New calix[4]arenes having electron donating groups at the upper rim as molecular platforms and host molecules

Tetrahedron

Volumn 52, Issue 16, 1996, Pages 6011-6018

  Arduini, Arturo ^a   Mirone, Leonardo ^a   Paganuzzi, Daniela ^a   Pinalli, Alessandra ^a   Pochini, Andrea ^a   Secchi, Andrea ^a   Ungaro, Rocco ^a  

^a UNIVERSITY OF PARMA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CALIXARENE;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0029989549     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00238-4     Document Type: Article

References (21)

1. Gutsche, C. D. Calixarenes; Stoddart, J. F. Ed.; The Royal Society of Chemistry: Cambridge, 1989.
2. Vicens, J.; Böhmer, V., Eds. Calixarenes: a versatile Class of Macrocyclic Compounds; Kluwer Academic Publisher: Dordrecht, 1991. Böhmer, V. Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745.
3. Vicens, J.; Böhmer, V., Eds. Calixarenes: a versatile Class of Macrocyclic Compounds; Kluwer Academic Publisher: Dordrecht, 1991. Böhmer, V. Angew. Chem. Int. Ed. Engl. 1995, 34, 713-745.
4. Pochini, A.; Ungaro, R. in Comprehensive Supramolecular Chemistry, Vol. 2, Pergamon Press: Oxford, in press.
5. Verboom, W.; Durie, A.; Egberink, R. J. M.; Asfari, Z.; Reinhoudt, D. N. J. Org. Chem. 1992, 57, 1313-1316.
6. Timmerman, P.; Verboom, W.; Reinhoudt, D. N.; Arduini, A.; Grandi, S.; Sicuri, A.R.; Pochini, A.; Ungaro, R. Synthesis 1994, 185-189.
7. Arduini, A.; Fabbi, M.; Mantovani, M.; Mirone, L.; Pochini, A.; Secchi, A.; Ungaro, R. J. Org. Chem. 1995, 60, 1454-1457.
8. (a) Arduini, A.; Fanni, S.; Manfredi, G.; Pochini, A.; Ungaro, R.; Sicuri, A.R. Ugozzoli, F. J. Org. Chem. 1995, 60, 1448-1453.
9. (b) Arduini, A.; Fanni, S.; Pochini, A.; Sicuri, A.R.; Ungaro, R. Tetrahedron 1995, 51, 7951-7958.
10. Komori, T.; Shinkai, S. Chem. Lett. 1992, 901-904.
11. (a) Krow, G.R. Org. Reaction, 1993, 43, 251-798.
12. (b) Krow, G.R. in Comprehensive Organic Synthesis 1991, 7, 671-688. Pergamon Press: Oxford.
13. (c) Morita, Y.; Agawa, T. J. Org. Chem. 1992, 57, 3658-3662.
14. (d) During the preparation of this manuscript, hydroxylation of tetraalkoxycalix[4]arenes by Baeyer-Villiger oxydation of tetraalkoxycalix[4]arenes has been reported: Mascal, M.; Naven, R.T.; Warmuth, R. Tetrahedron Lett. 1995, 36, 9361-9364.
15. Yamada, A.; Murase, T.; Kikukawa, K.; Arimura, T.; Shinkai, S. J. Chem. Soc., Perkin Trans. 2 1991, 793-797.
16. Van Loon, J.D.; Verboom, W.; Reinhoudt, D.N. Org. Prep. Proc. Int. 1992, 24, 437-462
17. Arduini, A.; Cantoni, M.; Graviani, E.; Pochini, A.; Secchi, A.; Sicuri, A.R.; Ungaro, R.; Vincenti, M. Tetrahedron 1995, 51, 599-606
18. Arduini, A.; McGregor, W.M.; Paganuzzi, D.; Pochini, A.; Secchi, A.; Ungaro, R.; Ugozzoli, F. J. Chem. Soc., Perkin Trans. 2, in press.
19. Uemura, S.; Toshimitsu, A.; Okano, M. J. Chem. Soc., Perkin Trans. 1 1978, 1076-1079.
20. Very often the elemental analyses of calixarenes are uncorrect, nevertheless the identity of all new compounds reported have been proved by their spectral data. See e. g. (a) Böhmer. V.; Jung, K.; Schön, M.; Wolff, A. J. Org. Chem. 1992, 57, 790-792.
21. (b) Gutsche, C.D.; See, K.A. J. Org. Chem. 1992, 57, 4527-4539.