Chemiluminescence during interaction of 1,2,4-trioxolanes and 1,2,4,5-tetraoxanes with iron compounds

被引:0
|
作者
D. V. Kazakov
M. Yu. Ovchinnikov
F. E. Safarov
A. R. Timerbaev
机构
[1] Ufa Scientific Center,Institute of Organic Chemistry
[2] Russian Academy of Sciences,undefined
来源
Russian Chemical Bulletin | 2011年 / 60卷
关键词
trioxolanes; tetraoxanes; chemiluminescence; triterpenoids;
D O I
暂无
中图分类号
学科分类号
摘要
The reaction of triterpene 1,2,4-trioxolanes with the system FeCl3-L-cysteine hydrochloride in the presence of rhodamine G is accompanied by chemiluminescence, whose emitter is an excited dye molecule. Light emission was also found in the biologically important reaction of 1,2,4,5-tetraoxanes with Fe2+ ions in aqueous acetonitrile.
引用
收藏
页码:373 / 375
页数:2
相关论文
共 50 条
  • [41] Comparative Antimalarial Activities and ADME Profiles of Ozonides (1,2,4-trioxolanes) OZ277, OZ439, and Their 1,2-Dioxolane, 1,2,4-Trioxane, and 1,2,4,5-Tetraoxane Isosteres
    Wang, Xiaofang
    Dong, Yinxiang
    Wittlin, Sergio
    Charman, Susan A.
    Chiu, Francis C. K.
    Chollet, Jacques
    Katneni, Kasiram
    Mannila, Janne
    Morizzi, Julia
    Ryan, Eileen
    Scheurer, Christian
    Steuten, Jessica
    Tomas, Josefina Santo
    Snyder, Christopher
    Vennerstrom, Jonathan L.
    JOURNAL OF MEDICINAL CHEMISTRY, 2013, 56 (06) : 2547 - 2555
  • [42] Electroreduction of 1,2,4-trioxolanes generated from ozonation of sunflower oil methyl esters
    Soriano, Nestor U., Jr.
    Migo, Veronica P.
    Matsumura, Masatoshi
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 231
  • [43] Phosphomolybdic and phosphotungstic acids as efficient catalysts for the synthesis of bridged 1,2,4,5-tetraoxanes from β-diketones and hydrogen peroxide
    Terent'ev, Alexander O.
    Yaremenko, Ivan A.
    Vil', Vera A.
    Moiseev, Igor K.
    Kon'kov, Sergey A.
    Dembitsky, Valery M.
    Levitsky, Dmitri O.
    Nikishin, Gennady I.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2013, 11 (16) : 2613 - 2623
  • [44] The structure and antimalarial activity of dispiro-1,2,4,5-tetraoxanes derived from (+)-dihydrocarvone
    Dong, Yuxiang
    McCullough, Kevin J.
    Wittlin, Sergio
    Chollet, Jacques
    Vennerstrom, Jonathan L.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (22) : 6359 - 6361
  • [45] Comparative antimalarial activities of six pairs of 1,2,4,5-tetraoxanes (peroxide dimers) and 1,2,4,5,7,8-hexaoxonanes (peroxide trimers)
    Dong, Yuxiang
    Creek, Darren
    Chollet, Jacques
    Matile, Hugues
    Charman, Susan A.
    Wittlin, Sergio
    Wood, James K.
    Vennerstrom, Jonathan L.
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (08) : 3033 - 3035
  • [46] SYNTHESIS AND SILICA GEL-CATALYZED DECOMPOSITION OF 3-(1-ARYLCYCLOALKYL)-SUBSTITUTED 1,2,4-TRIOXOLANES AND 1,2,4-DIOXAZOLIDINES
    FUKAGAWA, R
    NOJIMA, M
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1994, (17): : 2449 - 2454
  • [47] MEDI 343-Formation of primary and secondary carbon-centered radicals in the iron (II)-mediated decomposition of antimalarial 1,2,4,5-tetraoxanes
    Dong, Yuxiang
    Vennerstrom, Jonathan L.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2006, 232
  • [48] Design and Discovery of 3,6-Substituted 1,2,4,5-Tetraoxanes as New Class of Falcipain-2 Inhibitors for Antimalarial Action
    Kumawat, Mukesh Kumar
    Singh, Udaya Pratap
    Chetia, Dipak
    PHARMACEUTICAL CHEMISTRY JOURNAL, 2019, 53 (09) : 822 - 830
  • [49] Bridged 1,2,4-Trioxolanes: SnCl4-Catalyzed Synthesis and an In Vitro Study against S. mansoni
    Radulov, Peter S.
    Yaremenko, Ivan A.
    Keiser, Jennifer
    Terent'ev, Alexander O.
    MOLECULES, 2023, 28 (13):
  • [50] Differentiation between 1,2,4,5-tetraoxanes and 1,2,4,5,7,8-hexaoxonanes using 1H and 13C NMR analyses
    Dong, YX
    Vennerstrom, JL
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2001, 38 (02) : 463 - 466