Supporting Information
| Supporting Information File 1: Experimental procedures and NMR spectra. | ||
| Format: PDF | Size: 5.3 MB | Download |
Cite the Following Article
Study on the synthesis of the cyclopenta[f]indole core of raputindole A
Nils Marsch, Mario Kock and Thomas Lindel
Beilstein J. Org. Chem. 2016, 12, 334–342.
https://doi.org/10.3762/bjoc.12.36
How to Cite
Marsch, N.; Kock, M.; Lindel, T. Beilstein J. Org. Chem. 2016, 12, 334–342. doi:10.3762/bjoc.12.36
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: 101.1 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- He, Y.; Wang, Q.; Yin, H.; Chen, F.-X. Copper(I)-catalyzed electrophilic thiocyanation/dearomatization/spirocyclization of benzofurans to synthesize benzannulated spiroketals. Organic & biomolecular chemistry 2023, 21, 4216–4219. doi:10.1039/d3ob00438d
- Kumar, B. R.; Kumar, A. K.; Reddy, B. S.; Shashikala, K.; Laxminarayana, E. Synergic Synthesis and Characterization of tert-Butyl 4-[(E)-But-1-en-3-yn-1-yl]-3-{[tert-butyl(dimethyl)silyl]oxy}-1H-indole-1-carboxylate. Russian Journal of Organic Chemistry 2022, 58, 580–583. doi:10.1134/s1070428022040169
- Justaud, F.; Hachem, A.; Grée, R. Recent Developments in the Meyer‐Schuster Rearrangement. European Journal of Organic Chemistry 2021, 2021, 514–542. doi:10.1002/ejoc.202001494
- Fresia, M.; Kock, M.; Lindel, T. Synthesis of (-)-Dihydroraputindole D by Enantioselective Benzoylation of a 1,3-Diol Intermediate. Chemistry (Weinheim an der Bergstrasse, Germany) 2020, 26, 12733–12737. doi:10.1002/chem.202002579
- Regueira, J. L. L. F.; Silva, L. F.; Pilli, R. A. Total Synthesis of (+)-Raputindole A: An Iridium-Catalyzed Cyclization Approach. Organic letters 2020, 22, 6262–6266. doi:10.1021/acs.orglett.0c01943
- Kock, M.; Lindel, T. Diastereoselective Total Synthesis of Raputindole A. Organic letters 2018, 20, 5444–5447. doi:10.1021/acs.orglett.8b02349
- Congmon, J.; Tius, M. A. Contiguous Quaternary Centers from a AuI-Catalyzed Nazarov Cyclization. European Journal of Organic Chemistry 2018, 2018, 2926–2930. doi:10.1002/ejoc.201800604
- Kock, M.; Jones, P. G.; Lindel, T. Total Synthesis and Absolute Configuration of Raputindole A. Organic letters 2017, 19, 6296–6299. doi:10.1021/acs.orglett.7b03014
- Marsch, N.; Kock, M.; Lindel, T. Study on the Synthesis of the Cyclopenta[f]indole Core of Raputindole A. ChemInform 2016, 47. doi:10.1002/chin.201622032
