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Synthesis of Soluble Carcerands

Published online by Cambridge University Press:  31 January 2012

Jiménez-Gutiérrez I. Eddy ,
Sánchez-Montes K. Erika ,
Cortez-Maya Sandra ,
Flores-Rojas Gabriel  and
Martínez-García Marcos
Jiménez-Gutiérrez I. Eddy
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior, Coyoacán, C. P. 04510, México D. F.
Sánchez-Montes K. Erika
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior, Coyoacán, C. P. 04510, México D. F.
Cortez-Maya Sandra
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior, Coyoacán, C. P. 04510, México D. F.
Flores-Rojas Gabriel
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior, Coyoacán, C. P. 04510, México D. F.
Martínez-García Marcos
Affiliation:
Instituto de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, Circuito Exterior, Coyoacán, C. P. 04510, México D. F.
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Abstract

An efficient synthetic route for the synthesis of carcerands derived from tetramethylchlorocavitands and its tetraesters derivative were synthesized. A large-scale preparation was achieved in good yield. These carcerands are in bridging unit between oxygen atoms, i.e. contains a 3,5 dihydroxybencyl alcohol units. 1H, and 13C NMR in solution, FTIR, UV-vis spectroscopy, MS-FAB+ spectrometry and elemental analysis confirmed the structure of this carcerands.

Type
Articles
Information
MRS Online Proceedings Library (OPL) , Volume 1371: Symposium S1 – Nanostructured Materials and Nanotechnology , 2012 , imrc11-1371-s1-p147
Copyright
Copyright © Materials Research Society 2012

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References

REFERENCES

1. Kuhnert, N., Le-Gresley, A., Tetrahedron Lett. 49, 1274 (2007).Google Scholar
2. Jain, V. K., Kanaiya, P. H., Russ. Chem. Rev. 80, 75 (2011).Google Scholar
3. Liu, X., Warmuth, R., Nat. Prot. 2, 1288 (2007).Google Scholar
4. Pietraszkiewicz, M., Prus, P., Pietraszkiewicz, O., Tetrahedron. 60, 10747 (2004).Google Scholar
5. El Moll, H., Sémeril, D., Matt, D., Youinou, M., Toupet, L., Org. Biomol. Chem. 7, 495 (2009).Google Scholar
6. Dueno, E. and Bisht, K., Tetrahedron. 60, 10859 (2004).Google Scholar
7. Bradley, G. W. and Lawton, M. J. Org. Chem. 75, 8531(2010).Google Scholar