Celite Catalysed Alkylation of Alkenes
DOI:
https://doi.org/10.29356/jmcs.v49i1.1314Keywords:
Celite, heterogeneous catalysis, electrophilic substitution, Friedel-Crafts}Abstract
Abstract. In the presence of Celite mono and disubstituted alkenes could be alkylated with benzylic halides at room temperature. In order to form the C-C bond, it was necessary to use activated aromatics with alkenes or propargylic esters.
Resumen. En presencia de celita, alquenos mono- y di-sistituidos pueden ser alquilados con halogenuros de bencilo a temperatura ambiente. Para formar el enlace C-C, fue necesario usar compuestos
aromáticos activados con alquenos o ésteres propargílicos.
Downloads
References
2. Laszlo, P.; Vandormael, J. Chemistry Letters 1988, 1843-1846.
3. Rojas-Oviedo, I. Ph. D. Thesis, Medizinischen Universität zu Lübeck, Germany 1991.
4. Spange, S. Prog. Polym. Sci. 2000, 25, 781-849.
5. Neumüller, O. A. Rümps Chemie-Lexikon. Franckh´sche Verlagshandlung: Stuttgart, 1972, 522.
6. Toteva, M. M; Richard, J. P. J. Am. Chem. Soc. 1996, 118, 11434-11445.
7. Bauml, E.; Tscheschlok, K.; Pock, R.; Mayr, H. Tetrahedron Lett. 1988, 29, 6925-6926.
8. Mayr, H.; Striepe, W. J. Org. Chem. 1983, 48, 1159-1165.
9. van der Weerdt, A.J.; Cerfontain, H. Tetrahedron 1981, 37, 2121-2130.
10. Babler, J. H.; Tortorello, A. J. J. Org. Chem. 1976, 41, 885-887.
Downloads
Published
Issue
Section
License
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.