Cite the Following Article
Recent synthesis of thietanes
Jiaxi Xu
Beilstein J. Org. Chem. 2020, 16, 1357–1410.
https://doi.org/10.3762/bjoc.16.116
How to Cite
Xu, J. Beilstein J. Org. Chem. 2020, 16, 1357–1410. doi:10.3762/bjoc.16.116
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: 145.5 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Saejong, P.; Zhong, J.; Rojas, J. J.; White, A. J. P.; Choi, C.; Bull, J. A. Synthesis of 3,3-Disubstituted Thietane Dioxides. The Journal of organic chemistry 2024. doi:10.1021/acs.joc.4c01843
- Patel, D. J.; Chikhalia, K. H. Copper-catalyzed three-component reaction to construct thietane ring using elemental sulfur. Tetrahedron 2024, 166, 134226. doi:10.1016/j.tet.2024.134226
- Di Terlizzi, L.; Nicchio, L.; Protti, S.; Fagnoni, M. Visible photons as ideal reagents for the activation of coloured organic compounds. Chemical Society reviews 2024, 53, 4926–4975. doi:10.1039/d3cs01129a
- Bhanja, R.; Bera, S. K.; Mal, P. Photocatalyst‐ and Transition‐Metal‐Free Light‐Induced Formation of Carbon‐Chalcogen Bonds. Advanced Synthesis & Catalysis 2023, 366, 168–182. doi:10.1002/adsc.202301094
- Zhang, Q.; Yang, Y.; Zhang, S.; Liu, Q. Navigating Visible‐Light‐Triggered (aza and thia) Paternò‐Büchi Reactions for the Synthesis of Heterocycles. Advanced Synthesis & Catalysis 2023, 365, 3556–3571. doi:10.1002/adsc.202300702
- Zhang, M.; Wu, Q.; Xu, J. Lewis Acid‐Mediated Ring Contraction of 2,4‐Diaryl‐2,3‐dihydro‐1H‐1,5‐benzodiazepines: Access to 2‐Aryl‐1‐styrylbenzimidazoles. Helvetica Chimica Acta 2023, 106. doi:10.1002/hlca.202200143
- Franceschi, P.; Cuadros, S.; Goti, G.; Dell'Amico, L. Mechanisms and Synthetic Strategies in Visible Light-Driven [2+2]-Heterocycloadditions. Angewandte Chemie (International ed. in English) 2023, 62, e202217210. doi:10.1002/anie.202217210
- Franceschi, P.; Cuadros, S.; Goti, G.; Dell'Amico, L. Mechanisms and Synthetic Strategies in Visible Light‐Driven [2+2]‐Heterocycloadditions. Angewandte Chemie 2023, 135. doi:10.1002/ange.202217210
- Belen'kii, L. I.; Gazieva, G. A.; Evdokimenkova, Y. B.; Soboleva, N. O. The literature of heterocyclic chemistry, Part XX, 2020. Advances in Heterocyclic Chemistry; Elsevier, 2023; pp 201–274. doi:10.1016/bs.aihch.2022.10.005
- Kaur, B.; Singh, G.; Sharma, V.; Singh, I. Sulphur Containing Heterocyclic Compounds as Anticancer Agents. Anti-cancer agents in medicinal chemistry 2023, 23, 869–881. doi:10.2174/1871520623666221221143918
- Grosse, S.; Tahri, A.; Raboisson, P.; Houpis, Y.; Stoops, B.; Jacoby, E.; Neefs, J.-M.; Van Loock, M.; Goethals, O.; Geluykens, P.; Bonfanti, J.-F.; Jonckers, T. H. M. From Oxetane to Thietane: Extending the Antiviral Spectrum of 2'-Spirocyclic Uridines by Substituting Oxygen with Sulfur. ACS medicinal chemistry letters 2022, 13, 1879–1884. doi:10.1021/acsmedchemlett.2c00372
- Lapuh, M. I.; Cormier, G.; Chergui, S.; Aitken, D. J.; Boddaert, T. Preparation of Thietane Derivatives through Domino Photochemical Norrish Type II/Thia-Paternò-Büchi Reactions. Organic letters 2022, 24, 8375–8380. doi:10.1021/acs.orglett.2c03428
- Song, S.-M.; Jin, J.; Choi, J.-H.; Chung, W.-J. Synthesis of cis-thiiranes as diastereoselective access to epoxide congeners via 4π-electrocyclization of thiocarbonyl ylides. Nature communications 2022, 13, 4818. doi:10.1038/s41467-022-32499-3
- Francisco, K. R.; Ballatore, C. Thietanes and Derivatives thereof in Medicinal Chemistry. Current topics in medicinal chemistry 2022, 22, 1219–1234. doi:10.2174/1568026622666220511154228
- Xu, J. Comprehensive Heterocyclic Chemistry IV - Thietanes and Thietes: Fused and Spiro-Ring Derivatives. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 307–326. doi:10.1016/b978-0-12-818655-8.00151-7
- Malarney, K. P.; Kc, S.; Schmidt, V. A. Recent strategies used in the synthesis of saturated four-membered heterocycles. Organic & biomolecular chemistry 2021, 19, 8425–8441. doi:10.1039/d1ob00988e
- Senatore, R.; Malik, M.; Langer, T.; Holzer, W.; Pace, V. Consecutive and Selective Double Methylene Insertion of Lithium Carbenoids to Isothiocyanates: A Direct Assembly of Four‐Membered Sulfur‐Containing Cycles. Angewandte Chemie 2021, 133, 25058–25062. doi:10.1002/ange.202110641
- Senatore, R.; Malik, M.; Langer, T.; Holzer, W.; Pace, V. Consecutive and Selective Double Methylene Insertion of Lithium Carbenoids to Isothiocyanates: A Direct Assembly of Four-Membered Sulfur-Containing Cycles. Angewandte Chemie (International ed. in English) 2021, 60, 24854–24858. doi:10.1002/anie.202110641
- Kataev, V. A.; Mesheryakova, S. A.; Mesheryakova, E. S.; Tyumkina, T. V.; Khalilov, L. M.; Lazarev, V. V.; Kuznetsov, V. V. Synthesis, Structure, and Conformational Analysis of N-(2,4-Dichlorophenyl)-2-[6-methyl-2,4-dioxo-3-(thietan-3-yl)-1,2,3,4-tetrahydropyrimidine-1-yl]acetamide. Russian Journal of General Chemistry 2021, 91, 785–791. doi:10.1134/s1070363221050054
- Anaya, J.; Sánchez, R. M. Four-membered ring systems. Progress in Heterocyclic Chemistry; Elsevier, 2021; pp 53–91. doi:10.1016/b978-0-323-98410-2.00004-7