An efficient synthesis of pillar  - and pillar  arenes with alkyl substituents of various lengths from commercially available reagents (1,4-dialkoxybenzene and paraformaldehyde or 1,3,5-trioxane in the presence of Lewis acids) has been worked out. Cyclooligomerization products were isolated in high yields and with high oligoselectivity. In the presence of acetylcholine 1,4-bis(dodecyloxy)pillararene forms the inclusion complex in the ratio 1:1, which is observed by 1Н NMR method.
|Título traducido de la contribución||Efficient synthesis of pillararenes and pillararenes as the new synthetic acetylcholine receptors|
|Número de páginas||5|
|Estado||Published - 2013|