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Russian Chemical Reviews, 2018, Volume 87, Issue 2, Pages 167–191
DOI: https://doi.org/10.1070/RCR4782
(Mi rcr4200)
 

This article is cited in 43 scientific papers (total in 43 papers)

Methods for the synthesis of O-, S- and N-vinyl derivatives

M. S. Ledovskaya, V. V. Voronin, K. S. Rodygin

Saint Petersburg State University
Abstract: The currently known methods for the preparation of vinyl ethers, vinyl sulfides and enamines are analyzed and described systematically. The published data on the reactions of alcohols, thiols and various nitrogen-containing compounds with acetylene, resulting in the corresponding vinyl derivatives, are considered. The attention is focused on the application of convenient acetylene sources. Other modern approaches to the synthesis of vinyl derivatives are described in detail, including vinyl exchange and metathesis reactions, various types of cross-coupling and cleavage of organic compounds. Some specific synthetic routes to vinyl ethers, vinyl sulfides and enamines are presented in the last Section.
The bibliography includes 262 references.
Funding agency Grant number
Russian Science Foundation 16-13-10301
Received: 06.09.2017
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: M. S. Ledovskaya, V. V. Voronin, K. S. Rodygin, “Methods for the synthesis of O-, S- and N-vinyl derivatives”, Russian Chem. Reviews, 87:2 (2018), 167–191
Citation in format AMSBIB
\Bibitem{LedVorRod18}
\by M.~S.~Ledovskaya, V.~V.~Voronin, K.~S.~Rodygin
\paper Methods for the synthesis of $\mathrm{O}$-, $\mathrm{S}$- and $\mathrm{N}$-vinyl derivatives
\jour Russian Chem. Reviews
\yr 2018
\vol 87
\issue 2
\pages 167--191
\mathnet{http://mi.mathnet.ru/eng/rcr4200}
\crossref{https://doi.org/10.1070/RCR4782}
\adsnasa{https://adsabs.harvard.edu/cgi-bin/bib_query?2018RuCRv..87..167L}
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Linking options:
  • https://www.mathnet.ru/eng/rcr4200
  • https://doi.org/10.1070/RCR4782
  • https://www.mathnet.ru/eng/rcr/v87/i2/p167
  • This publication is cited in the following 43 articles:
    1. Maria S. Ledovskaya, Vladimir V. Voronin, Anna A. Reznichenko, Ekaterina A. Reznichenko, Organics, 6:1 (2025), 5  crossref
    2. Heba H. Mohamedy, Monday Peter Ajisafe, Eman Fayad, Matokah Abualnaja, Arwa sultan Alqahtani, Hua-Li Qin, New J. Chem., 2025  crossref
    3. Zhong‐Tao Jiang, Zhengzhao Chen, Ying Xia, Angewandte Chemie, 136:11 (2024)  crossref
    4. Zhong‐Tao Jiang, Zhengzhao Chen, Ying Xia, Angew Chem Int Ed, 63:11 (2024)  crossref
    5. Chloe L. Johnson, Daniel J. Storm, M. Arif Sajjad, Matthew R. Gyton, Simon B. Duckett, Stuart A. Macgregor, Andrew S. Weller, Miquel Navarro, Jesús Campos, Angew Chem Int Ed, 63:30 (2024)  crossref
    6. L. Anders Hammarback, Tania Medina-Gil, Anna Sadurní, Antonio M. Echavarren, Org. Lett., 2024  crossref
    7. Chloe G. Williams, Sepand K. Nistanaki, Krista Dong, Woojin Lee, Kendall N. Houk, Hosea M. Nelson, Org. Lett., 26:23 (2024), 4847  crossref
    8. Saša Opačak, Sergey Tin, Adv Synth Catal, 2024  crossref
    9. Chloe L. Johnson, Daniel J. Storm, M. Arif Sajjad, Matthew R. Gyton, Simon B. Duckett, Stuart A. Macgregor, Andrew S. Weller, Miquel Navarro, Jesús Campos, Angewandte Chemie, 136:30 (2024)  crossref
    10. M. S. Ledovskaya, V. V. Voronin, Russ J Gen Chem, 94:11 (2024), 2833  crossref
    11. V. V. Voronin, M. S. Ledovskaya, Russ J Gen Chem, 94:12 (2024), 3155  crossref
    12. Shiwei Lü, Zipeng Wang, Xiang Gao, Kai Chen, Shifa Zhu, Angewandte Chemie, 135:16 (2023)  crossref
    13. Shiwei Lü, Zipeng Wang, Xiang Gao, Kai Chen, Shifa Zhu, Angewandte Chemie International Edition, 62:16 (2023)  crossref
    14. M. S. Ledovskaya, V. V. Voronin, Tetrahedron, 149 (2023), 133720  crossref
    15. V. V. Voronin, M. V. Polynski, M. S. Ledovskaya, Chemistry — An Asian Journal, 18:23 (2023)  crossref
    16. M. S. Ledovskaya, V. V. Voronin, N. R. Valov, Russ J Gen Chem, 93:2 (2023), 235  crossref  crossref
    17. N. Mukherjee, T. Chatterjee, Green Chem., 25:21 (2023), 8798  crossref
    18. T. Medina-Gil, A. Sadurní, L. A. Hammarback, A. M. Echavarren, ACS Catal., 13:16 (2023), 10751  crossref
    19. A. Domzalska-Pieczykolan, I. Funes-Ardoiz, B. Furman, C. Bolm, Angew. Chem.-Int. Edit., 61:1 (2022), e202109801  crossref  isi  scopus
    20. Tairan Cheng, Boxiang Liu, Rui Wu, Shifa Zhu, Chem. Sci., 13:25 (2022), 7604  crossref
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