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Russian Chemical Reviews, 2020, Volume 89, Issue 5, Pages 537–572
DOI: https://doi.org/10.1070/RCR4910
(Mi rcr4290)
 

This article is cited in 9 scientific papers (total in 9 papers)

Stereochemistry, mechanisms and applications of electrophilic reactions of organophosphorus compounds

O. I. Kolodiazhnyi

Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine, Kyiv
Abstract: The review summarizes and systimatizes data on the stereochemistry, mechanisms and applications of electrophilic reactions of organophosphorus compounds. Asymmetric versions of the Michaelis–Arbuzov, Michaelis–Becker, Hirao, Staudinger, Pudovik and other reactions are considered. Key issues of asymmetric electrophilic catalysis are discussed. The reaction conditions, catalytic systems and structures of the reaction products are presented. Asymmetric electrophilic reactions are used in organic synthesis and in studies of the mechanisms of chemical processes involving organophosphorus compounds.
The bibliography includes 209 references.
Received: 11.07.2019
Bibliographic databases:
Document Type: Article
Language: English
Original paper language: Russian
Citation: O. I. Kolodiazhnyi, “Stereochemistry, mechanisms and applications of electrophilic reactions of organophosphorus compounds”, Russian Chem. Reviews, 89:5 (2020), 537–572
Citation in format AMSBIB
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\by O.~I.~Kolodiazhnyi
\paper Stereochemistry, mechanisms and applications of electrophilic reactions of organophosphorus compounds
\jour Russian Chem. Reviews
\yr 2020
\vol 89
\issue 5
\pages 537--572
\mathnet{http://mi.mathnet.ru/eng/rcr4290}
\crossref{https://doi.org/10.1070/RCR4910}
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Linking options:
  • https://www.mathnet.ru/eng/rcr4290
  • https://doi.org/10.1070/RCR4910
  • https://www.mathnet.ru/eng/rcr/v89/i5/p537
  • This publication is cited in the following 9 articles:
    1. Goutam Brahmachari, Visible Light-Driven Organic Synthesis, 2025, 221  crossref
    2. Goutam Brahmachari, Organophosphorus Chemistry, 2024, 287  crossref
    3. A. Jaillet, J. Bayardon, Y. Rousselin, S. Jugé, J. Org. Chem., 88:24 (2023), 16679  crossref
    4. E. V. Shishkin, O. V. Anishchenko, M. A. Shevchenko, Yu. L. Zotov, A. V. Cherikov, Russ. J. Gen. Chem., 93:S1 (2023), S256  crossref
    5. P. M. Sansores Peraza, J. Garcia Lopez, Y. Navarro, M. J. Iglesias, F. Lopez Ortiz, Synthesis, 54:03 (2022), 600–616  crossref  isi
    6. O. Kolodiazhnyi, A. Kolodiazhna, E. Grishkun, D. Prysiazhnuk, O. Kolodiazhna, S. Sheiko, Phosphorus Sulfur Silicon Relat. Elem., 197:5-6 (2022), 474–479  crossref  isi
    7. I. R. Dayanova, A. V. Kurenkov, K. D. Akhmadgaleev, K. R. Trigulova, D. R. Islamov, O. E. Naumova, I. D. Strelnik, E. I. Musina, A. A. Karasik, Mendeleev Communications, 32:5 (2022), 622  crossref
    8. Goutam Brahmachari, Organophosphorus Chemistry, 2022, 398  crossref
    9. Yu. I. Blokhin, I. A. Lyubimov, A. M. Bagautdinov, D. K. Gaykov, Russ. Chem. Bull., 70:10 (2021), 2041–2043  crossref  isi  scopus
    Citing articles in Google Scholar: Russian citations, English citations
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