Rujukan Tetrahidrofuran

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  2. 1 2 3 4 5 6 NIOSH Pocket Guide to Chemical Hazards. "#0602" (dalam bahasa Inggeris). National Institute for Occupational Safety and Health (NIOSH).
  3. 1 2 3 Baird, Zachariah Steven; Uusi-Kyyny, Petri; Pokki, Juha-Pekka; Pedegert, Emilie; Alopaeus, Ville (6 Nov 2019). "Vapor Pressures, Densities, and PC-SAFT Parameters for 11 Bio-compounds". International Journal of Thermophysics. 40 (11): 102. Bibcode:2019IJT....40..102B. doi:10.1007/s10765-019-2570-9.
  4. ↑ NIST Chemistry WebBook. http://webbook.nist.gov
  5. 1 2 3 Templat:GESTIS
  6. 1 2 "Tetrahydrofuran". Immediately Dangerous to Life or Health Concentrations (IDLH). Institut Kebangsaan untuk Keselamatan dan Kesihatan Pekerjaan (NIOSH).
  7. "New Environment Inc. - NFPA Chemicals". Newenv.com. Dicapai pada 2016-07-16.
  8. ↑ Müller, Herbert (2005), "Tetrahydrofuran", Ullmann's Encyclopedia of Industrial Chemistry (dalam bahasa Inggeris), Weinheim: Wiley-VCH, doi:10.1002/14356007.a26_221
  9. ↑ "Ethers". Kirk‑Othmer Encyclopedia of Chemical Technology. John Wiley & Sons. 2004.
  10. ↑ Morrison, Robert Thornton; Boyd, Robert Neilson (1972). Organic Chemistry (ed. 2nd). Allyn and Bacon. m/s. 569.
  11. ↑ Hoydonckx, H. E.; Rhijn, W. M. Van; Rhijn, W. Van; Vos, D. E. De; Jacobs, P. A. (2007), "Furfural and Derivatives", Ullmann's Encyclopedia of Industrial Chemistry (dalam bahasa Inggeris), American Cancer Society, doi:10.1002/14356007.a12_119.pub2, ISBN 978-3-527-30673-2
  12. ↑ "Polyethers, Tetrahydrofuran and Oxetane Polymers". Kirk‑Othmer Encyclopedia of Chemical Technology. John Wiley & Sons. 1996.
  13. ↑ "Chemical Reactivity". Michigan State University. Diarkibkan daripada yang asal pada 2010-03-16. Dicapai pada 2010-02-15.
  14. ↑ "NMR–MRI study of clathrate hydrate mechanisms" (PDF). Fileave.com. Diarkibkan daripada yang asal (PDF) pada 2011-07-11. Dicapai pada 2010-02-15.
  15. ↑ Cai, Charles; Zhang, Taiying; Kumar, Rajeev; Wyman, Charles (13 August 2013). "THF co-solvent enhances hydrocarbon fuel precursor yields from lignocellulosic biomass". Green Chemistry. 15 (11): 3140–3145. doi:10.1039/C3GC41214H.
  16. ↑ Lucht, B. L.; Collum, D. B. (1999). "Lithium Hexamethyldisilazide: A View of Lithium Ion Solvation through a Glass-Bottom Boat". Accounts of Chemical Research. 32 (12): 1035–1042. doi:10.1021/ar960300e.
  17. ↑ Elschenbroich, C.; Salzer, A. (1992). Organometallics: A Concise Introduction (ed. 2nd). Weinheim: Wiley-VCH. ISBN 3-527-28165-7.
  18. ↑ Williams, D. B. G.; Lawton, M. (2010). "Drying of Organic Solvents: Quantitative Evaluation of the Efficiency of Several Desiccants". Journal of Organic Chemistry. 75 (24): 8351–4. doi:10.1021/jo101589h. PMID 20945830.
  19. ↑ F.A.Cotton, S.A.Duraj, G.L.Powell, W.J.Roth (1986). "Comparative Structural Studies of the First Row Early Transition Metal(III) Chloride Tetrahydrofuran Solvates". Inorg. Chim. Acta. 113: 81. doi:10.1016/S0020-1693(00)86863-2.CS1 maint: multiple names: authors list (link)
  20. ↑ Vogel G. C.; Drago, R. S. (1996). "The ECW Model". Journal of Chemical Education. 73 (8): 701–707. Bibcode:1996JChEd..73..701V. doi:10.1021/ed073p701.
  21. ↑ Manzer, L. E. "Tetrahydrofuran Complexes of Selected Early Transition Metals," Inorganic Synthesis. 21, 135–140, (1982).
  22. ↑ "Material Safety Data Sheet Tetrahydrofuran, 99.5+%, for spectroscopy". Fisher Scientific. Dicapai pada 2022-07-27.
  23. ↑ Lorente, Adriana; Lamariano-Merketegi, Janire; Albericio, Fernando; Álvarez, Mercedes (2013). "Tetrahydrofuran-Containing Macrolides: A Fascinating Gift from the Deep Sea". Chemical Reviews. 113 (7): 4567–4610. doi:10.1021/cr3004778. PMID 23506053.
  24. ↑ Wolfe, John P.; Hay, Michael B. (2007). "Recent advances in the stereoselective synthesis of tetrahydrofurans". Tetrahedron. 63 (2): 261–290. doi:10.1016/j.tet.2006.08.105. PMC 1826827. PMID 18180807.
  25. ↑ Cremer, Dieter (1983). "Theoretical Determination of Molecular Structure and Conformation. XI. The Puckering of Oxolanes". Israel Journal of Chemistry. 23: 72–84. doi:10.1002/ijch.198300010.