Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3921
Title: The tetramerization of 2,4-dimethoxycinnamates. A novel route to calixarenes
Authors: Bruno, Botta
Paolo, Iacomacci
Cristina Di, Giovanni
Giuliano Delle, Monache
Eszter Gacs, Baitz
Botta, Maurizio 
Tafi, Andrea 
Corelli, Federico 
Domenico, Misiti
Issue Date: 1992
Project: None 
Journal: JOURNAL OF ORGANIC CHEMISTRY
Abstract: 
Treatment of (E)-2,4-dimethoxycinnamic acid methyl ester with BF3.Et2O in CHCl3 at room temperature afforded in 75% yield two stereoisomeric C-alkylcalix[4]resorcinarenes, which were shown to be in the 1,2-alternate and flattened-cone configurations.
Description: 
49254
URI: http://hdl.handle.net/20.500.12779/3921
ISSN: 0022-3263
DOI: 10.1021/jo00038a001
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