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Russian Chemical Reviews, 2017, Volume 86, Issue 1, Pages 1–17
DOI: https://doi.org/10.1070/RCR4628
(Mi rcr4145)
 

This article is cited in 26 scientific papers (total in 26 papers)

The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis

M. G. Vinogradov, O. V. Turova, S. G. Zlotin

N.D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences
Abstract: The review summarizes data published in the last decade on the reactions of organic compounds involving N-acyliminium ions, including intramolecular arylation (cyclization), cross-coupling with nucleophiles and some other transformations to form new carbon–carbon and carbon–heteroatom bonds. The stereo- and enantioselective versions of these reactions using chiral auxiliaries and asymmetric catalysts (organocatalysts) are considered. Examples of application of N-acyliminium ions for the synthesis of natural compounds and their analogues are presented.
The bibliography includes 100 references.
Funding agency Grant number
Russian Science Foundation 14-50-00126
Received: 22.01.2016
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: M. G. Vinogradov, O. V. Turova, S. G. Zlotin, “The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis”, Russian Chem. Reviews, 86:1 (2017), 1–17
Citation in format AMSBIB
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\by M.~G.~Vinogradov, O.~V.~Turova, S.~G.~Zlotin
\paper The progress in the chemistry of N-acyliminium ions and their use in stereoselective organic synthesis
\jour Russian Chem. Reviews
\yr 2017
\vol 86
\issue 1
\pages 1--17
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\crossref{https://doi.org/10.1070/RCR4628}
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Linking options:
  • https://www.mathnet.ru/eng/rcr4145
  • https://doi.org/10.1070/RCR4628
  • https://www.mathnet.ru/eng/rcr/v86/i1/p1
  • This publication is cited in the following 26 articles:
    1. Yun Zhang, Jia‐Huan Nie, Yao Du, Xin‐Rui Ye, Bao‐Dong Cui, Xue‐Qing Mou, Jia‐Bao Liu, Wei‐Cheng Yuan, Yong‐Zheng Chen, Chemistry — An Asian Journal, 2025  crossref
    2. Jakub Adamek, Wiktoria Kaczmarczyk, Dawid Sapia, Molbank, 2024:2 (2024), M1834  crossref
    3. You-Gui Li, Wei-Ke Chen, You-Qiang Guo, Zhang Zhu, Jing-Jing Cao, Zhen-Yu Wang, Xiang Wu, Tetrahedron Letters, 122 (2023), 154519  crossref
    4. Satish Bhoge, Prabal Pratap Singh, Deepak K. Das, Ranjan Patra, ChemistrySelect, 8:40 (2023)  crossref
    5. O. Grossmann, R. Maji, M. Aukland, S. Lee, B. List, Angew. Chem.-Int. Edit., 61:9 (2022), e202115036  crossref  isi
    6. J. Adamek, M. Grymel, A. Kuźnik, A. Październiok-Holewa, Molecules, 27:5 (2022), 1562  crossref
    7. O. Grossmann, R. Maji, M. H. Aukland, S. Lee, B. List, Angewandte Chemie, 134:9 (2022)  crossref
    8. G. Y. Remennikov, The Alkaloids: Chemistry and Biology, 88, 2022, 49  crossref
    9. Q.-W. Gui, Zh.-Yu. Xiong, F. Teng, T.-Ch. Cai, Q. Li, W. Hu, X. Wang, J. Yu, X. Liu, Org. Biomol. Chem., 19:38 (2021), 8254–8258  crossref  isi
    10. X. Han, X. Nie, Y. Feng, B. Wei, Ch. Si, G. Lin, Chin. Chem. Lett., 32:11 (2021), 3526–3530  crossref  isi
    11. Ch.-Ch. Zhang, Zh.-P. Huo, M.-L. Tang, Y.-X. Liang, X. Sun, Tetrahedron Lett., 68 (2021), 152946  crossref  mathscinet  isi  scopus
    12. E. Le Du, M. Garreau, J. Waser, Chem. Sci., 12:7 (2021), 2467–2473  crossref  isi  scopus
    13. D. Kozicka, P. Zielezny, K. Erfurt, J. Adamek, Catalysts, 11:5 (2021), 552  crossref  isi
    14. V. N. Babu, A. Murugan, N. Katta, S. Devatha, D. S. Sharada, J. Org. Chem., 84:11 (2019), 6631–6641  crossref  isi
    15. D. Seebach, Helv. Chim. Acta, 102:6 (2019), e1900072  crossref  isi
    16. A. A. Fesenko, A. N. Yankov, A. D. Shutalev, Tetrahedron, 75:45 (2019), 130527  crossref  isi  scopus
    17. I. Zaragoza-Galicia, Z. A. Santos-Sanchez, Ya. I. Hidalgo-Mercado, H. F. Olivo, M. Romero-Ortega, Synthesis, 51:24 (2019), 4650–4656  crossref  isi
    18. L. I. Belen'kii, Yu. B. Evdokimenkova, Advances in Heterocyclic Chemistry, Vol 129, Adv. Heterocycl. Chem., Advances in Heterocyclic Chemistry, 129, ed. E. Scriven, C. Ramsden, Elsevier Academic Press Inc, 2019, 337–418  crossref  isi  scopus
    19. V. V. Kouznetsov, C. E. Puerto Galvis, Tetrahedron, 74:8 (2018), 773–810  crossref  isi
    20. J. Adamek, A. Wegrzyk, J. Konczewicz, K. Walczak, K. Erfurt, Molecules, 23:10 (2018), 2453  crossref  isi  scopus
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