Mono-, 1,3-Di- and tetrasubstituted p-tert-butylthiacalix[4]arenes containing phthalimide groups: Synthesis and functionalization with ester, amide, hydrazide and amino groups

Macroheterocycles

Volumn 5, Issue 3, 2012, Pages 266-274

  Galukhin, Andrey V ^a   Zaikov, Evgeny N ^a   Antipin, Igor S ^a   Konovalov, Alexander I ^a   Stoikov, Ivan I ^a,b  

^a KAZAN FEDERAL UNIVERSITY   (Russian Federation)

^b KAZAN INSTITUTE OF BIOCHEMISTRY AND BIOPHYSICS   (Russian Federation)

Author keywords

Phthalimide group; Picrate extraction; Recognition of cations; Thiacalix 4 arene

Indexed keywords

EID: 84922686656     PISSN: 19989539     EISSN: None     Source Type: Journal    
DOI: 10.6060/mhc2012.120781s     Document Type: Article

References (21)

1. Atwood J.L., Steed J.W. Organic Nanostructures. Weinheim: Wiley-VCH, 2008. 352 p.
2. Gutsche CD. Calixarenes - An Introduction, 2nd Edition. Cambridge: RSC, 2008. 290 p.
3. Iki N., Miyano S. J. Inclusion Phenom. Macrocyclic Chem. 2001, 41, 99-105.
4. Lhotak P. Eur. J. Org. Chem. 2004, 71, 1675-1692.
5. Morohashi N., Narumi F., Iki N., Hattori T., Miyano S. Chem. Rev. 2006, 106, 5291-5316.
6. Bhalla V., Kumar M., Hattori T., Miyano S. Tetrahedron 2004, 60, 5881-5887.
7. Bitter I., Csokai V. Tetrahedron Lett. 2003, 44, 2261-2265.
8. Bhalla V., Babu N., Kumar M., Hattori T., Miyano S. Tetrahedron Lett. 2007, 48, 1581-1585.
9. Kumar M., Dhir A., Bhalla V. Tetrahedron 2009, 65, 7510-7515.
10. Stoikov I.I., Galukhin A.V., Zaikov E.N., Antipin I.S. Mend. Comm. 2009, 19, 193-195.
11. Solov'eva S.E., Gruner M., Omran A.O., Gubaidullin A.T., Litvinov I.A., Habicher W.D., Antipin I.S., Konovalov A.I. Izv. Akad. Nauk, Ser. Khim. 2005, 9, 2041-2049 (in Russ.).
12. Asfari Z., Bohmer V., Harrowfeld J. M., Vicens J., Saadioui M.M. Calixarenes 2001. Dordrecht: Kluwer Academic Publisher, 2001. 683 p.
13. Štastny V., Stibor I., Dvorakova H., Lhotak P. Tetrahedron 2004, 60, 3383-3391.
14. Stoikov I.I., Omran O.A., Solovieva S.E., Latypov S.K., Enikeev K.M., Gubaidullin A.T., Antipin I.S., Konovalov A.I. Tetrahedron 2003, 59, 1469-1476.
15. Iki N., Narumi F., Fujimoto T., Morohashi N., Miyano S. J. Chem. Soc., Perkin Trans. 1998, 2, 2745-2750.
16. Gafullina L.I., Vershinina I.S., Stoikov I.I., Antipin I.S., Konovalov A.I. J. Struct. Chem. 2005, 46, 22-27.
17. Stoikov I.I., Yushkova E.A., Zhukov A.Yu., Zharov I., Antipin I.S., Konovalov A.I. Tetrahedron 2008, 64, 7112-7121.
18. Stoikov I.I., Yushkova E.A., Zhukov A.Yu., Zharov I., Antipin I.S., Konovalov A.I. Tetrahedron 2008, 64, 7489-7497.
19. Yushkova E.A., Stoikov I.I. Langmuir 2009, 25, 4919-4928.
20. Stoikov I.I., Yushkova E.A., Zharov I., Antipin I.S., Konovalov A.I. Tetrahedron 2009, 65, 7109-7114.
21. Stoikov I.I., Yushkova E.A., Bukharaev A.A., Biziaev D.A., Ziganshina S.A., Zharov I. J. Phys. Chem. C 2009, 113, 15838-15844.