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Russian Chemical Reviews, 1994, Volume 63, Issue 7, Pages 575–609
DOI: https://doi.org/10.1070/RC1994v063n07ABEH000106
(Mi rcr1182)
 

This article is cited in 17 scientific papers (total in 17 papers)

Trivalent phosphorus acids amides as phosphorylating agents for alcohols and amines

E. E. Nifantyev, M. K. Grachev

Department of Chemistry, Moscow State Pedagogical University
Abstract: The principal results of studies on trivalent phosphorus acid amides (TPAA) as phosphorylating agents for alcohols, phenols, and amines are summarised and discussed. Problems concerning the catalysis and mechanism of the phosphorylation of proton-donating nucleophiles by TPAA are considered and new possibilities for the development of investigations on these lines are analysed. The preparative advantages of TPAA and the specific prospects for their use in fine organic synthesis and macromolecular chemistry are demonstrated. The bibliography includes 560 references.
Received: 23.05.1994
Bibliographic databases:
Document Type: Article
UDC: 547.953+547.91
Language: English
Original paper language: Russian


Citation: E. E. Nifantyev, M. K. Grachev, “Trivalent phosphorus acids amides as phosphorylating agents for alcohols and amines”, Usp. Khim., 63:7 (1994), 602–637; Russian Chem. Reviews, 63:7 (1994), 575–609
Linking options:
  • https://www.mathnet.ru/eng/rcr1182
  • https://doi.org/10.1070/RC1994v063n07ABEH000106
  • https://www.mathnet.ru/eng/rcr/v63/i7/p602
  • This publication is cited in the following 17 articles:
    1. K. N. Kornilov, Phosphorus, Sulfur, and Silicon and the Related Elements, 193:8 (2018), 484  crossref
    2. Blokhin Yu.I. Kornilov K.N. Akilin A.V. Abramov I.A. Bagautdinov A.M. Lyubimov I.A., Russ. Chem. Bull., 65:4 (2016), 910–922  crossref  isi
    3. M. G. Pervova, K. A. Plotnikova, D. L. Chizhov, A. V. Pestov, V. I. Saloutin, J Anal Chem, 71:6 (2016), 630  crossref
    4. M. K. Grachev, Russian Chem. Reviews, 82:11 (2013), 1034–1046  mathnet  mathnet  crossref  isi  scopus
    5. Laurent Lefort, Johannes G. de Vries, Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis, 2012, 133  crossref
    6. Vasile Simulescu, Gheorghe Ilia, J Incl Phenom Macrocycl Chem, 66:1-2 (2010), 3  crossref
    7. Erkki Nurminen, Harri Lönnberg, J of Physical Organic Chem, 17:1 (2004), 1  crossref
    8. Shinya Mizuta, Mikito Sadamori, Tetsuya Fujimoto, Iwao Yamamoto, Angewandte Chemie, 115:29 (2003), 3505  crossref
    9. Shinya Mizuta, Mikito Sadamori, Tetsuya Fujimoto, Iwao Yamamoto, Angew Chem Int Ed, 42:29 (2003), 3383  crossref
    10. Erkki. J. Nurminen, Jorma K. Mattinen, Harri Lönnberg, Helvetica Chimica Acta, 86:6 (2003), 2005  crossref
    11. Anatoliy S. Bushnev, Dennis C. Liotta, Methods in Enzymology, 311, Sphingolipid Metabolism and Cell Signaling Part A, 2000, 535  crossref
    12. I. S. Antipin, E. Kh. Kazakova, W. D. Habicher, A. I. Konovalov, Russian Chem. Reviews, 67:11 (1998), 905–922  mathnet  mathnet  crossref  isi  scopus
    13. Edward E. Nifantyev, Mikhail K. Gratchev, Vera Yu. Mishina, Il'Dar G. Mustafin, Phosphorus, Sulfur, and Silicon and the Related Elements, 130:1 (1997), 35  crossref
    14. Cyrille Loeber, Dominique Matt, Pierrette Briard, Daniel Grandjean, J. Chem. Soc., Dalton Trans., 1996, no. 4, 513  crossref
    15. Oleg I. Kolodiazhnyi, Evgen V. Grishkun, Tetrahedron: Asymmetry, 7:4 (1996), 967  crossref
    16. Vera I. Maslennikova, Elena V. Panina, Anna R. Bekker, Larisa K. Vasyanina, Eduard E. Nifantyev, Phosphorus, Sulfur, and Silicon and the Related Elements, 113:1-4 (1996), 219  crossref
    17. E. E. Nifantyev, M. K. Grachev, Russian Chem. Reviews, 63:7 (1994), 575–609  mathnet  mathnet  crossref  isi  scopus
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