HYDROXYLATION OF INDOLE-3-CARBOXYLIC ACID

被引:0
|
作者
MARCHELLI, R
HUTZINGER, O
HEACOCK, RA
机构
来源
PHARMACEUTICA ACTA HELVETIAE | 1971年 / 46卷 / 03期
关键词
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
引用
收藏
页码:150 / +
页数:1
相关论文
共 50 条
  • [41] COORDINATION OF METAL-IONS BY INDOLIC ACIDS - COPPER(II) COMPLEXES OF INDOLE-3-CARBOXYLIC, INDOLE-5-CARBOXYLIC, INDOLE-N-ACETIC, AND N-METHYLINDOLE-2-CARBOXYLIC ACIDS
    ERRE, LS
    MICERA, G
    PIU, P
    PUSINO, A
    CARIATI, F
    JOURNAL OF COORDINATION CHEMISTRY, 1986, 14 (03) : 209 - 214
  • [42] Gold(III)-Catalyzed Decarboxylative C3-Benzylation of Indole-3-carboxylic Acids with Benzylic Alcohols in Water
    Hikawa, Hidemasa
    Kotaki, Fumiya
    Kikkawa, Shoko
    Azumaya, Isao
    JOURNAL OF ORGANIC CHEMISTRY, 2019, 84 (04): : 1972 - 1979
  • [43] Synthesis of 2-(2,2-dimethyl-1-oxopropyl)-indole-3-carboxylic acid by the indoledione-indole rearrangement method in NaOH/AQ. DMSO
    Rekhter M.A.
    Rekhter B.A.
    Yazlovetskii I.G.
    Panasenko A.A.
    Chemistry of Heterocyclic Compounds, 1998, 34 (2) : 250 - 251
  • [44] Heterocyclic Analogs of 5,12-Naphthacenequinone 14*. Synthesis of naphtho[2,3-f]indole-3-carboxylic Acid Derivatives
    Tikhomirov, Alexander S.
    Litvinova, Valeriya A.
    Luzikov, Yury N.
    Korolev, Alexander M.
    Sinkevich, Yuri B.
    Shchekotikhin, Andrey E.
    CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2017, 53 (10) : 1072 - 1079
  • [45] Indole-3-Carboxylic Acid From the Endophytic Fungus Lasiodiplodia pseudotheobromae LPS-1 as a Synergist Enhancing the Antagonism of Jasmonic Acid Against Blumeria graminis on Wheat
    Que, Yawei
    Huang, Donghai
    Gong, Shuangjun
    Zhang, Xuejiang
    Yuan, Bin
    Xue, Minfeng
    Shi, Wenqi
    Zeng, Fansong
    Liu, Meilin
    Chen, Tingting
    Yu, Dazhao
    Yan, Xia
    Wang, Zhengyi
    Yang, Lijun
    Xiang, Libo
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2022, 12
  • [46] Heterocyclic Analogs of 5,12-Naphthacenequinone 14*. Synthesis of naphtho[2,3-f]indole-3-carboxylic Acid Derivatives
    Alexander S. Tikhomirov
    Valeriya A. Litvinova
    Yury N. Luzikov
    Alexander M. Korolev
    Yuri B. Sinkevich
    Andrey E. Shchekotikhin
    Chemistry of Heterocyclic Compounds, 2017, 53 : 1072 - 1079
  • [47] Electrochemical Determination of Indole-3-carboxylic Acid Using Carboxyl Functionalized Multi-Walled Carbon Nanotubes Modified Glassy Carbon Electrode
    Jia, X. L.
    Ye, J. H.
    Wang, F. Q.
    Hu, Y. L.
    Zheng, M. Z.
    Wu, C. Z.
    INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE, 2018, 13 (09): : 8530 - 8542
  • [48] Expression of Toll-like Receptor Genes and Antiviral Cytokines in Macrophage-like Cells in Response to Indole-3-carboxylic Acid Derivative
    Narovlyansky, Alexander
    Pronin, Alexander
    Poloskov, Vladislav
    Sanin, Alexander
    Mezentseva, Marina
    Fedyakina, Irina
    Suetina, Irina
    Zubashev, Igor
    Ershov, Felix
    Filimonova, Marina
    Surinova, Valentina
    Volkova, Irina
    Bogdanov, Egor
    VIRUSES-BASEL, 2024, 16 (11):
  • [49] Synthesis of 2-(2,2-dimethyl-1-oxopropyl)indole-3-carboxylic acid by indoledione-indole rearrangement in aqueous DMSO-NaOH medium
    Rekhter, MA
    Rekhter, BA
    Yazlovetsky, IG
    Panasenko, AA
    KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII, 1998, (02): : 276 - 277
  • [50] BIOGENESIS OF ASCORBIGEN, 3-INDOLYLACETONITRILE AND INDOLE-3-CARBOXYLIC ACID FROM D,L-TRYPTOPHAN-3-C-14 IN BRASSICA-OLERACEA L
    KUTACEK, M
    PROCHAZKA, Z
    GRUNBERGER, D
    NATURE, 1960, 187 (4731) : 61 - 62