1,2-ジオキソラン
1,2-ジオキソラン
出典: フリー百科事典『ウィキペディア（Wikipedia）』 (2021/05/29 15:21 UTC 版)
1,2-ジオキソラン (1,2-Dioxolane) は、C3H6O2 の化学式で表され、3つの炭素と 2つの隣接した酸素を持つ環状化合物である。構造式は [-(CH2)3-O-O-] と書くこともできる[1][2] 。この化合物は有機過酸化物（具体的にはエンドペルオキシド）で、しばしば単に「ジオキソラン」と呼ばれるより一般的な 1,3-ジオキソラン の構造異性体である。
- ^ Tsan H. Lay and Joseph W. Bozzelli (1997): "Enthalpies of formation of cyclic alkyl peroxides: dioxirane, 1,2-dioxetane, 1,2-dioxolane, and 1,2-dioxane". Chemical Physics Letters, volume 268, issues 1–2, pages 175-179. doi:10.1016/S0009-2614(97)00168-1
- ^ "C3H6O2 1,2-dioxolane". Landolt-Börnstein - Group II Molecules and Radicals 14A - Elements with two or three internal rotors (Diamagnetic Molecules). doi:10.1007/10201404_40
- ^ Takeshi Akasaka, Koichiro Fukuoka, and Wataru Ando (1991): "Formation of 1,2-dioxolane in the singlet oxygenation of cyclopropane". Tetrahedron Letters, volume 32, issue 52, pages 7695-7698. doi:10.1016/0040-4039(91)80568-QG
- ^ Ken S. Feldman and Robert E. Simpson (1989): "Stereochemical studies on the preparation and subsequent reductive cleavage of 1,2-dioxolanes. Application to the synthesis of (±)-yashabushitriol". Tetrahedron Letters, volume 30, issue 50, pages 6985-6988. doi:10.1016/S0040-4039(01)93404-5
- ^ Sergio Mata, Jesús González, Rubén Vicente, Luis A. López (2016): "Zinc‐catalyzed multicomponent reactions: Easy access to furyl‐Substituted cyclopropane and 1,2‐dioxolane derivatives". European Journal of Organic Chemistry, volume 2016, issue 15, pages 2681-2687. doi:10.1002/ejoc.201600393
- ^ a b c Jean-Jacques Helesbeux, Damien Peyronnet, Mehdi Labaïed, Philippe Grellier, François Frappier, Denis Seraphin, Pascal Richomme, and Olivier Duval (2002): "Synthesis and antimalarial activity of some new 1,2-doxolane derivatives". Journal of Enzyme Inhibition and Medicinal Chemistry, volume 17, issue 6, pages 431-437. doi:10.1080/1475636021000005677
- ^ a b Derek C. Martyn, Armando P. Ramirez, Meaghan J. Beattie, Joseph F. Cortese, Vishal Patel, Margaret A.Rush, K. A. Woerpel, and Jon Clardy (2008): "Synthesis of spiro-1,2-dioxolanes and their activity against Plasmodium falciparum". Bioorganic & Medicinal Chemistry Letters, volume 18, issue 24, pages 6521-6524. doi:10.1016/j.bmcl.2008.10.083
- ^ He-Hua Liu, Hong-Xia Jin, and Yi-Kang Wu (2004): "Synthesis and cleavage studies of a 1,2-dioxolane-type peroxide". Chinese Journal of Chemistry, volume 22, issue 9, pages 1029-1033. doi:10.1002/cjoc.20040220930
- ^ A. J. Bloodworth and Neil A. Tallant (1992): "1,2,4-Trioxane versus 1,2-dioxolane formation in the mercury(II) acetate-mediated cyclisation of hemiperoxyacetals derived from allylic hydroperoxides". Journal of the Chemical Society, Chemical Communications,volume 1992, issue 5, doi:10.1039/C39920000428
- ^ A. J. Bloodworth, Brian D. Bothwell, Andrew N. Collins, and Nicola L. Maidwell (1996): "A short synthesis of naturally occurring and other analogues of plakinic acids that contain the 1,2-dioxolane group". Tetrahedron Letters, volume 37, issue 11, pages 1885-1888. doi:10.1016/0040-4039(96)00143-8
- ^ a b Douglas W. Phillipson and Kenneth L. Rinehart Jr. (1983): "Antifungal peroxide-containing acids from two Caribbean sponges". Journal of the American Chemical Association, volume 105, issue 26, pages 7735–7736. doi:10.1021/ja00364a045
- ^ Peng Dai, Tony K. Trullinger, Xuejun Liu, and Patrick H. Dussault (2006): "Asymmetric synthesis of 1,2-dioxolane-3-acetic acids: Synthesis and configurational cssignment of plakinic acid A". Journal of Organic Chemistry, volume 71, issue 6, pages 2283–2292. doi:10.1021/jo0522254
- ^ Wynne V. Kandur, Kathleen J. Richert, Curtis J. Rieder, Andrew M. Thomas, Chunhua Hu, Joseph W. Ziller, and K. A. Woerpel (2014): "Synthesis and reactivity of 1,2-dioxolanes from β,γ-epoxy ketones". rganic letters, volume 16, issue 10, pages 2650–2653. doi:10.1021/ol500835f
- ^ "C3F6O2 Hexafluoro-1,2-dioxolane". Landolt-Börnstein - Group II Molecules and Radicals 25C (Molecules containing Three or Four Carbon Atoms). doi:10.1007/10688787_30
[続きの解説]
「1,2-ジオキソラン」の続きの解説一覧
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