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Usp. Khim., 2011, Volume 80, Issue 1, Pages 77–106 (Mi rcr39)  

This article is cited in 52 scientific papers (total in 52 papers)

Chemistry of calix[4]resorcinarenes

V. K. Jain, P. H. Kanaiya

School of Sciences, Gujarat University

Abstract: The review demonstrates the progress in the chemistry of calix[4]resorcinarenes over the last decade. Special attention is paid to their synthesis, conformational behaviour, functionalization and ability to serve as cavitands and capsules, to form monolayers and host–guest complexes. Practical applications of calix[4]resorcinarenes and their derivatives in various fields are surveyed.

Full text: http://www.uspkhim.ru/.../paper_rus.phtml?journal_id=rc&paper_id=4127

English version:
Russian Chemical Reviews, 2011, 80:1, 75–102

Bibliographic databases:

Document Type: Article
Received: 15.12.2009

Citation: V. K. Jain, P. H. Kanaiya, “Chemistry of calix[4]resorcinarenes”, Usp. Khim., 80:1 (2011), 77–106; Russian Chem. Reviews, 80:1 (2011), 75–102

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    Citing articles on Google Scholar: Russian citations, English citations
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    This publication is cited in the following articles:
    1. V. K. Jain, P. H. Kanaiya, “ChemInform Abstract: Chemistry of Calix[4]resorcinarenes”, ChemInform, 42:37 (2011), no  crossref
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    3. Julia E. Bartenstein, Nigel T. Lucas, “Reduced symmetry triflate-resorcin[4]arenes”, Supramolecular Chemistry, 2012, 1  crossref  adsnasa  isi  scopus
    4. Jiménez-Gutiérrez I. Eddy, Sánchez-Montes K. Erika, Cortez-Maya Sandra, Flores-Rojas Gabriel, Martínez-García Marcos, “Synthesis of Soluble Carcerands”, MRS Proc, 1371 (2012)  crossref  scopus
    5. Liliya I. Vagapova, Aliya F. Fahertdinov, Alexander R. Burilov, Mikhail A. Pudovik, “Synthesis of New calix[4]resorcinols with [N-diethoxyphosphorylmethyl-N-(2,2-dimethoxyethyl)amino]methyl Substituents at the Upper Rim”, Mendeleev Communications, 22:6 (2012), 325  crossref  isi  scopus
    6. Matthew Partridge, Frank Davis, Steve W. James, Ralph P. Tatam, Charl F.J. Faul, Séamus P.J. Higson, “Monolayer behaviour of calix-4-resorcinarenes and their surfactant complexes”, Thin Solid Films, 2012  crossref  isi  scopus
    7. Svetlana V. Shishkina, Andriy Tarnovskiy, Vladimir Rozhkov, Oleg V. Shishkin, Oleg Lukin, Alexander Shivanyuk, “Binding Properties and Self-Assembly of C2V-Symmetrical Resorcin[4]arene Tetrabenzoates”, Tetrahedron, 2012  crossref  isi  scopus
    8. S. N. Podyachev, T. A. Barsukova, S. V. Bukharov, V. V. Syakaev, S. N. Sudakova, G. N. Nugumanova, A. I. Konovalov, “Synthesis of hydrazones containing sterically hindered phenol groups and tetrathiacalix[4]arene fragment”, Russ J Org Chem, 48:10 (2012), 1360  crossref  isi  elib  scopus
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    11. Fraschetti C., Letzel M.C., Filippi A., Speranza M., Mattay J., “Enantioselective Supramolecular Devices in the Gas Phase. Resorcin[4] Arene as a Model System”, Beilstein J. Org. Chem., 8 (2012), 539–550  crossref  isi  elib  scopus
    12. Knyazeva I.R., Sokolova V.I., Burilov A.R., Pudovik M.A., Dobrynin A.B., Kataeva O.N., Sinyashin O.G., “New Triamidophosphonium Acetals and their Condensation with Resorcinol and its Derivatives”, Russ. Chem. Bull., 61:3 (2012), 631–637  crossref  isi  elib  scopus
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    18. Konczyk J., Kozlowski C., Walkowiak W., “Lead(II) Removal From Aqueous Solutions by Solvent Extraction with Tetracarboxylresorcin[4]Arene”, Physicochem. Probl. Mineral Pro., 49:1 (2013), 213–222  crossref  isi  elib  scopus
    19. Vagapova L.I., Chachkov D.V., Ankushina M.V., Burilov A.R., Pudovik M.A., “Calix[4]Resorcinols Bearing Gamma-Aminoacetal Groups on the Upper Rim. Synthesis and Properties”, Russ. J. Gen. Chem., 83:2 (2013), 319–324  crossref  isi  elib  scopus
    20. Belen'kii L.I. Evdokimenkova Yu.B., “The Literature of Heterocyclic Chemistry, Part XII, 2010-2011”, Advances in Heterocyclic Chemistry, Vol 111, Adv. Heterocycl. Chem., 111, ed. Katritzky A., 2014, 147–274  crossref  isi  scopus
    21. L.I.. Vagapova, A.R.. Burilov, J.K.. Voronina, V.V.. Syakaev, D.R.. Sharafutdinova, “Phosphorylated Aminoacetal in the Synthesis of New Acyclic, Cyclic, and Heterocyclic Polyphenol Structures”, Heteroatom Chem, 2014, n/a  crossref  isi  scopus
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    23. Micke Lisbjerg, B.E.. Nielsen, B.O.. Milhøj, S.P.. A. Sauer, Michael Pittelkow, “Anion binding by biotin[6]uril in water”, Org. Biomol. Chem, 13:2 (2014), 369  crossref  isi  scopus
    24. Vagapova L.I. Burilov A.R. Voronina J.K. Syakaev V.V. Sharafutdinova D.R. Amirova L.R. Pudovik M.A. Garifzyanov A.R. Sinyashin O.G., “Synthesis of 1,3,4-Oxadiazole-Based Aromatic and Heterocyclic/Phenylpyrazole Derivatives”, Heteroatom Chem., 25:3 (2014), 178–185  crossref  isi  elib  scopus
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    27. L. I. Vagapova, A. G. Fakhertdinova, A. R. Burilov, M. A. Pudovik, “Calix[4]resorcinols modified with γ-aminobutyric acid fragments”, Russ J Gen Chem, 85:7 (2015), 1783  crossref  isi  elib  scopus
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    47. Geng W.-Ch., Sun H., Guo D.-Sh., “Macrocycles Containing Azo Groups: Recognition, Assembly and Application”, J. Incl. Phenom. Macrocycl. Chem., 92:1-2 (2018), 1–79  crossref  isi  scopus
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    51. Ribeiro A.C.F., Esteso M.A., “Transport Properties For Pharmaceutical Controlled-Release Systems: a Brief Review of the Importance of Their Study in Biological Systems”, Biomolecules, 8:4 (2018), 178  crossref  isi
    52. Padnya P.L., Potrekeeva O.S., Bayarashov E.E., Stoikov I.I., “Spatial Structure of Tetrasubstituted Thiacalix[4]Arenes Containing l-Tryptophan Fragments in Solution”, Russ. J. Gen. Chem., 88:11 (2018), 2328–2334  crossref  isi
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