Supporting Information
|
Supporting Information File 1:
File Name S1.pdf.
Experimental procedures, characterization data, copies of the 1H, 13C NMR spectra, HPLC chromatograms, ORTEP drawing of 3a and the summary of 3a crystallographic information. |
||
| Format: PDF | Size: 8.7 MB | Download |
|
Supporting Information File 2:
File Name S1.cif.
Crystallographic information file of compound 3a. |
||
| Format: CIF | Size: 215.5 KB | Download |
Cite the Following Article
Diastereoselective auxiliary- and catalyst-controlled intramolecular aza-Michael reaction for the elaboration of enantioenriched 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue
Romain Sallio, Stéphane Lebrun, Frédéric Capet, Francine Agbossou-Niedercorn, Christophe Michon and Eric Deniau
Beilstein J. Org. Chem. 2018, 14, 593–602.
https://doi.org/10.3762/bjoc.14.46
How to Cite
Sallio, R.; Lebrun, S.; Capet, F.; Agbossou-Niedercorn, F.; Michon, C.; Deniau, E. Beilstein J. Org. Chem. 2018, 14, 593–602. doi:10.3762/bjoc.14.46
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: 200.3 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Barashkin, A. A.; Polyakov, V. S.; Shikut, N. L.; Putilova, A. D.; Gorovoy, A. R.; Tafeenko, V. A.; Zyk, N. V.; Beloglazkina, E. K. Synthesis of Enantiomerically Pure Thioureas and Thiohydantoins Based on (R)- and (S)-1-(2,4-Dimethoxy-phenyl)ethan-1-amines. Russian Journal of Organic Chemistry 2022, 58, 1362–1367. doi:10.1134/s1070428022090251
- Serusi, L.; Palombi, L.; Pierri, G.; Mola, A. D.; Massa, A. Asymmetric Cascade Aza-Henry/Lactamization Reaction in the Highly Enantioselective Organocatalytic Synthesis of 3-(Nitromethyl)isoindolin-1-ones from α-Amido Sulfones. The Journal of organic chemistry 2022, 87, 8420–8428. doi:10.1021/acs.joc.2c00518
- Samanta, S.; Ali, S. A.; Bera, A.; Giri, S.; Samanta, K. Transition metal-free advanced synthetic approaches for isoindolinones and their fused analogues. New Journal of Chemistry 2022, 46, 7780–7830. doi:10.1039/d2nj00475e
- Sharma, P.; Gupta, R.; Bansal, R. K. Recent advances in organocatalytic asymmetric aza-Michael reactions of amines and amides. Beilstein journal of organic chemistry 2021, 17, 2585–2610. doi:10.3762/bjoc.17.173
- Sánchez-Roselló, M.; Escolano, M.; Gaviña, D.; del Pozo, C. Two Decades of Progress in the Asymmetric Intramolecular aza-Michael Reaction. Chemical record (New York, N.Y.) 2021, 22, e202100161. doi:10.1002/tcr.202100161
- Serusi, L.; Massa, A.; Tedesco, C.; Capobianco, A.; Palombi, L. The First Highly Enantioselective Synthesis of 3-Sulfinyl-Substituted Isoindolinones Having Adjacent Carbon and Sulfur Stereocenters. The Journal of organic chemistry 2021, 86, 10630–10639. doi:10.1021/acs.joc.1c01300
- Escolano, M.; Fernández, J. T.; Rabasa-Alcañiz, F.; Sánchez-Roselló, M.; del Pozo, C. Enantioselective Synthesis of Pyrrolizidinone Scaffolds through Multiple-Relay Catalysis. Organic letters 2020, 22, 9433–9438. doi:10.1021/acs.orglett.0c03344
- Adelantado, F. V. G. Phase-transfer catalysis and the ion pair concept. Physical sciences reviews 2020, 5, 197–228.
- González Adelantado, F. V. Phase-transfer catalysis and the ion pair concept. Physical Sciences Reviews 2020, 0. doi:10.1515/psr-2018-0094
- Gao, W.; Chen, M.-W.; Ding, Q.; Peng, Y. Catalytic Asymmetric Synthesis of Isoindolinones. Chemistry, an Asian journal 2019, 14, 1306–1322. doi:10.1002/asia.201900080
- Ali, S. A.; Bhaumik, S.; Jana, A.; Manna, S. K.; Ikbal, M.; Mandal, A.; Bera, A.; Jana, A.; Samanta, S. NaN3/NH4Cl‐Promoted Aza‐Cyclization: A Convenient Route for Bio‐Active Diverse Isoindolinone Derivatives. ChemistrySelect 2018, 3, 11950–11956. doi:10.1002/slct.201802696
