Synthetic strategies for the construction of C3-N1′ bisindoles

被引:0
|
作者
Abe, Takumi [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, 1-1-1 Tsushima Naka,Kita Ku, Okayama 7008530, Japan
基金
日本学术振兴会;
关键词
Positive ions;
D O I
10.1039/d3ob02089d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
C3-N1 ' bisindoles are unique structures, and the construction of these structures has drawn much attention. However, their synthesis still presents significant challenges that limit the functional group compatibility. This minireview summarizes the recent progress in the methodology for constructing C3-N1 ' bisindoles. There are two approaches for access to C3-N1 ' bisindoles: (1) direct approaches including reverse polarity techniques. (2) Stepwise approaches using designed and prefunctionalized substrates enable further functionalization by additional reactions to facilitate access to the target products. I believe that this review will allow its readers to develop novel approaches for the synthesis of C3-N1 ' bisindoles. Natural products having a C3-N1 ' bisindole framework are unique structures with potential axial chirality. This minireview summarizes the recent progress of the methodology for constructing C3-N1 ' bisindoles along with the possible mechanism.
引用
收藏
页码:1756 / 1764
页数:9
相关论文
共 50 条
  • [31] Spongistatin synthetic studies .1. Construction of a C(29-48) subtarget
    Smith, AB
    Zhuang, LH
    Brook, CS
    Boldi, AM
    McBriar, MD
    Moser, WH
    Murase, N
    Nakayama, K
    Verhoest, PR
    Lin, QY
    TETRAHEDRON LETTERS, 1997, 38 (50) : 8667 - 8670
  • [32] A Review on Modern Synthetic Route for the Construction of 1, 3-Diazanaphthalene Moiety
    Faheem, Mohd
    Tiwari, Anjani K.
    Singh, Vinay K.
    CURRENT ORGANIC CHEMISTRY, 2020, 24 (10) : 1108 - 1138
  • [33] Synthetic Studies on Alotamide A: Construction of N-Demethylalotamide A
    Souto, Jose A.
    Roman, David
    Dominguez, Marta
    de Lera, Angel R.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2021, 2021 (44) : 6057 - 6070
  • [34] Synthetic Studies of an Analogue of HIV-1 Protease Inhibitors of Didemnaketals:Construction of the C1-C8 Intermediate
    Ping Zhen WANG
    Yan Xing JIA
    Yong Qiang TU
    Bin WU(Department of Chemistry. National Laboratory of Applied Organic Chemistry
    ChineseChemicalLetters, 1999, (09) : 749 - 750
  • [35] Synthetic studies of an analogue of HIV-1 protease inhibitors of didemnaketals: Construction of the C1-C8 intermediate
    Wang, PZ
    Jia, YX
    Tu, YQ
    Wu, B
    CHINESE CHEMICAL LETTERS, 1999, 10 (09) : 749 - 750
  • [36] Harmonic analysis on SO(n, C)/SO(n-1, C), n ≥ 3
    Secanellas, Sofia Aparicio
    ACTA APPLICANDAE MATHEMATICAE, 2006, 90 (1-2) : 3 - 17
  • [37] Synthetic Strategies Toward N-Functionalized Cyclens
    Suchy, Moimir
    Hudson, Robert H. E.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2008, 2008 (29) : 4847 - 4865
  • [38] The crossing number of C(n; {1, 3})
    Yang, YS
    Lin, XH
    Lu, JG
    Hao, X
    DISCRETE MATHEMATICS, 2004, 289 (1-3) : 107 - 118
  • [39] (+)-sorangicin A synthetic studies. Construction of the C(1-15) and C(16-29) subtargets
    Smith, AB
    Fox, RJ
    Vanecko, JA
    ORGANIC LETTERS, 2005, 7 (14) : 3099 - 3102
  • [40] Phorboxazole B synthetic studies: construction of C(1-32) and C(33-46) subtargets
    Paterson, I
    Steven, A
    Luckhurst, CA
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2004, 2 (20) : 3026 - 3038