Supporting Information
Supporting Information File 1: All experimental details, 1H and 13C NMR spectra for compounds 6a–f and 8a–f and X-ray crystallographic data for 8c. | ||
Format: PDF | Size: 1.1 MB | Download |
Cite the Following Article
Use of mixed Li/K metal TMP amide (LiNK chemistry) for the synthesis of [2.2]metacyclophanes
Marco Blangetti, Patricia Fleming and Donal F. O'Shea
Beilstein J. Org. Chem. 2011, 7, 1249–1254.
https://doi.org/10.3762/bjoc.7.145
How to Cite
Blangetti, M.; Fleming, P.; O'Shea, D. F. Beilstein J. Org. Chem. 2011, 7, 1249–1254. doi:10.3762/bjoc.7.145
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.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Martyanov, T. P.; Vorozhtsov, A. P.; Ushakov, E. N.; Slesarenko, N. A.; Sulimenkov, I. V.; Gromov, S. P. Self-assembly via hydrogen bonding of bis(18-crown-6)-1,3-distyrylbenzene and [2 + 2] photocycloaddition: Stereoselective synthesis of [2.2]metacyclophanes and butterfly-type thermal isomerization. Tetrahedron Chem 2024, 12, 100091. doi:10.1016/j.tchem.2024.100091
- Li, Y.; Wu, W.; Zhu, H.; Kang, Q.; Xu, L.; Shi, H. Rhodium‐Catalyzed Benzylic Addition Reactions of Alkylarenes to Michael Acceptors. Angewandte Chemie 2022, 134. doi:10.1002/ange.202207917
- Li, Y.; Wu, W.-Q.; Zhu, H.; Kang, Q.-K.; Xu, L.; Shi, H. Rhodium-Catalyzed Benzylic Addition Reactions of Alkylarenes to Michael Acceptors. Angewandte Chemie (International ed. in English) 2022, 61, e202207917. doi:10.1002/anie.202207917
- Blangetti, M.; O'Shea, D. F. Chiral auxiliary-mediated synthesis of planar chiral [2.2]metacyclophanes. Tetrahedron Letters 2020, 61, 152492. doi:10.1016/j.tetlet.2020.152492
- Arnodo, D.; Ghinato, S.; Nejrotti, S.; Blangetti, M.; Prandi, C. Lateral lithiation in deep eutectic solvents: regioselective functionalization of substituted toluene derivatives. Chemical communications (Cambridge, England) 2020, 56, 2391–2394. doi:10.1039/d0cc00593b
- Saikia, I.; Borah, A. J.; Phukan, P. Use of Bromine and Bromo-Organic Compounds in Organic Synthesis. Chemical reviews 2016, 116, 6837–7042. doi:10.1021/acs.chemrev.5b00400
- Manvar, A.; Fleming, P.; O'Shea, D. F. General Ambient Temperature Benzylic Metalations Using Mixed-Metal Li/K-TMP Amide. The Journal of organic chemistry 2015, 80, 8727–8738. doi:10.1021/acs.joc.5b01540
- Mulvey, R. E.; Robertson, S. D. Synthetically Important Alkali‐Metal Utility Amides: Lithium, Sodium, and Potassium Hexamethyldisilazides, Diisopropylamides, and Tetramethylpiperidides. Angewandte Chemie (International ed. in English) 2013, 52, 11470–11487. doi:10.1002/anie.201301837
- Mulvey, R. E.; Robertson, S. D. Nützliche Alkalimetallamide für die Synthese: Lithium‐, Natrium‐ und Kaliumhexamethyldisilazide, ‐diisopropylamide und ‐tetramethylpiperidide. Angewandte Chemie 2013, 125, 11682–11700. doi:10.1002/ange.201301837
- Das, M.; O'Shea, D. F. Synthesis and application of benzyl-TMS derivatives as bench stable benzyl anion equivalents. Tetrahedron 2013, 69, 6448–6460. doi:10.1016/j.tet.2013.05.078
- Blangetti, M.; Müller-Bunz, H.; O'Shea, D. F. First asymmetric synthesis of planar chiral [2.2]metacyclophanes. Chemical communications (Cambridge, England) 2013, 49, 6125–6127. doi:10.1039/c3cc42275e
- Blangetti, M.; Müller-Bunz, H.; O'Shea, D. F. Synthesis, separation, and structural analysis of planar chiral carboxy-substituted [2.2]metacyclophanes. Tetrahedron 2013, 69, 4285–4291. doi:10.1016/j.tet.2013.03.076
- Mulvey, R. E.; Robertson, S. D. FascinATES: Mixed-Metal Ate Compounds That Function Synergistically. Topics in Organometallic Chemistry; Springer International Publishing, 2013; pp 129–158. doi:10.1007/3418_2013_73
- Blangetti, M.; Fleming, P.; O'Shea, D. F. Homo- and Hetero-oxidative Coupling of Benzyl Anions. The Journal of organic chemistry 2012, 77, 2870–2877. doi:10.1021/jo3000805