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Russian Chemical Reviews, 1967, Volume 36, Issue 10, Pages 753–771
DOI: https://doi.org/10.1070/RC1967v036n10ABEH001769
(Mi rcr2122)
 

This article is cited in 33 scientific papers (total in 33 papers)

Synthesis of substituted indoles via indolines

M. N. Preobrazhenskaya

All-Union Scientific Research Chemical-Pharmaceutical Institute, Moscow
Abstract: CONTENTS
I. Introduction 753
II. Methods of preparation of indolines 754
III. Introduction of substituents into the benzene ring of the indoline molecule 758
IV. Introduction of substituents into the pyrrole ring of the indoline molecule 763
V. Conversion of indoline derivatives into indoles 764
Document Type: Article
UDC: 547.751:747.753
Language: English
Original paper language: Russian


Citation: M. N. Preobrazhenskaya, “Synthesis of substituted indoles via indolines”, Usp. Khim., 36:10 (1967), 1760–1798; Russian Chem. Reviews, 36:10 (1967), 753–771
Linking options:
  • https://www.mathnet.ru/eng/rcr2122
  • https://doi.org/10.1070/RC1967v036n10ABEH001769
  • https://www.mathnet.ru/eng/rcr/v36/i10/p1760
  • This publication is cited in the following 33 articles:
    1. Stepan K. Krymov, Alexander M. Scherbakov, Lyubov G. Dezhenkova, Diana I. Salnikova, Svetlana E. Solov'eva, Danila V. Sorokin, Daniela Vullo, Viviana De Luca, Clemente Capasso, Claudiu T. Supuran, Andrey E. Shchekotikhin, Pharmaceuticals, 15:12 (2022), 1453  crossref
    2. Xueyou Tan, Xiaohui Wu, Ziqi Hu, Ding Ma, Zujin Shi, RSC Adv., 7:48 (2017), 29985  crossref
    3. Vigorov A.Yu., Nizova I.A., Shalunova K.E., Grishakov A.N., Sadretdinova L.Sh., Ganebnykh I.N., Ezhikova M.A., Kodess M.I., Krasnov V.P., Russ. Chem. Bull., 60:5 (2011), 873–881  crossref  isi
    4. Hojat Veisi, Ramin Ghorbani-Vaghei, Tetrahedron, 66:38 (2010), 7445  crossref
    5. M. A. Yurovskaya, Chem Heterocycl Compd, 41:1 (2005), 24  crossref
    6. Barry B. Snider, Hongbo Zeng, J. Org. Chem., 68:2 (2003), 545  crossref
    7. Takayoshi Hara, Kohsuke Mori, Tomoo Mizugaki, Kohki Ebitani, Kiyotomi Kaneda, Tetrahedron Letters, 44:33 (2003), 6207  crossref
    8. Ulf Tilstam, Michael Harre, Thilo Heckrodt, Hilmar Weinmann, Tetrahedron Letters, 42:32 (2001), 5385  crossref
    9. John D. Chisholm, David L. Van Vranken, J. Org. Chem., 65:22 (2000), 7541  crossref
    10. Barry B. Snider, Hongbo Zeng, Org. Lett., 2:25 (2000), 4103  crossref
    11. Feng He, Bruce M. Foxman, Barry B. Snider, J. Am. Chem. Soc., 120:25 (1998), 6417  crossref
    12. R.J. Sundberg, Indoles, 1996, 145  crossref
    13. Comprehensive Heterocyclic Chemistry II, 1996, 969  crossref
    14. Richard J. Sundberg, Comprehensive Heterocyclic Chemistry II, 1996, 119  crossref
    15. William F. Bailey, Xing-Long Jiang, J. Org. Chem., 61:8 (1996), 2596  crossref
    16. Maria N. Preobrazhenskaya, Ilya A. Korbukh, Chemistry of Nucleosides and Nucleotides, 1994, 1  crossref
    17. S. L. Vorob'eva, V. N. Buyanov, N. N. Suvorov, Chem Heterocycl Compd, 27:5 (1991), 506  crossref
    18. Ehud Keinan, Noam Greenspoon, Comprehensive Organic Synthesis, 1991, 523  crossref
    19. Daniel M. Ketcha, Tetrahedron Letters, 29:18 (1988), 2151  crossref
    20. A. E. Zelenin, N. D. Chkanikov, A. F. Kolomiets, A. V. Fokin, Russ Chem Bull, 37:1 (1988), 110  crossref
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