Recent Strategies in the Synthesis of Spiroindole and Spirooxindole Scaffolds

被引:0
|
作者
Shima Nasri
Mohammad Bayat
Faezeh Mirzaei
机构
[1] Imam Khomeini International University,Department of Chemistry, Faculty of Science
来源
关键词
Heterocycles; Multicomponent reaction; Spiroindole; Spirooxindole; Spiroheterocycle;
D O I
暂无
中图分类号
学科分类号
摘要
Spiroindole and spirooxindole scaffolds are very important spiro-heterocyclic compounds in drug design processes. Significant attention has been directed at obtaining molecules based on spiroindole and spirooxindole derivatives that have bioactivity against cancer cells, microbes, and different types of disease affecting the human body. Due to their inherent three-dimensional nature and ability to project functionalities in all three dimensions, they have become biological targets. Considering reports on spiroindole and spirooxindole-containing scaffolds in the past decades, introducing novel synthetic procedures has been an active research field of organic chemistry for well over a century and will be useful in creating new therapeutic agents. This review summarizes the pharmacological significance of spiroindole and spirooxindole scaffolds and highlights the latest strategies for their synthesis, focusing particularly on the past 2 years with typical examples. The spiroindole and spirooxindoles in this review are divided by the type and ring size of the spirocycle that is fused to indole or oxindole. Summarizing these procedures will be very beneficial for discovering novel therapeutic candidate molecules.
引用
收藏
相关论文
共 50 条
  • [1] Recent Strategies in the Synthesis of Spiroindole and Spirooxindole Scaffolds
    Nasri, Shima
    Bayat, Mohammad
    Mirzaei, Faezeh
    [J]. TOPICS IN CURRENT CHEMISTRY, 2021, 379 (04)
  • [2] Recent investigations in the synthesis of spirooxindole derivatives by Iranian researchers
    Leila Youseftabar-Miri
    Hamide Hosseinjani-Pirdehi
    Ahmad Akrami
    Sara Hallajian
    [J]. Journal of the Iranian Chemical Society, 2020, 17 : 2179 - 2231
  • [3] Recent investigations in the synthesis of spirooxindole derivatives by Iranian researchers
    Youseftabar-Miri, Leila
    Hosseinjani-Pirdehi, Hamide
    Akrami, Ahmad
    Hallajian, Sara
    [J]. JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2020, 17 (09) : 2179 - 2231
  • [4] An Access to Highly Functionalized Dihydrobenzofuran Spirooxindole Scaffolds
    Wang, Daqian
    Sun, Jing
    Han, Ying
    Sun, Qiu
    Yan, Chao-Guo
    [J]. ORGANIC LETTERS, 2022, : 7790 - 7795
  • [5] Recent Advances and Strategies towards Synthesis of Indolyl and Tryptophan-C-Glycoside Scaffolds
    Sangwan, Rekha
    Azeem, Zanjila
    Kumar Mandal, Pintu
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2024, 366 (07) : 1484 - 1508
  • [6] Synthesis of Zr-MOF/rGO-nanocomposites used for spirooxindole scaffolds derivatives
    Kumar, Gyanendra
    Dutta, Arup
    Goswami, Munmee
    Meena, Bachan
    Parasuboyina, Sreehari
    Nongkhlaw, Rishanlang
    Masram, Dhanraj T.
    [J]. JOURNAL OF MOLECULAR STRUCTURE, 2023, 1287
  • [7] 1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments
    Fatemeh Rostami Miankooshki
    Mohammad Bayat
    Shima Nasri
    Narges Habibi Samet
    [J]. Molecular Diversity, 2023, 27 : 2365 - 2397
  • [8] 1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments
    Miankooshki, Fatemeh Rostami
    Bayat, Mohammad
    Nasri, Shima
    Samet, Narges Habibi
    [J]. MOLECULAR DIVERSITY, 2023, 27 (05) : 2365 - 2397
  • [9] Rhodium-Catalyzed C-H Activation of Indoles for the Construction of Spiroindole Scaffolds
    Wang, Huiying
    Wang, Mengmeng
    Ma, Biao
    Dai, Hui-Xiong
    [J]. SYNTHESIS-STUTTGART, 2022, 54 (21): : 4727 - 4733
  • [10] SYNTHESIS OF SOME SULFUR-CONTAINING SPIROINDOLE DERIVATIVES
    JOSHI, KC
    SHARMA, D
    JOSHI, BS
    [J]. PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS, 1990, 48 (1-4): : 33 - 36