, characterization data and copies of 1H and 13C NMR spectra, and HPLC experimental data. | ||
| Format: PDF | Size: 4.1 MB | Download |
Cite the Following Article
Construction of highly enantioenriched spirocyclopentaneoxindoles containing four consecutive stereocenters via thiourea-catalyzed asymmetric Michael–Henry cascade reactions
Yonglei Du, Jian Li, Kerong Chen, Chenglin Wu, Yu Zhou and Hong Liu
Beilstein J. Org. Chem. 2017, 13, 1342–1349.
https://doi.org/10.3762/bjoc.13.131
How to Cite
Du, Y.; Li, J.; Chen, K.; Wu, C.; Zhou, Y.; Liu, H. Beilstein J. Org. Chem. 2017, 13, 1342–1349. doi:10.3762/bjoc.13.131
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: 179.7 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Lyapustin, D. N.; Fedotov, V. V.; Ulomsky, E. N.; Rusinov, V. L.; Chupakhin, O. N. Recent advances in the chemistry of two-carbon nitro-containing synthetic equivalents. Успехи химии 2023, 92. doi:10.57634/rcr5077
- Huang, H.; Li, X.; Su, J.; Song, Q. Difluorocarbene-Enabled Synthesis of 3-Substituted-2-oxoindoles from o-Vinylanilines. Chinese Journal of Organic Chemistry 2023, 43, 1146. doi:10.6023/cjoc202210031
- Davis, T. A.; Garza, A. B.; Miller, R. G.; Gardner, S. B.; Fuhrer, T. J.; Campbell, A. B. Thiourea-Catalyzed Amidation of Esters: A New Method for the Preparation of Amides. Letters in Organic Chemistry 2023, 20, 2–10. doi:10.2174/1570178619666220615144433
- Pan, Y.; Ren, W.; Zhang, Z.; Luo, F.; Hou, X.; Li, X.; Yang, Y.-F.; Wang, Y. Tandem 1,6-addition/cyclopropanation/rearrangement reaction of vinylogous para-quinone methides with 3-chlorooxindoles: construction of vicinal quaternary carbon centers. Organic Chemistry Frontiers 2022, 9, 3697–3708. doi:10.1039/d2qo00471b
- Zhou, J.; Chen, B.; Zhang, F.; Xue, J.; He, X.; Peng, C.; Huang, W.; Zhao, Q. Enantioselective Synthesis of Spirocyclopentane Oxindoles Bearing Five Consecutive Stereocenters through Secondary Amine‐Catalyzed [3+2] Cycloaddition. European Journal of Organic Chemistry 2022, 2022. doi:10.1002/ejoc.202200489
- Dočekal, V.; Vopálenská, A.; Měrka, P.; Konečná, K.; Jand’ourek, O.; Pour, M.; Císařová, I.; Veselý, J. Enantioselective Construction of Spirooxindole-Fused Cyclopentanes. The Journal of organic chemistry 2021, 86, 12623–12643. doi:10.1021/acs.joc.1c01116
- Boddy, A. J.; Bull, J. A. Stereoselective synthesis and applications of spirocyclic oxindoles. Organic Chemistry Frontiers 2021, 8, 1026–1084. doi:10.1039/d0qo01085e
- Nosova, E. V.; Lipunova, G. N.; Charushin, V. N.; Chupakhin, O. N. Fluorine-containing indoles: Synthesis and biological activity. Journal of Fluorine Chemistry 2018, 212, 51–106. doi:10.1016/j.jfluchem.2018.05.012
