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Mendeleev Communications, 1992, Volume 2, Issue 3, Pages 106–108
DOI: https://doi.org/10.1070/MC1992v002n03ABEH000157
(Mi mendc5428)
 

This article is cited in 19 scientific papers (total in 19 papers)

Phosphorylated Resorcinol-based Cyclophanes

L. N. Markovsky, V. I. Kalchenko, D. M. Rudkevich, A. N. Shivanyuk

Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev, Ukraine
Abstract: Complete and partial O-functionalization of the octahydroxytetramethyl[14]metacyclophane with phosphoryl groups has been carried out, arid reversible intramolecular addition of hydroxy or trimethylsilyloxy groups to the neighbouring P=O bonds with the formation of spirophosphorane fragments has been shown to be typical of the 3,10,17,24-tetrahydroxy(tetrakistrimethylsilbxy)-5,12,19,26-tetrakis-o-phenylenephosphoryloxy-1,8,15,22-tetramethyl [14]metacyclophane.
Document Type: Article
Language: English


Citation: L. N. Markovsky, V. I. Kalchenko, D. M. Rudkevich, A. N. Shivanyuk, “Phosphorylated Resorcinol-based Cyclophanes”, Mendeleev Commun., 2:3 (1992), 106–108
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  • https://www.mathnet.ru/eng/mendc/v2/i3/p106
  • This publication is cited in the following 19 articles:
    1. Pawan Kumar, V. B. Raja Mani Kandan, Prabukumar Balakrishnan, P. K. Sudhadevi Antharjanam, Venkatakrishnan Parthasarathy, “Leveraging Torsional and Steric Strains: A Pre‐macrocyclization Strategy Enables Conformation‐Specific Fullerene Binding in m‐Cyclophanes”, Angewandte Chemie, 135:41 (2023)  crossref
    2. Pawan Kumar, V. B. Raja Mani Kandan, Prabukumar Balakrishnan, P. K. Sudhadevi Antharjanam, Venkatakrishnan Parthasarathy, “Leveraging Torsional and Steric Strains: A Pre‐macrocyclization Strategy Enables Conformation‐Specific Fullerene Binding in m‐Cyclophanes”, Angew Chem Int Ed, 62:41 (2023)  crossref
    3. Jordan N. Smith, Thomasin K. Brind, Simon B. Petrie, Mikaela S. Grant, Nigel T. Lucas, “One-Step Synthesis of C2v-Symmetric Resorcin[4]arene Tetraethers”, J. Org. Chem., 85:6 (2020), 4574  crossref
    4. Anthony Wishard, Bruce C. Gibb, Calixarenes and Beyond, 2016, 195  crossref
    5. I. S. Nizamov, R. R. Shamilov, G. R. Sabirzyanova, E. I. Nikitin, A. R. Burilov, M. A. Pudovik, “Borylation of calix[4]resorcinols under ultrasonic irradiation”, Russ J Gen Chem, 82:5 (2012), 859  crossref
    6. I. S. Nizamov, L. A. Al'metkina, E. N. Nikitin, G. R. Sabirzyanova, A. R. Burilov, M. A. Pudovik, “Thiophosphorylation of calix[4]resorcinarenes with 2,4-diaryl-1,3-dithia-2λ5,4λ5-diphosphetane 2,4-disulfides”, Russ J Org Chem, 47:10 (2011), 1504  crossref
    7. Volker Böhmer, Patai's Chemistry of Functional Groups, 2009  crossref
    8. Myroslav Vysotsky, Christian Schmidt, Volker Böhmer, Advances in Supramolecular Chemistry, 7, 2000, 139  crossref
    9. I. S. Antipin, E. Kh. Kazakova, W. D. Habicher, A. I. Konovalov, “Phosphorus-containing calixarenes”, Russian Chem. Reviews, 67:11 (1998), 905–922  mathnet  mathnet  crossref  isi  scopus
    10. Peter Timmerman, Willem Verboom, David N. Reinhoudt, “Resorcinarenes”, Tetrahedron, 52:8 (1996), 2663  crossref
    11. Vera I. Maslennikova, Elena V. Panina, Anna R. Bekker, Larisa K. Vasyanina, Eduard E. Nifantyev, “AMIDOPHOSPHITES IN THE CHEMISTRY OF CALYX[4]RESORCINOLARENE”, Phosphorus, Sulfur, and Silicon and the Related Elements, 113:1-4 (1996), 219  crossref
    12. E. Kh. Kazakova, A. I. Konovalov, L. V. Snegur, V. N. Babin, Yu. S. Nekrasov, M. A. Pudovik, “Interaction of resorcinol–octanal cyclotetramer with bis(N,N-diethylamido)menthylphosphite”, Mendeleev Commun., 6:4 (1996), 157–159  mathnet  crossref
    13. Pascale Delangle, Jean-Pierre Dutasta, “Tetraphosphonate-calix[4]resorcinarene. A powerful host for alkali metal and ammonium cations encapsulation.”, Tetrahedron Letters, 36:51 (1995), 9325  crossref
    14. Volker Böhmer, “Calixarene – Makrocyclen mit (fast) unbegrenzten Möglichkeiten”, Angewandte Chemie, 107:7 (1995), 785  crossref
    15. Volker Böhmer, “Calixarenes, Macrocycles with (Almost) Unlimited Possibilities”, Angew. Chem. Int. Ed. Engl., 34:7 (1995), 713  crossref
    16. Oleg Aleksiuk, Flavio Grynszpan, Silvio E. Biali, Calixarenes 50th Anniversary: Commemorative Issue, 1994, 237  crossref
    17. Hans Dressler, Resorcinol, 1994, 437  crossref
    18. Volker B�hmer, Dagmar Kraft, Moniralsadat Tabatabai, “Inherently chiral calixarenes”, J Incl Phenom Macrocycl Chem, 19:1-4 (1994), 17  crossref
    19. Moniralsadat Tabatabai, Walter Vogt, Volker Böhmer, George Ferguson, Erich F. Paulus, “A resorcinol derived calix[5]arene with C5-symmetry”, Supramolecular Chemistry, 4:2 (1994), 147  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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